Patent Application
20200360386
The technology disclosed and claimed below relates generally to the field of senescent cells and their role in causing, mediating, or promoting age-related conditions. In particular, this disclosure shows how the above entitled pathways function in senescent cells, and how they can be modulated by pharmaceutical agents to improve or inhibit progression of a range of disease conditions that are often experienced in elderly patients. New p97 inhibitor structures are provided.
Senescent cells are characterized as cells that no longer have replicative capacity, but remain in the tissue of origin, eliciting a senescence-associated secretory phenotype (SASP). It is a premise of this disclosure that many age-related conditions are mediated by senescent cells, and that selective removal of the cells from tissues at or around the condition can be used clinically for the treatment of such conditions.
US 2016/0339019 A1 (Laberge et al.) describes treatment of certain age-related conditions using MDM2 inhibitors, Bcl inhibitors, and Akt inhibitors. US 20170266211 A1 (David et al.) describes the use of particular Bcl inhibitors for treatment of age-related conditions. U.S. Pat. Nos. 8,691,184, 9,096,625, and 9,403,856 (Wang et al.) describe Bcl inhibitors in a small-molecule library.
Other disclosures related to the role of senescent cells in human disease include the pre-grant publications US 2017/0056421 A1 (Zhou et al.), WO 2016/185481 (Yeda Inst.), US 2017/0216286 A1 (Kirkland et al.), and US 2017/0281649 A1 (David); and the articles by Furhmann-Stroissnigg et al. (Nat Commun. 2017 Sep. 4; 8 (1):422), Blagosklonny (Cancer Biol Ther. 2013 December; 14 (12):1092-7), and Zhu et al. (Aging Cell. 2015 August; 14 (4):644-58). The targeting of p97 to treat cancer and other conditions is referred to in Anderson et al. (Cancer Cell. 2015 Nov. 9; 28 (5):653-665) and in Segura-Cabrera et al. (Sci Rep. 2017 Mar. 21; 7:44912).
The disclosure that follows outlines a strategy for selectively eliminating senescent cells underlying certain disease processes, and provides effective compounds, pharmaceutical compositions, development strategies, and treatment protocols, and describes many of the ensuing benefits.
Certain biochemical pathways are more active in senescent cells than in other cell types. The new pathways identified as part of this invention provide a window of opportunity for targeting senescent cells without unduly impairing the activity of neighboring non-senescent cells in the target tissue. Contacting senescent cells in vitro or in vivo with small-molecule senolytic agents selectively modulates or eliminates such cells. The inhibitors can be used for administration to a target tissue in a subject, thereby selectively eliminating senescent cells in or around the tissue, and relieving one or more symptoms or signs of disease or aging that are initiated or mediated by the senescent cells.
The invention is put forth in the description that follows, in the drawings, and in the appended claims.
Senescent cell medicine encompasses the paradigm that many conditions that are associated with aging or tissue damage are caused or mediated by senescent cells. These are cells that no longer replicate, but have a secretory phenotype that includes secretion of factors that trigger pathophysiology. Senolytic agents currently in clinical development are inhibitors of Bcl family proteins or MDM2.
This disclosure shows that HSP90, PI3-kinase, proteasome, HDAC, and p97 pathways are all active in senescent cells, and can be used as an effective means for removing senescent cells from a target tissue, as an alternative to the Bcl protein family pathways and MDM2 pathways. New p97 inhibitors are provided as part of this invention. Exemplary inhibitors of the other pathways are also provided. Any of these inhibitors can be screened and developed for the treatment of conditions such as osteoarthritis, ophthalmic disease, pulmonary disease, and atherosclerosis.
Heat shock proteins (HSP) are molecular chaperones required for maintaining the stability and activity of a diverse group of client proteins, involved in cell signaling, proliferation, survival, oncogenesis and cancer progression. Inhibition of HSP alters the HSP-client protein complex, leading to reduced activity, misfolding, ubiquitination and, ultimately, proteasomal degradation of client proteins. HSPs bind and hydrolyze ATP in order to effectively regulate the maturation of client proteins through a conformationally dynamic ATPase-driven cycle with a range of co-chaperones.
HSP are upregulated under stress conditions to prevent denaturation and aggregation to maintain proteostasis. HSPs are classified according to their approximate molecular weight and include the small HSPs (Hsp27), Hsp40, Hsp60, Hsp70, Hsp90 and Hsp110.
In addition to its role as a co-chaperone of Hsp90, Hsp70 is also a powerful pro-survival protein through its inhibition of apoptosis at numerous points within the intrinsic and extrinsic cell death pathways. Several HSP protein have been implicated in the senescence response. The heat shock response is a pro-survival response in stressed cells and thus inhibition of this pathway in senescent cells is proposed as a mean of achieving senolysis.
Any HSP inhibitor currently known in the art or to be developed at a later time can be tested for senolytic activity an developed for treatment of senescence-associated conditions in accordance with this invention.
The term “EC50 μM” represents the concentration of molecule required to kill 50% of the cells. The heading “irradiated IMR90 EC50 μM” represents the potency against IMR90 cells that have been rendered senescent by irradiation. The heading “IMR90 HD EC50 μM” represents the potency against the non-senescent cells plated at high density (HD). These are cells that are not in the act of proliferation because of contact inhibition, but have not reached senescence.
For any and all of the senolytic agents put forth in this disclosure, the invention includes compounds that have an EC50 μM for irradiated IMR90 cells or HUVEC cells of less than 10, less than 1, less than 0.1, and less than 0.02 μM, and an EC50 μM of between 0.02 and 1 or between 0.02 and 0.1 μM. This invention includes compounds that have a specificity index for irradiated IMR90 cells compared with non-senescent cells or proliferating cells of at least 2, 5, 10, 50, or 200-fold.
Reference to HSP inhibitors in this application includes inhibitors of HSP90 and inhibitors of other heat shock proteins. HSP90 inhibitors are exemplary.
The phosphoinositol-3-kinase family (referred to herein as the “PI3K” or “PI3-kinase”) consist of four different classes: Class I, Class II, Class III, and Class IV. The classifications are based on primary structure, regulation, and in vitro lipid substrate specificity. Class I PI3Ks are responsible for the production of phosphatidylinositolphosphate (PI(3)P), phosphatidylinositol (3,4)-bisphosphate (PI(3,4)P2), and phosphatidylinositol (3,4,5)-trisphosphate (PI(3,4,5)P3). PI3K can be activated by G protein-coupled receptors and tyrosine kinase receptors.
Class I PI3K are heterodimeric molecules composed of a regulatory and a catalytic subunit; they are further divided between IA and IB subsets on sequence similarity. Class IA PI3K is composed of a heterodimer between a p110 catalytic subunit and a p85 regulatory subunit.
There are five variants of the p85 regulatory subunit, designated p85α, p55α, p50α, p85β, and p55γ. There are also three variants of the p110 catalytic subunit designated p110α, β, or δ catalytic subunit. The first three regulatory subunits are all splice variants of the same gene (Pik3r1), the other two being expressed by other genes (Pik3r2 and Pik3r3, p85β, and p55γ, respectively). The most highly expressed regulatory subunit is p85α; all three catalytic subunits are expressed by separate genes (Pik3ca, Pik3cb, and Pik3cd for p110α, p110β, and p110δ, respectively). The first two p110 isoforms (α and β) are expressed in all cells, but p110δ is expressed primarily in leukocytes, and it has been suggested that it evolved in parallel with the adaptive immune system. The regulatory p101 and catalytic p110γ subunits comprise the class IB PI3Ks and are encoded by a single gene each.
PI3K pathways effect cell survival via pleiotropic effects that inhibit pro-apoptotic pathways and stimulate survival pathways. Activation of PI3K leads to an inhibitory phosphorylation of propapoptotic protein BAD and BAX. PI3K pathway also inhibits FOXO family proteins which transcribe proapoptotic factors such as PUMA and BIM, thus leading to cell survival. Other pathways that are regulated by PI3K that lead to cell survival are the NFkB pathway which transcribes pro-survival genes such as Bcl-XL, Bcl-2, FLIP and IAP.
Active PI3K signaling pathways mediate cell survival. This is also the case for senescent cells and here we show that treating senescent cells with PI3K inhibitors leads to their death.
Any pI3K inhibitor currently known in the art or to be developed at a later time can be tested for senolytic activity an developed for treatment of senescence-associated conditions in accordance with this invention.
Any reference to pI3K inhibitor compounds in this disclosure may either include or exclude the following, depending on the context: perifosine (KRX-0401), idelalisib, PX-866, IPI-145, BAY 80-6946, BEZ235, RP6530, TGR 1201, SF1126, INK1117, GDC-0941, BKM120, XL147 (SAR245408), XL765 (SAR245409), Palomid 529, GSK1059615, GSK690693, ZSTK474, PWT33597, IC87114, TG100-115, CAL263, RP6503, PI-103, GNE-477, CUDC-907, AEZS-136, BYL719, BKM120, GDC-0980, GDC-0032, and MK2206.
The proteasome is a protein complex consisting of 28 subunits arranged in four stacked rings, each having 7 subunits (two outer α 1-7-rings and two inner β 1-7-rings). The catalytic protease activity derives from 3 of the β subunits. The chymotrypsin-like (CT-L) activity (β5), trypsin-like (T-L) activity (β2), and caspase-like or post-acid (PA) activity (β1).
The proteasome is the effector component of the ubiquitin-proteasome-system (UPS) where it degrades ubiquitinated proteins by proteolysis. Ubiquitination is a post-translation modification where the ubiquitin protein is covalently attached to lysine residues. A series of enzymes carries out a cascade of reactions involving E1 activating, E2 conjugating and E3 ligating enzymes. Ubiquitin itself contains lysine residues which can serve to propagate the cycle of ubiquitination with the addition of more ubiquitin units. Ubiquitination at K48 and K11 mark proteins for degradation by the proteasome. These ubiquitinated proteins marked for degradation consist of components of signaling pathways and misfolded or damaged proteins.
The UPS pathway is important for replenishing cells with amino acids required for survival. Reduced levels of proteasome have been observed in senescent cells with corresponding increases in levels of both damaged (oxidized) and ubiquitinated proteins. Several proteins involved in survival and apoptotic pathways are regulated via the UPS system. Senescent cells have a dysregulated survival/apoptosis balance, proteasome inhibition is proposed to be senolytic.
Any proteasome inhibitor currently known in the art or to be developed at a later time can be tested for senolytic activity an developed for treatment of senescence-associated conditions in accordance with this invention.
Epigenetic modifications, such as histone acetylation, are one mechanism by which gene transcription is controlled. Generally, the chromatin structure can be modulated by acetylation leading to gene transcription, or inhibition of transcription. The extent of histone acetylation is a balance between the activity of histone acetyl transferase (HAT), and histone deacetylase (HDAC).
HDACs catalyze the removal of acetyl groups from the lysine residues of histones, as well as non-histone proteins and therefore are an epigenetic modifier. HDACs regulate cellular functions such as gene expression, differentiation, proliferation and survival via the deacetylation of histone proteins.
In addition to their location in the nucleus, some HDACs can also be found in the cytoplasm and in the mitochondria. HDACs can also modulate the activity of a number of proteins via deacetylation. This includes proteins involved in apoptosis pathways.
Major chromatin landscape changes occur in senescent cells suggesting a change in the balance between HDAC and HAT activities. Therefore, protein hyperacetylation as mediated by HDAC inhibition is proposed as a means of eliminating senescent cells by inhibition of senescent cell pro-survival pathways.
Any HDAC inhibitor currently known in the art or to be developed at a later time can be tested for senolytic activity an developed for treatment of senescence-associated conditions in accordance with this invention.
p97 is a member of the superfamily of AAA+ (ATPases associated with diverse cellular activities). Proteins belonging to this family are molecular chaperones that serve major roles in cellular protein quality control, in DNA replication, transcription, recombination and repair, in membrane fusion, in movement of intracellular cargo, and in cell cycle regulation. The acquired energy from binding and hydrolysis of ATP induces a series of conformational changes and enables these AAA+ enzymes to modulate their substrates.
p97 functions to segregate protein molecules from large cellular structures such as protein assemblies, organelle membranes and chromatin, and thus facilitate the degradation of released polypeptides by the multi-subunit protease proteasome. By virtue of stabilizing p53, p97 also plays a role in the induction of senescence. p97 has been implicated in the endoplasmic reticulum associated degradation pathway (ERAD). Proteotoxic endoplasmic reticulum stress leads to the ubiquitination of misfolded proteins and these are recognized by p97 and transported to the cytosol where they are degraded by the UPS.
Changes in the endoplasmic reticulum ultrastructure have been observed in senescent cells associated with activation of the ERAD machinery. Senescent cells are therefore thought to be susceptible to the inhibition of the p97 mediated proteostasis pathway as a means of inducing apoptosis via endoplasmic reticulum stress.
Any p97 inhibitor currently known in the art or to be developed at a later time can be tested for senolytic activity an developed for treatment of senescence-associated conditions in accordance with this invention.
Many of the new p97 inhibitor compounds of this invention can be characterized as having a core 4-amino-pyrimidine ring system that is further substituted at the 2-position with a nitrogen atom of an amino substituent or a N-heterocycle. The 4-amino substituent of the core ring system can be covalently linked to a substituted phenyl group. The core ring system of these p97 inhibitors can be further substituted to provide or enhance a desirable biological or physical property.
The invention can be practiced with a compound depicted by Formula (I):
where:
R1 and R2 are independently selected from H, aryl, substituted aryl, heteroaryl and substituted heteroaryl, or R1 and R2 are cyclically linked to provide a fused 6-membered ring selected from heterocycloalkyl, substituted heterocycloalkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl and substituted heteroaryl;
R3 and R4 are independently selected from H, alkyl, substituted alkyl, alkanoyl and substituted alkanoyl, or R3 and R4 are cyclically linked and together with the nitrogen atom through which they are connected provide a ring system selected from heterocycloalkyl, substituted heterocycloalkyl, heteroaryl and substituted heteroaryl;
R5 is selected from H, alkyl and substituted alkyl;
L is a covalent bond or a linker;
R6 is selected from H, amino, substituted amino and electrophilic reactive group (e.g., a substituent comprising 2-chloro-acetyl (—COCH2Cl), vinyl sulfone (—SO2CH═CH2), acetylene or methyl-acetylene, i.e., cysteine-reactive groups);
each R7 is independently selected from hydrogen, halogen, acyl, amino, substituted amino, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, substituted heterocycloalkyl, alkylcarboxy, aminoalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, arylalkyl, substituted arylalkyl, arylcycloalkyl, substituted arylcycloalkyl, heteroarylalkyl, substituted heteroarylalkyl, cyano, hydroxyl, alkoxy, substituted alkoxy, nitro, alkanoyl, substituted alkanoyl, acyloxy and aryloxy; and
n is 0 to 4.
This disclosure includes p97 inhibitors of Formula (I), where R5 is H. In the p97 inhibitors of this disclosure, L can be any divalent group suitable to covalently link the 4-amino nitrogen to the appended phenyl group. Sometimes L is a covalent bond that directly links the two groups. Alternatively, L can be a linear linker of 1-6 atoms in length, such as a C(1-6) alkyl or substituted C(1-6) alkyl. It is understood that one or more carbon atoms of the backbone of such a linear linker can be replaced with a heteroatom (e.g., N, O or S). In addition, a variety of linking functional groups (e.g., —CONH—, —SO2NH—, —COO—, SO2, CO, —O— or —NH—) can be incorporated into the linker L, e.g., to provide for a connection to the 4-amino and/or the phenyl ring.
The p97 inhibitors of Formula (I) can be further described by Formula (II):
where Z1 and Z2 are independently selected from O, S, NR11 and C(R11)2; and R11 is selected from H, alkyl, substituted alkyl, alkanoyl, substituted alkanoyl, alkylsulfonyl and substituted alkylsulfonyl.
This disclosure includes p97 inhibitors of Formula (II), where R3 and R4 are cyclically linked and together with the nitrogen atom through which they are connected provide a ring system selected from heterocycloalkyl, substituted heterocycloalkyl, heteroaryl and substituted heteroaryl. Sometimes, R3 and R4 can be cyclically linked to provide indole or substituted indole. This disclosure includes p97 inhibitors of Formula (II), where R5 is H.
As such, the p97 inhibitors of Formula (II) can be further described by Formula (III):
where m is 0-3 (e.g., 1 or 2); R12, R13 and each R14 is independently selected from hydrogen, halogen, acyl, amino, substituted amino, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, substituted heterocycloalkyl, alkylcarboxy, aminoalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, arylalkyl, substituted arylalkyl, arylcycloalkyl, substituted arylcycloalkyl, heteroarylalkyl, substituted heteroarylalkyl, cyano, hydroxyl, alkoxy, substituted alkoxy, nitro, alkanoyl, substituted alkanoyl, acyloxy and aryloxy; and n is 0 to 4.
This disclosure includes compounds of Formula (III) where Z1 is CH2; and Z2 is NR11, wherein R11 is selected from H, alkyl, substituted alkyl, alkanoyl and substituted alkanoyl. Alternatively, Z1 is NR11, wherein R11 is selected from H, alkyl, substituted alkyl, alkanoyl and substituted alkanoyl; and Z2 is CH2. Sometimes, the R11 group is H or one of the following structures:
where:
R21 and R22 are independently selected from H, alkyl, substituted alkyl, alkanoyl and substituted alkanoyl, or R21 and R22 are cyclically linked and together with the nitrogen atom through which they are connected provide a ring system selected from heterocycloalkyl, substituted heterocycloalkyl, heteroaryl and substituted heteroaryl;
R23 and R24 are independently selected from H, alkyl, substituted alkyl; and
r is 1-12 (e.g., 1-8 or 16, such as 1, 2, 3, 4, 5 or 6).
In the p97 inhibitors of this disclosure (such as Formulae (I) to (III)), R6 can be H. In addition, m can be 1. This disclosure provides p97 inhibitors having a 2-substituent of the core ring system (particularly —NR3R4) that can have one of the following Formulae:
where R12 is selected from H, alkyl and substituted alkyl; and R′ and R″ are independently selected from H, alkyl and substituted alkyl, or R′ and R″ are cyclically linked and together with the nitrogen atom through which they are connected provide a heterocycloalkyl or substituted heterocycloalkyl.
Exemplary p97 inhibitors of this disclosure having such a 2-substituent of the core ring system are shown below:
This disclosure includes compounds of Formula (II) or (III), where Z1 or Z2 is O. When one of Z1 or Z2 is O then the other of Z1 or Z2 can be CH2. As such, this disclosure includes p97 inhibitors having a dihydropyran ring fused to the pyrimidine of the core ring system. Sometimes, when Z1 or Z2 is O, the R6 substituent of the appended phenyl group is not H. Rather R6 can be a substituent including reactive electrophilic group.
This disclosure includes compounds (including Formulas (I) to (III)) that include a R6 substituent which is a reactive electrophilic group. A reactive electrophilic group is a electrophilic functional group that is capable of reacting with a functional group of a target peptide or protein, such as a nucleophilic sidechain group of an amino acid residue of the target peptide or protein. In general, the reactive electrophilic group is biocompatible with an aqueous or physiological environment and selectively reacts with a nucleophilic group of the target protein once binding has occurred.
A variety of reactive function groups can be adapted for use in the p97 inhibitors of this invention, including reactive function groups found in reversible and irreversible mechanism-based inactivators. See e.g., Chapter 5, pages 207-265 of “Enzyme Inhibition and Inactivation” in “The organic chemistry of drug design and drug action” by Silverman and Holladay, Third Ed. Academic Press, 2014. For example, reactive electrophilic groups that find use in the p97 inhibitors of this disclosure include 2-chloro-acetyl (—COCH2Cl), vinyl sulfone (—SO2CH═CH2), acetylene or methyl-acetylene (i.e., cysteine-reactive groups).
As such, this disclosure includes p97 inhibitors having a R6 substituent that can be a substituted amino and include a reactive electrophilic group, such as 2-chloro-acetamide (—NHCOCH2Cl), vinyl sulfonamide (—NHSO2CH═CH2), acetylene or methyl-acetylene. Alternatively, R6 can be H. Sometimes, R6 is selected from —NHCOCH2Cl, —SO2CH═CH2—NHCOCH═CH2, —CCH and —CCMe.
This disclosure includes p97 inhibitors having a 2-substituent of the core ring system (particularly —NR3R4) that is of one of the following Formulae:
where R12 is selected from H, alkyl and substituted alkyl; and R′ and R″ are independently selected from H, alkyl and substituted alkyl, or R′ and R″ are cyclically linked and together with the nitrogen atom through which they are connected provide a heterocycloalkyl or substituted heterocycloalkyl.
Exemplary p97 inhibitors of this disclosure having such a 2-substituent of the core ring system and a reactive electrophilic group are shown below:
The p97 inhibitors of Formula (I) can be further described by Formula (IV):
wherein R2 is selected from aryl, substituted aryl, heteroaryl and substituted heteroaryl.
This disclosure includes p97 inhibitors of Formula (IV), where R2 is a 5-6 fused bicyclic heteroaryl or substituted 5-6 fused bicyclic heteroaryl. As such, R2 can be of the Formula:
where:
Z3 is selected from O, S and NR10;
R10 is selected from H, alkyl and substituted alkyl;
R8 and each R9 are independently selected from hydrogen, halogen, acyl, amino, substituted amino, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, substituted heterocycloalkyl, alkylcarboxy, aminoalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, arylalkyl, substituted arylalkyl, arylcycloalkyl, substituted arylcycloalkyl, heteroarylalkyl, substituted heteroarylalkyl, cyano, hydroxyl, alkoxy, substituted alkoxy, nitro, alkanoyl, substituted alkanoyl, acyloxy and aryloxy; and p is 0 to 4.
This disclosure includes p97 inhibitors of Formula (IV), where R3 and R4 are independently selected from H, alkyl, substituted alkyl, alkanoyl and substituted alkanoyl. As such, the p97 inhibitors of Formula (IV) can be further described by Formula (IVb):
where: Y is selected from cycloalkyl, substituted cycloalkyl, heterocycloalkyl, substituted heterocycloalkyl, aryl, substituted aryl, heteroaryl and substituted heteroaryl; R3 is selected from H, alkyl and substituted alkyl; m2 is 1-3 (e.g., 1 or 2); and m1 is 0-3 (e.g., 1 or 2).
An exemplary p97 inhibitor of this disclosure having such structure is shown below:
The compounds referred to above and depicted in the drawings can be screened on the molecular level for their ability to perform in a way that indicate that they are candidate agents for use according to this invention. For example, compounds can be tested in molecular assays for their ability to inhibit protein activity for any of the entitled pathways. Example 1 provides illustrations of assays for this purpose.
Alternatively or in addition, compounds can be screened for an ability to kill senescent cells specifically. Cultured cells are contacted with the compound, and the degree of cytotoxicity or inhibition of the cells is determined. The ability of the compound to kill or inhibit senescent cells can be compared with the effect of the compound on normal cells that are freely dividing at low density, and normal cells that are in a quiescent state at high density. Examples 2 and 3 provide illustrations of senescent cell killing using the human target tissue fibroblast IMR90 cell line and HUVEC cells. Similar protocols are known and can be developed or optimized for testing the ability of the cells to kill or inhibit other senescent cells and other cell types, such as cancer cells.
Candidate senolytic agents according to this invention that are effective in selectively killing senescent cells in vitro can be further screened in animal models for particular disease. Examples 4, 5, 6, and 7 below provide illustrations for osteoarthritis, eye disease, lung disease, and atherosclerosis, respectively.
Preparation and Formulation of pharmaceutical agents for use according to this invention can incorporate standard technology, as described, for example, in the current edition of Remington: The Science and Practice of Pharmacy. The Formulation will typically be optimized for administration to the target tissue, for example, by local administration, in a manner that enhances access of the active agent to the target senolytic cells and providing the optimal duration of effect, while minimizing side effects or exposure to tissues that are not involved in the condition being treated.
Pharmaceutical preparations for use in treating senescence-related conditions and other diseases can be prepared by mixing a senolytic agent with a pharmaceutically acceptable base or carrier and as needed one or more pharmaceutically acceptable excipients. Exemplary excipients and additives that can be used include surfactants (for example, polyoxyethylene and block copolymers); buffers and pH adjusting agents (for example, hydrochloric acid, sodium hydroxide, phosphate, citrate, and sodium cyanide); tonicity agents (for example, sodium bisulfite, sodium sulfite, glycerin, and propylene glycol); and chelating agents (for example, ascorbic acid, sodium edetate, and citric acid).
Depending on the target tissue, it may be appropriate to Formulate the pharmaceutical composition for sustained or timed release. Oral timed release Formulations may include a mixture of isomeric variants, binding agents, or coatings. Injectable time release Formulations may include the active agent in combination with a binding agent, encapsulating agent, or microparticle. For treatment of joint diseases such as osteoarthritis, the pharmaceutical composition is typically Formulated for intra-articular administration. For treatment of eye disease such as glaucoma (POAG), diabetic retinopathy (DR) or age-related macular degeneration (AMD), the composition may be Formulated for intravitreal or intracameral administration. For treatment of lung diseases, the composition may be Formulated as an aerosol, or for intratracheal administration.
This invention provides commercial products that are kits that enclose unit doses of one or more of the agents or compositions described in this disclosure. Such kits typically comprise a pharmaceutical preparation in one or more containers. The preparations may be provided as one or more unit doses (either combined or separate). The kit may contain a device such as a syringe for administration of the agent or composition in or around the target tissue of a subject in need thereof. The product may also contain or be accompanied by an informational package insert describing the use and attendant benefits of the drugs in treating the senescent cell associated condition, and optionally an appliance or device for delivery of the composition.
Senescent cells accumulate with age, which is why conditions mediated by senescent cells occur more frequently in older adults. In addition, different types of stress on pulmonary tissues may promote the emergence of senescent cells and the phenotype they express. Cell stressors include oxidative stress, metabolic stress, DNA damage (for example, as a result of environmental ultraviolet light exposure or genetic disorder), oncogene activation, and telomere shortening (resulting, for example, from hyperproliferation). Tissues that are subject to such stressors may have a higher prevalence of senescent cells, which in turn may lead to presentation of certain conditions at an earlier age, or in a more severe form. An inheritable susceptibility to certain conditions suggests that the accumulation of disease-mediating senescent cells may directly or indirectly be influenced by genetic components, which can lead to earlier presentation.
One of the benefits of the senescent cell paradigm is that successful removal of senescent cells may provide the subject with a long-term therapeutic effect. Senescent cells are essentially non-proliferative, which means that subsequent repopulation of a tissue with more senescent cells can only occur by conversion of non-senescent cells in the tissue to senescent cells—a process that takes considerably longer than simple proliferation. As a general principle, a period of therapy with a senolytic agent of this invention that is sufficient to remove senescent cells from a target tissue (a single dose, or a plurality of doses given, for example, every day, semi weekly, or weekly, given over a period of a few days, a week, or several months) may provide the subject with a period of efficacy (for example, for two weeks, a month, two months, or more) during which the senolytic agent is not administered, and the subject experiences alleviation, reduction, or reversal of one or more adverse signs or symptoms of the condition being treated.
To treat a particular senescence-related condition with a senolytic agent according to this invention, the therapeutic regimen will depend on the location of the senescent cells, and the pathophysiology of the disease.
The senolytic agents of this invention can be used for prevention or treatment of various senescence-related conditions. Such conditions will typically (although not necessarily) characterized by an overabundance of senescent cells (such as cells expressing p16 and other senescence markers) in or around the site of the condition, or an overabundance of expression of p16 and other senescence markers, in comparison with the frequency of such cells or the level of such expression in unaffected tissue. Non-limiting examples of current interest include the treatment of osteoarthritis, eye disease, lung disease, and atherosclerosis as illustrated in the following sections.
The senolytic agents listed in this disclosure can be developed for treating osteoarthritis, or for selectively eliminating senescent cells in or around a joint of a subject in need thereof, including but not limited to a joint affected by osteoarthritis.
Osteoarthritis degenerative joint disease is characterized by fibrillation of the cartilage at sites of high mechanical stress, bone sclerosis, and thickening of the synovium and the joint capsule. Fibrillation is a local surface disorganization involving splitting of the superficial layers of the cartilage. The early splitting is tangential with the cartilage surface, following the axes of the predominant collagen bundles. Collagen within the cartilage becomes disorganized, and proteoglycans are lost from the cartilage surface. In the absence of protective and lubricating effects of proteoglycans in a joint, collagen fibers become susceptible to degradation, and mechanical destruction ensues. Predisposing risk factors for developing osteoarthritis include increasing age, obesity, previous joint injury, overuse of the joint, weak thigh muscles, and genetics. Symptoms of osteoarthritis include sore or stiff joints, particularly the hips, knees, and lower back, after inactivity or overuse; stiffness after resting that goes away after movement; and pain that is worse after activity or toward the end of the day.
Compounds according to this invention can be used to reduce or inhibit loss or erosion of proteoglycan layers in a joint, reduces inflammation in the affected joint, and promotes, stimulates, enhances, or induces production of collagen, for example, type 2 collagen. The compound may causes a reduction in the amount, or level, of inflammatory cytokines, such as IL-6, produced in a joint and inflammation is reduced. The compounds can be used for treating osteoarthritis and/or inducing collagen, for example, Type 2 collagen, production in the joint of a subject. A compound also can be used for decreasing, inhibiting, or reducing production of metalloproteinase 13 (MMP-13), which degrades collagen in a joint, and for restoring proteoglycan layer or inhibiting loss and/or degradation of the proteoglycan layer.
Potential benefits of treatment with a senolytic agent according to this invention include inhibiting or reversing cartilage or bone erosion. The senolytic compound may restore or inhibit deterioration of strength of a join, or reduce joint pain.
The senolytic agents listed in this disclosure can be used for preventing or treating an adverse ophthalmic condition in a subject in need thereof by removing senescent cells in or around an eye of the subject, whereby at least one sign or symptom of the disease is decreased in severity. Such conditions include both back-of-the-eye diseases, and front-of-the-eye diseases. The senolytic agents listed in this disclosure can be developed for selectively eliminating senescent cells in or around ocular tissue in a subject in need thereof.
Diseases of the eye that can be treated according to this invention include presbyopia, macular degeneration (including wet or dry AMD), diabetic retinopathy, and glaucoma.
Macular degeneration is a neurodegenerative condition that can be characterized as a back-of-the-eye disease, It causes the loss of photoreceptor cells in the central part of retina, called the macula. Macular degeneration can be dry or wet. The dry form is more common than the wet, with about 90% of age-related macular degeneration (AMD) patients diagnosed with the dry form. The wet form of the disease can lead to more serious vision loss. Age and certain genetic factors and environmental factors can be risk factors for developing AMD. Environmental factors include, for example, omega-3 fatty acids intake, estrogen exposure, and increased serum levels of vitamin D. Genetic risk factors can include, for example, reduced ocular Dicer1 levels, and decreased micro RNAs, and DICER1 ablation.
Dry AMD is associated with atrophy of the retinal pigment epithelium (RPE) layer, which causes loss of photoreceptor cells. The dry form of AMD can result from aging and thinning of macular tissues and from deposition of pigment in the macula. With wet AMD, new blood vessels can grow beneath the retina and leak blood and fluid. Abnormally leaky choroidal neovascularization can cause the retinal cells to die, creating blind spots in central vision. Different forms of macular degeneration can also occur in younger patients. Non-age related etiology can be linked to, for example, heredity, diabetes, nutritional deficits, head injury, or infection.
The formation of exudates, or “drusen,” underneath the Bruch's membrane of the macula is can be a physical sign that macular degeneration can develop. Symptoms of macular degeneration include, for example, perceived distortion of straight lines and, in some cases, the center of vision appears more distorted than the rest of a scene; a dark, blurry area or “white-out” appears in the center of vision; or color perception changes or diminishes.
Another back-of-the-eye disease is diabetic retinopathy (DR). According to Wikipedia, the first stage of DR is non-proliferative, and typically has no substantial symptoms or signs. NPDR is detectable by fundus photography, in which microaneurysms (microscopic blood-filled bulges in the artery walls) can be seen. If there is reduced vision, fluorescein angiography can be done to see the back of the eye. Narrowing or blocked retinal blood vessels can be seen clearly and this is called retinal ischemia (lack of blood flow). Macular edema in which blood vessels leak their contents into the macular region can occur at any stage of NPDR. The symptoms of macular edema are blurred vision and darkened or distorted images that are not the same in both eyes. Ten percent (10%) of diabetic patients will have vision loss related to macular edema. Optical Coherence Tomography can show the areas of retinal thickening (due to fluid accumulation) of macular edema.
In the second stage of DR, abnormal new blood vessels (neovascularization) form at the back of the eye as part of proliferative diabetic retinopathy (PDR); these can burst and bleed (vitreous hemorrhage) and blur the vision, because these new blood vessels are fragile. The first time this bleeding occurs, it may not be very severe. In most cases, it will leave just a few specks of blood, or spots floating in a person's visual field, though the spots often go away after few hours. These spots are often followed within a few days or weeks by a much greater leakage of blood, which blurs the vision. In extreme cases, a person may only be able to tell light from dark in that eye. It may take the blood anywhere from a few days to months or even years to clear from the inside of the eye, and in some cases the blood will not clear. These types of large hemorrhages tend to happen more than once, often during sleep. On funduscopic exam, a doctor will see cotton wool spots, flame hemorrhages (similar lesions are also caused by the alpha-toxin of Clostridium novyi), and dot-blot hemorrhages.
Presbyopia is an age-related condition where the eye exhibits a progressively diminished ability to focus on near objects as the speed and amplitude of accommodation of a normal eye decreases with advancing age. Loss of elasticity of the crystalline lens and loss of contractility of the ciliary muscles can cause presbyopia. Age-related changes in the mechanical properties of the anterior lens capsule and posterior lens capsule suggest that the mechanical strength of the posterior lens capsule decreases significantly with age. The laminated structure of the capsule of the eye also changes and can result, at least in part, from a change in the composition of the tissue.
Compounds provided by this disclosure can slow the disorganization of the type IV collagen network, decrease or inhibit epithelial cell migration and can also delay the onset of presbyopia or decrease or slow the progressive severity of the condition. They can also be useful for post-cataract surgery to reduce the likelihood of occurrence of PCO.
Another condition treatable with senolytic agents is glaucoma. Normally, clear fluid flows into and out of the front part of the eye, known as the anterior chamber. In individuals who have open/wide-angle glaucoma, the clear fluid drains too slowly, leading to increased pressure within the eye. If left untreated, the high pressure in the eye can subsequently damage the optic nerve and can lead to complete blindness. The loss of peripheral vision is caused by the death of ganglion cells in the retina. The effect of a therapy on inhibiting progression of glaucoma can be monitored by automated perimetry, gonioscopy, imaging technology, scanning laser tomography, HRT3, laser polarimetry, GDX, ocular coherence tomography, ophthalmoscopy, and pachymeter measurements that determine central corneal thickness.
Ophthalmic conditions treatable with senolytic agents include ischemic or vascular conditions, such as diabetic retinopathy, glaucomatous retinopathy, ischemic arteritic optic neuropathies, and vascular diseases characterized by arterial and venous occlusion, retinopathy of prematurity and sickle cell retinopathy.
Ophthalmic conditions treatable with senolytic agents include degenerative conditions, such as dermatochalasis, ptosis, keratitis sicca, Fuch's corneal dystrophy, presbyopia, cataract, wet age related macular degeneration (wet AMD), dry age related macular degeneration (dry AMD); degenerative vitreous disorders, including vitreomacular traction (VMT) syndrome, macular hole, epiretinal membrane (ERM), retinal tears, retinal detachment, and proliferative vitreoretinopathy (PVR).
Ophthalmic conditions treatable with senolytic agents include genetic conditions, such as retinitis pigmentosa, Stargardt disease, Best disease and Leber's hereditary optic neuropathy (LHON). Ophthalmic conditions treatable with a senolytic agent in accordance with this invention include conditions caused by a bacterial, fungal, or virus infection. These include conditions caused or provoked by an etiologic agent such as herpes zoster varicella (HZV), herpes simplex, cytomegalovirus (CMV), and human immunodeficiency virus (HIV).
Ophthalmic conditions treatable with senolytic agents include inflammatory conditions, such as punctate choroiditis (PIC), multifocal choroiditis (MIC) and serpiginous choroidopathy. Ophthalmic conditions treatable with a senolytic agent in accordance with this invention also include iatrogenic conditions, such as a post-vitrectomy cataract and radiation retinopathy.
Potential benefits of treatment with a senolytic agent according to this invention include reversing or inhibiting progression of any of the aforelisted signs and symptoms of ocular diseases, such as neovascularization, vaso-obliteration, and an increase in intraocular pressure, leading to an impairment of retinal function and loss of vision.
The senolytic agents listed in this disclosure can be developed for treating pulmonary disease, or for selectively eliminating senescent cells in or around a lung of a subject in need thereof. Pulmonary conditions that can be treated according to this invention include idiopathic pulmonary fibrosis (IPF), chronic obstructive pulmonary disease (COPD), asthma, cystic fibrosis, bronchiectasis, and emphysema.
COPD is a lung disease defined by persistently poor airflow resulting from the breakdown of lung tissue, emphysema, and the dysfunction of the small airways, obstructive bronchiolitis. Primary symptoms of COPD include shortness of breath, wheezing, chest tightness, chronic cough, and excess sputum production. Elastase from cigarette smoke-activated neutrophils and macrophages can disintegrate the extracellular matrix of alveolar structures, resulting in enlarged air spaces and loss of respiratory capacity. COPD can be caused by, for example, tobacco smoke, cigarette smoke, cigar smoke, secondhand smoke, pipe smoke, occupational exposure, exposure to dust, smoke, fumes, and pollution, occurring over decades thereby implicating aging as a risk factor for developing COPD. High concentrations of free radicals in tobacco smoke can lead to cytokine release as part of an inflammatory response to irritants in the airway, resulting in damage the lungs by protease.
Symptoms of COPD can include shortness of breath, wheezing, chest tightness, having to clear one's throat first thing in the morning because of excess mucus in the lungs, a chronic cough that produces sputum that can be clear, white, yellow or greenish, cyanosis, frequent respiratory infections, lack of energy, and unintended weight loss.
Pulmonary fibrosis is a chronic and progressive lung disease characterized by stiffening and scarring of the lung, which can lead to respiratory failure, lung cancer, and heart failure. Fibrosis is associated with repair of epithelium. Fibroblasts are activated, production of extracellular matrix proteins is increased, and transdifferentiation to contractile myofibroblasts contribute to wound contraction. A provisional matrix plugs the injured epithelium and provides a scaffold for epithelial cell migration, involving an epithelial-mesenchymal transition (EMT). Blood loss associated with epithelial injury induces platelet activation, production of growth factors, and an acute inflammatory response. Normally, the epithelial barrier heals and the inflammatory response resolves. However, in fibrotic disease the fibroblast response continues, resulting in unresolved wound healing. Formation of fibroblastic foci is a feature of the disease, reflecting locations of ongoing fibrogenesis.
Subjects at risk of developing pulmonary fibrosis include, for example, those exposed to environmental or occupational pollutants, such as asbestosis and silicosis; those who smoke cigarettes; those who have a connective tissue diseases such as RA, SLE, scleroderma, sarcoidosis, or Wegener's granulomatosis; those who have infections; those who take certain medications, including, for example, amiodarone, bleomycin, busufan, methotrexate, and nitrofurantoin; those subject to radiation therapy to the chest; and those whose family member have pulmonary fibrosis.
Other pulmonary conditions that can be treated by using a compound according to this invention include emphysema, asthma, bronchiectasis, and cystic fibrosis. Pulmonary diseases can also be exacerbated by tobacco smoke, occupational exposure to dust, smoke, or fumes, infection, or pollutants that contribute to inflammation.
Bronchiectasis can result from damage to the airways that causes them to widen and become flabby and scarred. Bronchiectasis can be caused by a medical condition that injures the airway walls or inhibits the airways from clearing mucus. Examples of such conditions include cystic fibrosis and primary ciliary dyskinesia (PCD). When only one part of the lung is affected, the disorder can be caused by a blockage rather than a medical condition.
The methods of this invention for treating or reducing the likelihood of a pulmonary condition can also be used for treating a subject who is aging and has loss of pulmonary function, or degeneration of pulmonary tissue. Effects of treatment can be determined using techniques that evaluate mechanical functioning of the lung, for example, techniques that measure lung capacitance, elastance, and airway hypersensitivity can be performed. For example, expiratory reserve volume (ERV), forced vital capacity (FVC), forced expiratory volume (FEV) (e.g., FEV in one second, FEV1), FEV1/FEV ratio, forced expiratory flow 25% to 75%, and maximum voluntary ventilation (MVV), peak expiratory flow (PEF), slow vital capacity (SVC) can be measured. Peripheral capillary oxygen saturation (SpO2) can also be measured; normal oxygen levels are typically between 95% and 100%. An SpO2 level below 90% indicates that the subject has hypoxemia.
Potential benefits of treatment with a senolytic agent according to this invention include include alleviating or halting progression of one or more signs or symptoms of the condition being treated, as indicated above. Objectives may include increasing lung volume or capacity, and manifestations thereof such as improving oxygen saturation.
The senolytic compounds of this invention can be used for the treatment of atherosclerosis: for example, by inhibiting formation, enlargement, or progression of atherosclerotic plaques in a subject. The senolytic compounds of this invention can also be used to enhance stability of atherosclerotic plaques that are present in one or more blood vessels of a subject, thereby inhibiting them from rupturing and occluding the vessels.
Atherosclerosis is characterized by patchy intimal plaques, atheromas, that encroach on the lumen of medium-sized and large arteries; the plaques contain lipids, inflammatory cells, smooth muscle cells, and connective tissue. Atherosclerosis can affect large and medium-sized arteries, including the coronary, carotid, and cerebral arteries, the aorta and branches thereof, and major arteries of the extremities.
Atherosclerosis may lead to an increase in artery wall thickens. Symptoms develop when growth or rupture of the plaque reduces or obstructs blood flow; and the symptoms can vary depending on which artery is affected. Atherosclerotic plaques can be stable or unstable. Stable plaques regress, remain static, or grow slowly, sometimes over several decades, until they can cause stenosis or occlusion. Unstable plaques are vulnerable to spontaneous erosion, fissure, or rupture, causing acute thrombosis, occlusion, and infarction long before they cause hemodynamically significant stenosis. Clinical events can result from unstable plaques, which do not appear severe on angiography; thus, plaque stabilization can be a way to reduce morbidity and mortality. Plaque rupture or erosion can lead to major cardiovascular events such as acute coronary syndrome and stroke. Disrupted plaques can have a greater content of lipid, macrophages, and have a thinner fibrous cap than intact plaques.
Atherosclerosis is thought to be due in significant part to a chronic inflammatory response of white blood cells in the walls of arteries. This is promoted by low-density lipoproteins (LDL), plasma proteins that carry cholesterol and triglycerides, in the absence of adequate removal of fats and cholesterol from macrophages by functional high-density lipoproteins (HDL). The earliest visible lesion of atherosclerosis is the “fatty streak,” which is an accumulation of lipid-laden foam cells in the intimal layer of the artery. The hallmark of atherosclerosis is atherosclerotic
Diagnosis of atherosclerosis and other cardiovascular disease can be based on symptoms, for example, angina, chest pressure, numbness or weakness in arms or legs, difficulty speaking or slurred speech, drooping muscles in face, leg pain, high blood pressure, kidney failure and/or erectile dysfunction, medical history, and/or physical examination of a patient. Diagnosis can be confirmed by angiography, ultrasonography, or other imaging tests. Subjects at risk of developing cardiovascular disease include those having any one or more of predisposing factors, such as a family history of cardiovascular disease and those having other risk factors, for example, predisposing factors including high blood pressure, dyslipidemia, high cholesterol, diabetes, obesity and cigarette smoking, sedentary lifestyle, and hypertension. The condition can be assessed, for example, by angiography, electrocardiography, or stress test.
Potential benefits of treatment with a senolytic agent according to this invention include alleviating or halting progression of one or more signs or symptoms of the condition, such as the frequency of plaques, the surface area of vessels covered by plaques, angina, and reduced exercise tolerance.
A “senescent cell” is generally thought to be derived from a cell type that typically replicates, but as a result of aging or other event that causes a change in cell state, can no longer replicate. For the purpose of practicing aspects of this invention, senescent cells can be identified as expressing p16, or at least one marker selected from p16, senescence-associated β-galactosidase, and lipofuscin; sometimes two or more of these markers, and other markers of the senescence-associated secretory profile (SASP) such as but not limited to interleukin 6, and inflammatory, angiogenic and extracellular matrix modifying proteins. Unless explicitly stated otherwise, the senescent cells referred to in the claims do not include cancer cells.
A “senescence associated”, “senescence related” or “age related” disease, disorder, or condition is a physiological condition that presents with one or more symptoms or signs that are adverse to the subject. The condition is “senescence associated” if it is “caused or mediated at least in part by senescent cells.” This means that at least one component of the SASP in or around the affected tissue plays a role in the pathophysiology of the condition such that elimination of at least some of the senescent cells in the affected tissue results in substantial relief or lessening of the adverse symptoms or signs, to the patient's benefit. Senescence associated disorders that can potentially be treated or managed using the methods and products of this invention include disorders referred to in this disclosure and in previous disclosures referred to in the discussion. Unless explicitly stated otherwise, the term does not include cancer.
An inhibitor of “protein function” is a compound that to a substantial degree prevents the target protein already expressed in a target cell from performing an enzymatic, binding, or regulatory function that it normally performs in the target cell. This results in elimination of the target cell or rendering the cell more susceptible to the toxicity of another compound or event.
A compound, composition or agent is typically referred to as “senolytic” if it eliminates senescent cells, compared with replicative cells of the same tissue type, or quiescent cells lacking SASP markers. Alternatively or in addition, a compound or combination may effectively be used according to this invention if it decreases the release of pathological soluble factors or mediators as part of the senescence associated secretory phenotype that play a role in the initial presentation or ongoing pathology of a condition, or inhibit its resolution. In this respect, the term “senolytic” refers to functional inhibition, such that compounds that work primarily by inhibiting rather than eliminating senescent cells (senescent cell inhibitors) can be used in a similar fashion with ensuing benefits.
Selective removal or “elimination” of senescent cells from a mixed cell population or tissue doesn't require that all cells bearing a senescence phenotype be removed: only that the proportion of senescent cells initially in the tissue that remain after treatment is substantially higher than the proportion of non-senescent cells initially in the tissue that remain after the treatment.
Successful “treatment” of a condition according to this invention may have any effect that is beneficial to the subject being treated. This includes decreasing severity, duration, or progression of a condition, or of any adverse signs or symptoms resulting therefrom. In some circumstances, senolytic agents can also be used to prevent or inhibit presentation of a condition for which a subject is susceptible, for example, because of an inherited susceptibility of because of medical history.
A “therapeutically effective amount” is an amount of a compound of the present disclosure that (i) treats the particular disease, condition, or disorder, (ii) attenuates, ameliorates, or eliminates one or more symptoms of the particular disease, condition, or disorder, (iii) prevents or delays the onset of one or more symptoms of the particular disease, condition, or disorder described herein, (iv) prevents or delays progression of the particular disease, condition or disorder, (v) at least partially reverses damage caused by the condition prior to treatment; or has a plurality of such effects in any combination.
A “phosphorylated” form of a compound is a compound which bears one or more phosphate groups covalently bound to the core structure through an oxygen atom, which was typically but not necessarily present on the molecule before phosphorylation. For example, one or more —OH or —COOH groups may have been substituted in place of the hydrogen with a phosphate group which is either —OPO3H2 or —CnPO3H2 (where n is 1 to 4). In some phosphorylated forms, the phosphate group may be removed in vivo (for example, by enzymolysis), in which case the phosphorylated form may be a pro-drug of the non-phosphorylated form. A non-phosphorylated form has no such phosphate group. A dephosphorylated form is a phosphorylated molecule after at least one phosphate group has been removed.
“Small molecule” senolytic agents according to this invention have molecular weights less than 20,000 daltons, and are often less than 10,000, 5,000, or 2,000 daltons. Small molecule inhibitors are not antibody molecules or oligonucleotides, and typically have no more than five hydrogen bond donors (the total number of nitrogen-hydrogen and oxygen-hydrogen bonds), and no more than 10 hydrogen bond acceptors that are nitrogen or oxygen atoms.
Unless otherwise stated or required, each of the compound structures referred to in the invention include conjugate acids and bases having the same structure, crystalline and amorphous forms of those compounds, pharmaceutically acceptable salts, and prodrugs. This includes, for example, tautomers, polymorphs, solvates, hydrates, unsolvated polymorphs (including anhydrates). The compound may be any stereoisomer of the structure shown, or a mixture thereof, unless a particular stereoisomer or a particular chiral structure is explicitly referred to.
Unless otherwise stated or implied, the term “substituted” when used to modify a specified group or radical means that one or more hydrogen atoms of the specified group or radical are each independently replaced with the same or different substituent groups which is not hydrogen. Unless indicated otherwise, the nomenclature of substituents is arrived at by naming the terminal portion of the functionality followed by the adjacent functionality toward the point of attachment. For example, the substituent “arylalkyloxycarbonyl” refers to the group (aryl)-(alkyl)-O—C(O)—.
A “linker” is a moiety that covalently connects two or more chemical structures, and has a backbone of 100 atoms or less in length between the two structures. The linker may be cleavable or non-cleavable. The linker typically has a backbone of between 1 and 20 or between 1 and 100 atoms in length, in linear or branched form. The bonds between backbone atoms may be saturated or unsaturated. The linker backbone may include a cyclic group, for example, an optionally substituted aryl, heteroaryl, heterocycle or cycloalkyl group.
Except where otherwise stated or required, other terms used in the specification have their ordinary meaning.
For all purposes in the United States and in other jurisdictions where effective, each and every publication and patent document cited in this disclosure is hereby incorporated herein by reference in its entirety for all purposes to the same extent as if each such publication or document was specifically and individually indicated to be incorporated herein by reference.
Depending on the implementation, a referral to inhibitors of the five pathways newly discovered in this application may or may not include one or more compounds listed or exemplified in any of the following publications: US 2016/0339019 A1 (Laberge et al.); US 20170266211 A1 (David et al.); US 2017/0216286 A1 (Kirkland et al.); US 2017/0281649 A1 (David); Furhmann-Stroissnigg et al. (Nat Commun. 2017 Sep. 4; 8 (1):422), and Blagosklonny (Cancer Biol Ther. 2013 December; 14 (12):1092-7). The aforesaid publications are hereby incorporated herein in their entirety for the purpose of excluding such compounds.
US 2016/0339019 A1 (Laberge et al.) and US 20170266211 A1 (David et al.) are hereby incorporated herein by reference in their entirety for all purposes, including but not limited to the identification, Formulation, and use of compounds for eliminating or reducing the activity of senescent cells and treating particular senescence-related conditions, including but not limited to those referred to in this disclosure. U.S. patent applications US 2018/0000816 A1 and PCT/US2018/046553 are hereby incorporated herein for all purposes, including but not limited to the identification, Formulation, and use of compounds for eliminating or reducing the activity of senescent cells and treating various ophthalmic conditions. U.S. patent applications US 2018/0000816 A1 and PCT/US2018/046567 are hereby incorporated herein for all purposes, including but not limited to the identification, Formulation, and use of compounds for eliminating or reducing the activity of senescent cells and treating various pulmonary conditions. U.S. patent application ser. No. 16/181,163 are hereby incorporated herein for all purposes, including but not limited to the identification, Formulation, and use of compounds for eliminating or reducing the activity of senescent cells and treating atherosclerosis.
This example provides assays by which the reader may ascertain whether a test compound has sufficient inhibitory capacity for the target pathways to be developed as a senolytic agent. Information from these assays may be combined with information from cell lysis assays (Examples 2 and 3) to select compounds for further development.
Inhibition of HSP90a/b is measured using a competitive fluorescence polarization binding assay. Briefly, compounds' ability to inhibit HSP90 ATP hydrolysis affinity is measured through the displacement of a fluorescently labeled geldanamycin from the ATP binding pocket of the protein. As the test compound is titrated in, there is a decrease in the fluorescent intensity parallel to the polarized excitation. The method is based on a that published by Kim et. al. (2004): Development of a fluorescence polarization assay for the molecular chaperone Hsp90. 2004. J. Biomolecular Screening 9 (5): 375-381.
Reactions are performed in 50 μL final volume in black 384-well plates. Each reaction contained 5 nM of FITC-labeled geldanamycin and 30 nM HSP90a or HSP90b in a solution of 20 mM HEPES (pH 7.3), 50 mM KCl, 5 mM MgCl2, 20 mM Na2MoO4, 0.1 mg/mL bovine gamma globulin and 2 mM DTT. Compounds are diluted from DMSO 1:3 dilution series so that when added to the reaction in 2 μL, yield no more than 2% DMSO in the final reaction. Once the compound is added, plates are sealed and reactions allowed to equilibrate for 5 hr. Following equilibration, the fluorescence is measured using a combination of excitation and emission of 488 and 535 nm respectively.
Fluorescence polarization is expressed in millipolarization (mP) units. This is calculated using the following equation: mP=1000×[(Is−ISB)−(Ip−IpB)]/[(Is−ISB)+(Ip−IpB)] where Is and Ip are the parallel and perpendicular emission intensity of the sample and IpB and ISB are the emission intensity of sample lacking HSP90. Percent inhibition was calculated from the following Formula:
% inhibition=100−(mPc−mPb)/(mPg−mPb)×100.
Inhibition of PI3K lipid kinases is measured using a radiometric assay monitoring the enzymatic transfer of phosphate from [γ-32P] ATP to the appropriate lipid substrate. The development of the assay is described by Knight et. al. (2007), and makes use of the fact that lipids, but not ATP will bind to nitrocellulose membrane allowing the quantitation of the PI3K enzymatic activity after removal of the labeled substrate. Knight et al. A membrane capture assay for lipid kinase activity. 2007. Nature Protocols 2 (10): 2459-2466.
Reactions are performed in 96-well plate format. Test compounds are prepared in a 1:3 dilution series at 5× final concentration in 10% DMSO. The kinase of interest is diluted to 1 μg/mL is a solution of 62.5 mM HEPES pH 7.4, 0.25 mg/mL phosphatidylinositol, 25 mM MgCl2, and 2.5 mg/mL bovine serum albumin. Five microliters of inhibitor solution are added per well followed by 10 microliters of the diluted enzyme. The phosphotransfer reaction is initiated by adding 5 microliters solution of 25 μM unlabeled ATP and 0.1-0.25 μCi/μL [γ-32P] ATP. After 20 minutes incubation at room temperature, four microliters of the reaction are spotted onto the nitrocellulose membrane. The membrane is washed five times with solution of 1 M NaCl and 1% phosphoric acid, then dried.
The relative abundance of phosphorylated lipid in each spot, and thereby the residual enzymatic activity of each reaction relative to DMSO control is determined using a phosphor imager. The dried membrane is wrapped in plastic wrap, then exposed to a phosphor screen for 20 minutes. The relative spot intensity of each reaction is measured by scanning the exposed plate on a phosphorimager and quantitated with the associated software analysis package.
Test compounds are assayed for inhibition of the chymotrypsin-like activity of the proteasome β5 subunit by monitoring the release of a fluorogenic product after cleavage of a substrate peptide. The active protease cleaves an amide bond between the C-terminal amino acid of a substrate peptide and aminoemethylcoumarin, allowing enzyme activity to be quantitated fluorometrically.
Compounds are tested in a 384-well format. A 1:3 dilution series of compound in DMSO is diluted into reaction buffer (20 mM HEPES pH 7.5, 0.01% BSA, 0.02% SDS, 0.5 mM EDTA, 100 mM NaCl) so that when added to the reaction mix the final concentration of DMSO does not exceed 1%. To initialize the reaction, test compounds and substrate are added for a final reaction volume of 50 μL per well containing the following: 20 mM HEPES pH 7.5, 0.01% BSA, 0.02% SDS, 0.5 mM EDTA, 100 mM NaCl, 0.5 nM constitutive 20S proteasome, and 50 μM substrate (Succinyl-Leu-Leu-Val-Tyr-AMC).
Reactions are mixed and an initial reading is recorded after 5 minutes using and excitation wavelength of 360 nM and emission of 450 nM. A second, endpoint measurement is taken at 1 hour. Relative enzymatic activity is calculated from the change in fluorescence (final minus initial) relative to DMSO control.
Inhibition of HDACs by test compounds is assessed by monitoring the electrophoretic shift in fluorescently labeled substrate peptides resulting from enzymatic activity. Deacetylation results in a change in the overall charge of substrate peptides and thus effects its migration in an electric field, thus resolving the fluorescently labeled reaction substrate and product.
Test compounds are diluted 1:3 in DMSO then added to solution of 100 mM HEPES pH 7.4, 0.1% BSA, 0.01% Triton X-100, 30 mM KCl, and 2 μM substrate peptide (FITC-AHA-TSPQPKK-Ac-NH2). Ten μL of this mix is added wells of a 384-well plate containing 10 μL of the same buffer containing the HDAC protein in place of the substrate (5 nM HDAC1, 5 nM HDAC2, 0.5 nM HDAC3 or 3 nM HDAC8). The reaction is incubated at 25° C. for 3 hours, then terminated by adding 1.22× stop buffer.
The enzymatic activity and percent inhibition is determined using a Caliper LabChip™ 3000 Drug Discovery System (Perkin Elmer). Plates are loaded with the terminated reaction and spatially resolved fluorescence of the reaction substrates and products are quantitated.
The enzymatic activity in each individual reaction is calculated as the product sum ratio (PSR) using the following equation: PSR=(P/(S+P) where P is the peak height of the product species and S is the peak height of the substrate. The percent inhibition (PI) for each reaction is then calculated with the following equation: PI=(PSRNNI−PSRC)/(PSRNI−PSRNE)*100 where PSRNI is the PSR with no compound, PSRC is the PSR of the reaction in question, and PSRNE is the PSR of a reaction containing no enzyme. PI values were used to create dose response curves and calculated IC50 values for test compounds.
Inhibition of p97 by candidate molecules can be assessed by measuring NADH consumption in an enzyme-linked assay of p97 ATPase activity. The assay includes pyruvate kinase and lactate dehydrogenase to consume a molecule of NADH in a non-rate limiting manner for each molecule of ATP hydrolyzed by p97. NADH consumption is followed by monitoring the decrease in absorbance at 340 nm as NADH is converted to NAD+.
To conduct the assay, a 1:3 serial dilution of a compound in DMSO is added to 50 μL reactions in a 384-well plate containing 60 nM p97, 3 units/mL of pyruvate kinase and lactate-dehydrogenase with 500 μM ATP, 250 μM NADH, and 3.75 mM phosphoenolpyruvate. IC50 values are calculated using end-point measurements; after two hours of incubation, the absorbance at 340 nM is measured and values are plotted relative to DMSO control. The ATP competitive nature of candidate compounds is assessed using similar assay conditions, but varying the concentration of ATP.
Before initiating experiments in vivo, it is usually helpful to screen potential senolytic agents for their potency for removing senescent cells, and their selectivity for senescent cells in comparison with non-senescent cells in the same tissue.
Human fibroblast IMR90 cells can be obtained from the American Type Culture Collection (ATCC®) with the designation CCL-186. The cells are maintained at <75% confluency in DMEM containing FBS and Pen/Strep in an atmosphere of 3% O2, 10% CO2, and ˜95% humidity. The cells are divided into three groups: irradiated cells (cultured for 14 days after irradiation prior to use), proliferating normal cells (cultured at low density for one day prior to use), and quiescent cells (cultured at high density for four day prior to use).
On day 0, the irradiated cells are prepared as follows. IMR90 cells are washed, placed in T175 flasks at a density of 50,000 cells per mL, and irradiated at 10-15 Gy. Following irradiation, the cells are plated at 100 μL in 96-well plates. On days 1, 3, 6, 10, and 13, the medium in each well is aspirated and replaced with fresh medium.
On day 10, the quiescent healthy cells are prepared as follows. IMR90 cells are washed, combined with 3 mL of TrypLE trypsin-containing reagent (Thermofisher Scientific, Waltham, Mass.) and cultured for 5 min until the cells have rounded up and begin to detach from the plate. Cells are dispersed, counted, and prepared in medium at a concentration of 50,000 cells per mL. 100 μL of the cells is plated in each well of a 96-well plate. Medium is changed on day 13.
On day 13, the proliferating healthy cell population is prepared as follows. Healthy IMR90 cells are washed, combined with 3 mL of TrypLE and cultured for 5 minutes until the cells have rounded up and begin to detach from the plate. Cells are dispersed, counted, and prepared in medium at a concentration of 25,000 cells per mL. 100 μL of the cells is plated in each well of a 96-well plate.
On day 14, test inhibitors are combined with the cells as follows. A DMSO dilution series of each test compound is prepared at 200 times the final desired concentration in a 96-well PCR plate. Immediately before use, the DMSO stocks are diluted 1:200 into pre-warmed complete medium. Medium is aspirated from the cells in each well, and 100 μL/well of the compound containing medium is added.
Candidate senolytic agents for testing are cultured with the cells for 6 days, replacing the culture medium with fresh medium and the same compound concentration on day 17. Test inhibitors are cultured with the cells for 3 days. The assay system uses the properties of a thermostable luciferase to enable reaction conditions that generate a stable luminescent signal while simultaneously inhibiting endogenous ATPase released during cell lysis. At the end of the culture period, 100 μL of CellTiter-Glo® reagent (Promega Corp., Madison, Wis.) is added to each of the wells. The cell plates are placed for 30 seconds on an orbital shaker, and luminescence is measured.
Human umbilical vein (HUVEC) cells from a single lot were expanded in Vascular Cell Basal Media supplemented with the Endothelial Cell Growth Kit™-VEGF from ATCC to approximately eight population doublings then cryopreserved. Nine days prior to the start of the assay, cells for the senescent population were thawed and seeded at approximately 27,000/cm2. All cells were cultured in humidified incubators with 5% CO2 and 3% O2 and media was changed every 48 hr. Two days after seeding, the cells were irradiated, delivering 12 Gy radiation from an X-ray source. Three days prior to the start of the assay, cells for the non-senescent populations are thawed and seeded as for the senescent population. One day prior to the assay, all cells were trypsinized and seeded into 384-well plates, 5,000/well senescent cells and 10,000/well non-senescent in separate plates in a final volume of 55 μL/well. In each plate, the central 308 wells contained cells and the outer perimeter of wells was filled with 70 μL/well deionized water.
On the day of the assay, compounds were diluted from 10 mM stocks into media to provide the highest concentration working stock, aliquots of which were then further diluted in media to provide the remaining two working stocks. To initiate the assay, 5 μL of the working stock was added to the cell plates. The final test concentrations were 20, 2, and 0.2 μM. In each plate, 100 test compounds were assayed in triplicate at a single concentration along with a three wells of a positive control and five no treatment (DMSO) controls. Following compound addition, the plates are returned to the incubators for three days.
Cell survival was assessed indirectly by measuring total ATP concentration using CellTiter-Glo™ reagent (Promega). The resultant luminescence was quantitated with an EnSpire™ plate reader (Perkin Elmer). The relative cell viability for each concentration of a compound was calculated as a percentage relative to the no-treatment controls for the same plate.
For follow-up dose responses of potential lead compounds, 384-well plates of senescent and non-senescent cells were prepared as described above. Compounds were prepared as 10-point 1:3 dilution series in DMSO, then diluted to 12× in media. Five microliters of this working stock was then added to the cell plates. After three days of incubation, cell survival relative to DMSO control was calculated as described above. All measurements were preformed in quadruplicate.
This example illustrates the testing of an MDM2 inhibitor in a mouse model for treatment of osteoarthritis. It can be adapted mutatis mutandis to test and develop senolytic agents for use in clinical therapy.
The model was implemented as follows. C57BL/6J mice underwent surgery to cut the anterior cruciate ligament of one rear limb to induce osteoarthritis in the joint of that limb. During week 3 and week 4 post-surgery, the mice were treated with 5.8 μg of Nutlin-3A (n=7) per operated knee by intra-articular injection, q.o.d. for 2 weeks. At the end of 4 weeks post-surgery, joints of the mice were monitored for presence of senescent cells, assessed for function, monitored for markers of inflammation, and underwent histological assessment.
Two control groups of mice were included in the studies performed: one group comprising C57BL/6J or 3MR mice that had undergone a sham surgery (n=3) (i.e., surgical procedures followed except for cutting the ACL) and intra-articular injections of vehicle parallel to the GCV (gancyclovir) treated group; and one group comprising C57BL/6J or 3MR mice that had undergone an ACL surgery and received intra-articular injections of vehicle (n=5) parallel to the GCV-treated group. RNA from the operated joints of mice from the Nutlin-3A treated mice was analyzed for expression of SASP factors (mmp3, IL-6) and senescence markers (p16). qRT-PCR was performed to detect mRNA levels.
Function of the limbs was assessed 4 weeks post-surgery by a weight bearing test to determine which leg the mice favored. The mice were allowed to acclimate to the chamber on at least three occasions prior to taking measurements. Mice were maneuvered inside the chamber to stand with one hind paw on each scale. The weight that was placed on each hind limb was measured over a three second period. At least three separate measurements were made for each animal at each time point. The results were expressed as the percentage of the weight placed on the operated limb versus the contralateral unoperated limb.
This example illustrates the testing of a Bcl inhibitor in a mouse model for treatment of a back-of-the eye disease, specifically diabetic retinopathy. It can be adapted mutatis mutandis to test senolytic agents for use in clinical therapy.
The efficacy of model compound UBX1967 (a Bcl-xL inhibitor) was studied in the mouse oxygen-induced retinopathy (OIR) model (Scott and Fruttiger, Eye (2010) 24, 416-421, Oubaha et al, 2016). C57B1/6 mouse pups and their CD1 foster mothers were exposed to a high oxygen environment (75% O2) from postnatal day 7 (P7) to P12. At P12, animals were injected intravitreally with 1 μl test compound (200, 20, or 2 uM) Formulated in 1% DMSO, 10% Tween-80, 20% PEG-400, and returned to room air until P17. Eyes were enucleated at P17 and retinas dissected for either vascular staining or qRT-PCR. To determine avascular or neovascular area, retinas were flat-mounted, and stained with isolectin B4 (IB4) diluted 1:100 in 1 mM CaCl2. For quantitative measurement of senescence markers (e.g., Cdkn2a, Cdkn1a, Il6, Vegfa), qPCR was performed. RNA was isolated and cDNA was generated by reverse-transcription, which was used for qRT-PCR of the selected transcripts.
The efficacy of UBX1967 was also studied in the streptozotocin (STZ) model. C57BL/6J mice of 6- to 7-week were weighted and their baseline glycemia was measured (Accu-Chek™, Roche). Mice were injected intraperitoneally with STZ (Sigma-Alderich, St. Louis, Mo.) for 5 consecutive days at 55 mg/Kg. Age-matched controls were injected with buffer only. Glycemia was measured again a week after the last STZ injection and mice were considered diabetic if their non-fasted glycemia was higher than 17 mM (300 mg/L). STZ treated diabetic C57BL/6J mice were intravitreally injected with 1 μl of UBX1967 (2 μM or 20 μM, Formulated as a suspension in 0.015% polysorbate-80, 0.2% Sodium Phosphate, 0.75% Sodium Chloride, pH 7.2) at 8 and 9 weeks after STZ administration. Retinal Evans blue permeation assay was performed at 10 weeks after STZ treatment.
This example illustrates the testing of inhibitors in a mouse model for treatment of lung disease: specifically, a model for idiopathic pulmonary fibrosis (IPF). It can be adapted mutatis mutandis to test and develop senolytic agents for use in clinical therapy.
As a model for chronic obstructive pulmonary disease (COPD), mice were exposed to cigarette smoke. The effect of a senolytic agent on the mice exposed to smoke is assessed by senescent cell clearance, lung function, and histopathology.
The mice used in this study include the 3MR strain, described in US 2017/0027139 A1 and in Demaria et al., Dev Cell. 2014 Dec. 22; 31 (6): 722-733. The 3MR mouse has a transgene encoding thymidine kinase that converts the prodrug gancyclovir (GCV) to a compound that is lethal to cells. The enzyme in the transgene is placed under control of the p16 promoter, which causes it to be specifically expressed in senescent cells. Treatment of the mice with GCV eliminates senescent cells.
Other mice used in this study include the INK-ATTAC strain, described in US 2015/0296755 A1 and in Baker et al., Nature 2011 Nov. 2; 479 (7372):232-236. The INK-ATTAC mouse has a transgene encoding switchable caspase 8 under control of the p16 promoter. The caspase 8 can be activated by treating the mice with the switch compound AP20187, whereupon the caspase 8 directly induces apoptosis in senescent cells, eliminating them from the mouse.
To conduct the experiment, six-week-old 3MR (n=35) or INK-ATTAC (n=35) mice were chronically exposed to cigarette smoke generated from a Teague TE-10 system, an automatically-controlled cigarette smoking machine that produces a combination of side-stream and mainstream cigarette smoke in a chamber, which is transported to a collecting and mixing chamber where varying amounts of air is mixed with the smoke mixture. The COPD protocol was adapted from the COPD core facility at Johns Hopkins University (Rangasamy et al., 2004, J. Clin. Invest. 114:1248-1259; Yao et al., 2012, J. Clin. Invest. 122:2032-2045).
Mice received a total of 6 hours of cigarette smoke exposure per day, 5 days a week for 6 months. Each lighted cigarette (3R4F research cigarettes containing 10.9 mg of total particulate matter (TPM), 9.4 mg of tar, and 0.726 mg of nicotine, and 11.9 mg carbon monoxide per cigarette [University of Kentucky, Lexington, Ky.]) was puffed for 2 seconds and once every minute for a total of 8 puffs, with the flow rate of 1.05 L/min, to provide a standard puff of 35 cm3. The smoke machine was adjusted to produce a mixture of side stream smoke (89%) and mainstream smoke (11%) by smoldering 2 cigarettes at one time. The smoke chamber atmosphere was monitored for total suspended particulates (80-120 mg/m3) and carbon monoxide (350 ppm).
Beginning at day 7, (10) INK-ATTAC and (10) 3MR mice were treated with AP20187 (3× per week) or gancyclovir (5 consecutive days of treatment followed by 16 days off drug, repeated until the end of the experiment), respectively. An equal number of mice received the corresponding vehicle. The remaining 30 mice (15 INK-ATTAC and 15 3MR) were evenly split with 5 of each genetically modified strain placed into three different treatment groups. One group (n=10) received Nutlin-3A (25 mg/kg dissolved in 10% DMSO/3% Tween-20™ in PBS, treated 14 days consecutively followed by 14 days off drug, repeated until the end of the experiment). One group (n=10) received ABT-263 (Navitoclax) (100 mg/kg dissolved in 15% DMSO/5% Tween-20, treated 7 days consecutively followed by 14 days off drug, repeated until the end of the experiment), and the last group (n=10) received only the vehicle used for ABT-263 (15% DMSO/5% Tween-20), following the same treatment regimen as ABT-263. An additional 70 animals that did not receive exposure to cigarette smoke were used as controls for the experiment.
After two months of cigarette smoke (CS) exposure, lung function was assessed by monitoring oxygen saturation using the MouseSTAT PhysioSuite™ pulse oximeter (Kent Scientific). Animals were anesthetized with isoflurane (1.5%) and the toe clip was applied. Mice were monitored for 30 seconds and the average peripheral capillary oxygen saturation (SpO2) measurement over this duration was calculated.
This example illustrates the testing of an MDM2 inhibitor in a mouse model for treatment of atherosclerosis. The test compounds are administered systemically rather than locally. The model is done in an LDLR−/− strain of mice, which are deficient in the receptor for low-density lipoprotein. The experiments described here can be adapted mutatis mutandis to test and develop other types of inhibitors for use in clinical therapy.
Two groups of LDLR−/− mice (10 weeks) are fed a high fat diet (HFD) (Harlan Teklad TD.88137) having 42% calories from fat, beginning at Week 0 and throughout the study. Two groups of LDLR−/− mice (10 weeks) are fed normal chow (−HFD). From weeks 0-2, one group of HFD mice and −HFD mice are treated with Nutlin-3A (25 mg/kg, intraperitoneally). One treatment cycle is 14 days treatment, 14 days off. Vehicle is administered to one group of HFD mice and one group of −HFD mice. At week 4 (timepoint 1), one group of mice are sacrificed and to assess presence of senescent cells in the plaques. For the some of the remaining mice, Nutlin-3A and vehicle administration is repeated from weeks 4-6. At week 8 (timepoint 2), the mice are sacrificed and to assess presence of senescent cells in the plaques. The remaining mice are treated with Nutlin-3A or vehicle from weeks 8-10. At week 12 (timepoint 3), the mice are sacrificed and to assess the level of plaque and the number of senescent cells in the plaques.
Plasma lipid levels were measured in LDLR−/− mice fed a HFD and treated with Nutlin-3A or vehicle at timepoint 1 as compared with mice fed a −HFD (n=3 per group). Plasma was collected mid-afternoon and analyzed for circulating lipids and lipoproteins.
At the end of timepoint 1, LDLR−/− mice fed a HFD and treated with Nutlin-3A or vehicle were sacrificed (n=3, all groups), and the aortic arches were dissected for RT-PCR analysis of SASP factors and senescent cell markers. Values were normalized to GAPDH and expressed as fold-change versus age-matched, vehicle-treated LDLR−/− mice on a normal diet. The data show that clearance of senescent cells with Nutlin-3A in LDLR−/− mice fed a HFD reduced expression of several SASP factors and senescent cell markers, MMP3, MMP13, PAI1, p21, IGFBP2, IL-1A, and IL-1B after one treatment cycle.
At the end of timepoint 2, LDLR−/− mice fed a HFD and treated with Nutlin-3A or vehicle (n=3 for all groups) were sacrificed, and aortic arches were dissected for RT-PCR analysis of SASP factors and senescent cell markers. Values were normalized to GAPDH and expressed as fold-change versus age-matched, vehicle-treated LDLR−/− mice on a normal diet. The data show expression of some SASP factors and senescent cell markers in the aortic arch within HFD mice. Clearance of senescent cells with multiple treatment cycles of Nutlin-3A in LDLR−/− mice fed a HFD reduced expression of most markers.
At the end of timepoint 3, LDLR−/− mice fed a HFD and treated with Nutlin-3A or vehicle (n=3 for all groups) were sacrificed, and aortas were dissected and stained with Sudan IV to detect the presence of lipid. Body composition of the mice was analyzed by MRI, and circulating blood cells were counted by Hemavet™.
New p97 inhibitors according to this invention may be developed not only for treating conditions mediated by senescent cells, but also conditions mediated by cancer cells.
The ability of compounds to specifically kill cancer cells can be tested in assays using other established cell lines. These include HeLa cells, OVCAR-3, LNCaP, and any of the Authenticated Cancer Cell Lines available from Millipore Sigma, Burlington Mass., U.S.A. Compounds specifically kill cancer cells if they are lethal to the cells at a concentration that is at least 5-fold lower, and preferably 25- or 100-fold lower than a non-cancerous cell of the same tissue type. The control cell has morphologic features and cell surface markers similar to the cancer cell line being tested, but without signs of cancer.
In vivo, compounds are evaluated in flank xenograft models established from sensitive SCLC (H889) and hematologic (RS4; 11) cell lines, or using other tumor-forming cancer cell lines, according to what type of cancer is of particular interest to the user. When dosed orally or intravenously, compounds induce rapid and complete tumor responses (CR) that are durable for several weeks after the end of treatment in all animals bearing H889 (SCLC) or RS4; 11 (ALL) tumors. Similar treatment of mice bearing H146 SCLC tumors can induce rapid regressions in the animals.
The several hypotheses presented in this disclosure provide a premise by way of which the reader may understand the invention. This premise is provided for the intellectual enrichment of the reader. Practice of the invention does not require detailed understanding or application of the hypothesis. Except where stated otherwise, features of the hypothesis presented in this disclosure do not limit application or practice of the claimed invention.
For example, except where the elimination of senescent cells is explicitly required, the compounds of this invention may be used for treating the conditions described regardless of their effect on senescent cells. Although many of the senescence-related conditions referred to in this disclosure occur predominantly in older patients, the occurrence of senescent cells and the pathophysiology they mediate can result from other events, such as irradiation, other types of tissue damage, other types of disease, genetic abnormalities, and invention. The invention may be practiced on patients of any age having the condition indicated, unless otherwise explicitly indicated or required.
Although the compounds and compositions referred to in this disclosure are illustrated in the context of eliminating senescent cells and treating senescence-associated conditions, compounds and their derivatives that are novel can be prepared according to this invention for any purpose, including but not limited to laboratory use, the treatment of senescence-related conditions, the poisoning of in-laws, and the treatment of other conditions such as cancer.
While the invention has been described with reference to the specific examples and illustrations, changes can be made and equivalents can be substituted to adapt to a particular context or intended use as a matter of routine development and optimization and within the purview of one of ordinary skill in the art, thereby achieving benefits of the invention without departing from the scope of what is claimed and their equivalents.
This application claims the priority benefit of U.S. provisional patent applications 62/612,411, 62/612,414, 62/612,416, 62/612,417, and 62/612,418, all filed Dec. 30, 2017, and 62/676,692, filed May 25, 2018. The aforelisted applications are hereby incorporated herein by reference in their entirety for all purposes.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2018/068003 | 12/28/2018 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62612411 | Dec 2017 | US | |
| 62612414 | Dec 2017 | US | |
| 62612416 | Dec 2017 | US | |
| 62612417 | Dec 2017 | US | |
| 62612418 | Dec 2017 | US | |
| 62676692 | May 2018 | US |
