Patent Application
20200231941
Pursuant to the EFS-Web legal framework and 37 C.F.R. §§ 1.821-825), a Sequence Listing in the form of an ASCII-compliant text file (entitled “7055PAT193-SequenceListing_ST25.txt” created on Mar. 5, 2020 having a size of 6,347 bytes) is submitted herewith the instant application, and the entire contents of the Sequence Listing are incorporated herein by reference.
The present invention relates to a gene-modified coxsackievirus and a pharmaceutical composition applicable to cancer treatment. The present invention is useful in the field of oncolytic virotherapy.
Oncolytic virotherapy is a treatment method in which cancer cells are infected with a virus and, while allowing the virus to proliferate inside the cancer tissue, an oncolytic property that the virus has are used to destroy or kill the cancer tissue. Clinical research using an adenovirus or a herpes simplex virus, either of which is a DNA virus, has been performed on brain tumor or breast cancer as a target and results indicating safety and effectiveness are being reported.
Coxsackievirus group B type 3 (CVB3) (Non-Patent Literatures 1 to 3) has a positive sense single-stranded RNA genome, proliferates only within cytoplasm, is low in possibility of insertional mutagenesis of a host cell genome, and is thus considered to be comparatively high in safety for oncolytic virotherapy. Also, CVB3 is a commonplace virus and in many cases, even when infection occurs, it is limited to asymptomatic infection. However, there are reports concerning relevance to aseptic meningitis, viral myocarditis, and pancreatitis. Also, in regard to CVB3, a significant oncolytic property against human non-small cell lung cancer has been reported (Non-Patent Literature 4).
On the other hand, coxsackievirus A21 (CVA21) is known as a virus for which application to oncolytic virotherapy is anticipated (Patent Literature 1), and it has been reported that the virus has been proliferated tissue-specifically by incorporating miRNA in the virus genome (Non-Patent Literature 5).
According to studies thus far by the present inventors, in in vivo evaluation of wild-type CVB3 (CVB-WT), occurrences of increases in AMY, CK, AST, and ALT were observed in serum biochemical examination and destruction of exocrine tissue in the pancreas, inflammatory dampening in myocardium, and inflammatory dampening in the liver were observed in histological diagnosis. These undesirable actions are preferably mitigated.
Also, from a standpoint of securing safety in use of oncolytic virotherapy, it is strongly desired, regardless of presence/non-presence of undesirable actions, that virus proliferation in normal cells other than targeted cancer cells be suppressed to further improve safety.
An object of the present invention is to provide a gene-modified coxsackievirus and a pharmaceutical composition that are applicable in the field of oncolytic virotherapy of treating cancers and are excellent in antitumor effects and safety.
The present inventors attempted insertion of a target sequence for tissue-specific microRNA (miRNA) into the genome 5′ untranslated region (UTR) and/or the genome 3′ UTR of CVB3-WT. It was anticipated that thereby, in tissue in which the miRNA is present, a RISC complex that contains the miRNA would bind to the inserted target sequence to inhibit virus protein translation and thereby suppress virus proliferation tissue-specifically.
In this process, the present inventors made note of the miR-34 family that so far has not been studied whatsoever for use in similar purposes.
This miR-34 family is positioned downstream a p53 gene, which is a type of tumor suppressor gene, and has been reported to be involved in cell cycle, apoptosis, cell senescence, and so forth in cells all over the body (see
The present inventors made note of the abovementioned high expression of the miR-34 family in normal cells and the deletion and reduction of expression in cancer cells and attempted to prepare, by inserting a target sequence for miR-34 in the CVB3-WT genome, a gene-modified coxsackievirus of excellent safety with which virus proliferation can be suppressed in non-cancerated normal cells and the virus can proliferate efficiently in cancer cells to exhibit an oncolytic property.
Further, the present inventors also studied use of tissue-specifically expressed miRNAs to reduce actions caused by CVB-WT. One is miR-217 that is said to be expressed specifically in the pancreas and another is miR-1 that is said to be expressed specifically in muscle tissue and normal cells.
Also, in studying insertion of a target sequence for a specific miRNA into a genome, it was determined that even in the 3′ UTR, virus replication is hindered depending on the insertion position, and a finding that an appropriate insertion position must be found was thereby obtained. An optimal position was thus determined for the position of insertion of the target sequence for the miRNA into the genome. Also, a position of insertion of a target sequence for a specific miRNA into the genome in the 5′ UTR was studied to determine an insertion position of the target sequence with which gene replication is not hindered.
Further, a study was performed upon noting that by using the 5′ UTR as the position of insertion of the target sequence for the specific miRNA into the genome, there is a possibility that detachment of the inserted target sequence from the virus genome becomes unlikely.
To achieve the above object, a gene-modified coxsackievirus of the present invention contains a mutated genome with a coxsackievirus wild-type (CVB3-WT) genome inserted with at least one polynucleotide constituted of a target sequence for a normal-cell-specific or tissue-specific microRNA (miRNA) and has an arrangement with which proliferation is suppressed specifically in normal cells and the target sequence for the normal-cell-specific miRNA corresponds to at least one of miR-34a and miR-34c.
Here, by containing the mutated genome with the coxsackievirus wild-type (CVB3-WT) genome inserted with at least one polynucleotide constituted of the target sequence for the normal-cell-specific or tissue-specific microRNA (miRNA), virus proliferation can be suppressed in tissue in which the miRNA is present. That is, a RISC complex that contains the miRNA binds to the inserted target sequence to inhibit virus protein translation and virus proliferation can thus be suppressed tissue-specifically.
Also, by the target sequence for the normal-cell-specific miRNA corresponding to at least one of miR-34a and miR-34c, virus proliferation can be suppressed in tissue in which miR-34a or miR-34c is present. That is, the miR-34 family that includes miR-34a and miR-34c is expressed highly in normal cells and therefore virus proliferation in normal cells can be suppressed to improve safety. Also, in tissue in which miR-34a or miR-34c is not present, that is, in cancer cells in which deletion or reduction of expression of the miR-34 family is seen, the virus can proliferate to enable antitumor effects to be exhibited selectively.
Also, if a position at which the polynucleotide is inserted is at least one of either of inside the 5′ UTR region and inside the 3′ UTR region of the CVB3-WT genome, replication is unlikely to be hindered during virus replication within host cells. That is, the 5′ UTR region or the 3′ UTR region is an untranslated region that is not translated into a protein, and therefore the insertion of the target sequence into the CVB3-WT genome is unlikely to affect virus RNA translation in the host cells and the virus RNA translation would be performed appropriately. Accordingly, protein synthesis and virus particle replication proceed and the virus can proliferate to enable the antitumor effects to be exhibited on the cancer cells.
Also, if the position at which the polynucleotide is inserted is between positions 7304 and 7305 inside the 3′ UTR region of the CVB3-WT genome, replication is more unlikely to be hindered during the virus replication within the host cells.
The position between the positions 7304 and 7305 is inside the 3′ UTR region of the CVB3-WT genome and is shifted by four bases downstream from a base sequence constituting a termination codon that terminates translation of the CVB3-WT genome into proteins (positions 7298, 7299, and 7300 constitute the termination codon). That is, due to being a position inside the 3′ UTR region and close to the termination codon, translation can be ended appropriately while retaining a three-dimensional structure of the 3′ UTR necessary for replication. Consequently, the virus can proliferate in the cancer cells and destroy the cancer cells more stably.
Also, if the position at which the polynucleotide is inserted is between positions 742 and 743 inside the 5′ UTR region of the CVB3-WT genome, replication is more unlikely to be hindered during the virus replication within the host cells. Also, the state in which the polynucleotide is inserted in the CVB3-WT genome is maintained more readily and the polynucleotide can be made more unlikely to be removed from the genome.
The position between the positions 742 and 743 is inside the 5′ UTR region of the CVB3-WT genome and corresponds to being immediately upstream a base sequence constituting an initiation codon that initiates the translation of the CVB3-WT genome into proteins (positions 743, 744, and 745 constitute the initiation codon). That is, due to being a position inside the 5′ UTR region and adjacent the initiation codon, translation can be ended appropriately while retaining a three-dimensional structure of the 5′ UTR necessary for replication. Also, the polynucleotide inserted in the 5′ UTR region was less likely to become detached from the genome than the polynucleotide inserted in the 3′ UTR region. Consequently, the virus can be hindered from proliferating in normal cells and the virus can efficiently proliferate in the cancer cells and destroy the cancer cells more stably.
Also, if a plurality of the polynucleotides constituted of the target sequence are inserted, a probability, in tissue in which the miRNA is present, of a RISC complex containing the miRNA binding to the target sequence can be increased to enable deviation from the miRNA to be avoided even when further virus genome mutation occurs, and the tissue-specific virus proliferation suppression can thus be further ensured.
Also, if the inserted polynucleotide is (a) or (b) shown below or a polynucleotide constituted of a sequence with which one to several nucleotides are deleted, substituted, or added with respect to (a) or (b), it would be that with which four target sequences for miR-34a or miR-34c are aligned with spacer sequences in between. The proliferation of the virus can thereby be suppressed more reliably in tissue in which miR-34a or miR-34c is present. Also, in tissue in which miR-34a or miR-34c is not present, that is, in the cancer cell, the virus can proliferate to enable the antitumor effects to be exhibited selectively. Here, the region in which the polynucleotide is inserted includes an arrangement constituted of just the inside of the 5′ UTR region of the CVB3-WT genome, an arrangement constituted of just the inside of the 3′ UTR region of the CVB3-WT genome, and an arrangement constituted of both the inside of the 5′ UTR region and the inside of the 3′ UTR region of the CVB3-WT genome.
Also, if the polynucleotide is inserted in each of the inside of the 5′ UTR region and the inside of the 3′ UTR region of the CVB3-WT genome, this would mean that the inserted number of target sequences for miR-34a or miR-34c is increased and the proliferation of the virus can be suppressed even more reliably in tissue in which miR-34a or miR-34c is present. Also, even if the inserted polynucleotide becomes detached from the genome in one of the regions inside the 5′ UTR region or inside the 3′ UTR region, by the polynucleotide inserted in the other region being present, the proliferation of the virus can be suppressed stably in tissue in which miR-34a or miR-34c is present.
Also, if the tissue-specific miRNA includes at least one of miR-1 and miR-217, the proliferation of the gene-modified coxsackievirus can be suppressed tissue-specifically in the pancreas, the liver, or muscle tissue. That is, undesirable actions that occur when CVB3-WT is introduced into cells of the pancreas, the liver, or muscle tissue can be reduced or deterred.
Also, if the polynucleotide is (c) or (d) shown below or is a polynucleotide constituted of a sequence with which one to several nucleotides are deleted, substituted, or added with respect to (c) or (d), a polynucleotide constituted of two target sequences for miR-34a and two target sequences for miR-217 or a polynucleotide constituted of two target sequences for miR-34c and two target sequences for miR-217 is inserted in the CVB3-WT genome as the sequences targeted by miRNA. The proliferation of the virus can thereby be suppressed not just in tissue in which miR-34a or miR-34c is present but also in tissue in which miR-217 is present. Consequently, the safety in using the gene-modified coxsackievirus can be increased further. In particular, when CVB3-WT is used, the pancreas is where undesirable side effects occur strongly, and because high expression of miR-217 in the pancreas is seen, the polynucleotide suppresses the occurrence of side effects in the pancreas to contribute to improvement of safety. In the polynucleotide sequences here, spacer sequences are interposed between individual target sequences. Also, here, the region in which the polynucleotide is inserted includes an arrangement constituted of just the inside of the 5′ UTR region of the CVB3-WT genome, an arrangement constituted of just the inside of the 3′ UTR region of the CVB3-WT genome, and an arrangement constituted of both the inside of the 5′ UTR region and the inside of the 3′ UTR region of the CVB3-WT genome.
Also, if the polynucleotide is inserted in each of the inside of the 5′ UTR region and the inside of the 3′ UTR region of the CVB3-WT genome, this would mean that the numbers of inserted target sequences for miR-34a and miR-217 or for miR-34c and miR-217 are increased and the proliferation of the virus can be suppressed even more reliably in tissue in which miR-34a and miR-217 or miR-34c and miR-217 are present. Also, even if the inserted polynucleotide becomes detached from the genome in one of the regions inside the 5′ UTR region or inside the 3′ UTR region, by the polynucleotide inserted in the other region being present, the proliferation of the virus can be suppressed stably in tissue in which miR-34a and miR-217 or miR-34c and miR-217 are present.
Also, if the polynucleotide is (e) or (f) shown below or a sequence with which one to several nucleotides are deleted, substituted, or added with respect to (e) or (f), a polynucleotide constituted of two target sequences for miR-34a and two target sequences for miR-1 or a polynucleotide constituted of two target sequences for miR-34c and two target sequences for miR-1 is inserted in the CVB3-WT genome as the sequence targeted by miRNA. The proliferation of the virus can thereby be suppressed not just in tissue in which miR-34a or miR-34c is present but also in tissue in which miR-1 is present. Consequently, the safety in using the gene-modified coxsackievirus can be increased further. In the polynucleotide sequences here, spacer sequences are interposed between individual target sequences. Also, here, the region in which the polynucleotide is inserted includes an arrangement constituted of just the inside of the 5′ UTR region of the CVB3-WT genome, an arrangement constituted of just the inside of the 3′ UTR region of the CVB3-WT genome, and an arrangement constituted of both the inside of the 5′ UTR region and the inside of the 3′ UTR region of the CVB3-WT genome.
The gene-modified coxsackievirus according to the present invention is applicable in the field of oncolytic virotherapy of treating cancers and is excellent in antitumor effects and safety.
Also, a pharmaceutical composition according to the present invention is applicable in the field of oncolytic virotherapy of treating cancers and is excellent in antitumor effects and safety.
When, in regard to the present invention, a numerical range is expressed as “X to Y,” the range includes the values X and Y at both ends. When used in regard to the present invention, “A and/or B” means (i) at least one of A and B, or (ii) at least one of A or at least one of B.
[Gene-Modified Coxsackievirus]
One aspect of a gene-modified coxsackievirus provided by the present invention is a gene-modified coxsackievirus that contains a mutated genome with a coxsackievirus wild-type (CVB3-WT) genome inserted with at least one polynucleotide constituted of a target sequence for a tissue-specific microRNA (miRNA). Such a gene-modified coxsackievirus can be tissue-specifically suppressed in proliferation.
A normal-cell-specific miRNA (and its target sequence) used in the present invention is at least one of either of miR-34a and miR-34c. miR-34a or miR-34c is a member of the miR-34 family that has been seen to be highly expressed in normal cells all over the body. Just one of miR-34a and miR-34c may be used or the two may be used in combination.
The miR-34a sequence (SEQ ID NO: 1) and the miR-34c sequence (SEQ ID NO: 2) are shown in
With the present invention, a position at which the target sequence for the normal-cell- or tissue-specific miRNA is inserted is preferably inside a 5′ UTR region or inside a 3′ UTR region of the CVB3-WT genome. Also, the position at which the target sequence for the normal-cell- or tissue-specific miRNA is inserted is more preferably a region in each of inside the 5′ UTR region and inside the 3′ UTR region of the CVB3-WT genome.
Also, if the position at which the target sequence for the tissue-specific miRNA is inserted is inside the 3′ UTR region of the CVB3-WT genome, the position is more preferably more upstream than position 7344 or more downstream than position 7345 of the CVB3-WT genome and is even more preferably between positions 7304 and 7305.
According to studies by the present inventors thus far, gene-modified CVB3 with the target sequence inserted between 7304 and 7305 bp was seen to proliferate in HeLa cells, which are general CVB3-producing cells, proliferation was not seen with gene-modified CVB3 with the target sequence inserted between 7344 and 7345 bp. Also, the same phenomena were seen with HeLa cells in which expression of miRNA was suppressed. Therefore, as stated above, the position at which the target sequence for the tissue-specific miRNA is inserted is preferably inside the 3′ UTR region of the CVB3-WT genome, more preferably more upstream than the position 7344 or more downstream than the position 7345 of the CVB3-WT genome, and even more preferably between the positions 7304 and 7305.
Also, if the position at which the target sequence for the tissue-specific miRNA is inserted is inside the 5′ UTR region of the CVB3-WT genome, the position is preferably between positions 742 and 743 of the CVB3-WT genome.
Also, the number of inserted target sequences for miR-34a or miR-34c is preferably plural, for example, two to six.
In an especially preferable aspect, the inserted polynucleotide is (a) or (b) shown below. Or, it is a polynucleotide constituted of a sequence with which one to several nucleotides are deleted, substituted, or added with respect to (a) or (b) and is capable of functioning in the same manner as (a) or (b), that is, is capable of suppressing proliferation specifically in normal cells when inserted in at least one of between the positions 742 and 743 of the CVB3-WT genome (5′ UTR region), between the positions 7304 and 7305 of the CVB3-WT genome (3′ UTR region), and the respective regions between the positions 742 and 743 of the CVB3-WT genome (5′ UTR region) and between the positions 7304 and 7305 of the CVB3-WT genome (3′ UTR region) to arrange the gene-modified coxsackievirus. Or, the inserted polynucleotide is a polynucleotide constituted of a sequence having a sequence identity of at least 90%, preferably 95%, more preferably 98%, and even more preferably 99% with the nucleotide sequence indicated in (a) or (b) and is capable of functioning in the same manner as (a) or (b), that is, is capable of suppressing proliferation specifically in normal cells when inserted in each position of the CVB3-WT genome to arrange the gene-modified coxsackievirus.
Methods for obtaining a polynucleotide having a sequence with which one to several nucleotides are deleted, substituted, or added with respect to a certain nucleotide sequence and methods for calculating sequence identity related to a nucleotide sequence (for example, sequence identity can be calculated using a BLAST algorithm) is well known to those skilled in the art. The same applies to nucleotide sequences indicated below.
Also, from a standpoint of reducing undesirable actions of CVB3-WT in respective tissues, the tissue-specific miRNA (and its target sequence) used in the present invention may include at least one of miR-1 and miR-217. miR-217 is said to be expressed specifically in the pancreas and miR-1 is said to be expressed specifically in muscle tissue and normal cells. miR-1 and miR-217 are used in combination with at least one of miR-34a and miR-34c. Also, miR-1 and miR-217 may be combined.
Although any number can be selected as the number of inserted target sequences for miR-1 or miR-217 as long as the intended effects are exhibited, it is preferably plural, for example, two to six.
Also, in another especially preferable aspect, the inserted polynucleotide is (c) or (d) shown below. Or, it is a polynucleotide constituted of a sequence with which one to several nucleotides are deleted, substituted, or added with respect to (c) or (d) and is capable of functioning in the same manner as (c) or (d), that is, is capable of suppressing proliferation specifically in normal cells when inserted in at least one of between the positions 742 and 743 of the CVB3-WT genome (5′ UTR region), between the positions 7304 and 7305 of the CVB3-WT genome (3′ UTR region), and each of between the positions 742 and 743 of the CVB3-WT genome (5′ UTR region) and between the positions 7304 and 7305 of the CVB3-WT genome (3′ UTR region) to arrange the gene-modified coxsackievirus. Also, the inserted polynucleotide is capable of suppressing proliferation tissue-specifically in the pancreas (see
Also, in another especially preferable aspect, the inserted polynucleotide is (e) or (f) shown below. Or, it is a polynucleotide constituted of a sequence with which one to several nucleotides are deleted, substituted, or added with respect to (e) or (f) and is capable of functioning in the same manner as (e) or (f), that is, is capable of suppressing proliferation specifically in normal cells and tissue when inserted in at least one of between the positions 742 and 743 of the CVB3-WT genome (5′ UTR region), between the positions 7304 and 7305 of the CVB3-WT genome (3′ UTR region), and each of between the positions 742 and 743 of the CVB3-WT genome (5′ UTR region) and between the positions 7304 and 7305 of the CVB3-WT genome (3′ UTR region) to arrange the gene-modified coxsackievirus. Also, the inserted polynucleotide is capable of suppressing proliferation tissue-specifically in muscle tissue. Or, the inserted polynucleotide is a polynucleotide constituted of a sequence having a sequence identity of at least 90%, preferably 95%, more preferably 98%, and even more preferably 99% with the nucleotide sequence indicated in (e) or (f) and is capable of functioning in the same manner as (e) or (f), that is, is capable of suppressing proliferation specifically in normal cells when inserted in each position of the CVB3-WT genome to arrange the gene-modified coxsackievirus. Also, the inserted polynucleotide is capable of suppressing proliferation tissue-specifically in muscle tissue.
[Preparation of Gene-Modified Virus, Etc.]
The gene-modified virus of the present invention can be prepared by genetically manipulating CVB3-WT. CVB3-WT can be isolated from a sample or the like by a known virus isolation method. Examples of the virus isolation method include centrifugation, proliferation of the virus in cultured cells, and so forth. Once the gene-modified coxsackievirus is prepared, the gene-modified coxsackievirus can be proliferated using various molecular biological methods for virus production.
CVB3 that is to be the starting point of gene-modification may be biologically selected by culturing a naturally occurring virus over several passages in a cell line such that the virus acquires a high infectivity for cancer cells. Examples of a cell line suitable for the biological selection include cancer cell lines that express CAR, DAF, and so forth.
For evaluation of the gene-modified coxsackievirus prepared according to the present invention, various aspects, such as safety, efficacy, and titer, can be evaluated by various in vitro or in vivo means well known to those skilled in the art. For example, aggressiveness against cancer cells (oncolytic property or cytotoxicity) can be confirmed by testing survival of a cancer cell line exposed to CVB3. Examples of a method for testing the survival of a cell line include a method of staining fixed cells with a staining solution and quantifying the number of stained live cells, a crystal violet method, a method of quantifying an apoptosis-specific marker, and so forth. As a result of using any of the aforementioned methods on a cell line of cancer cells incubated with CVB3 to quantify the cancer cells surviving after a predetermined time, the cancer cells killed by the cytotoxicity due to infection by CVB3 can be quantified.
When, in regard to measurements of production and titer of the gene-modified CVB3 (inserted with the target sequence for miR-34a or the target sequence for miR-34c), the present inventors measured the virus titer in H1299 cells using the gene-modified CVB3 produced in H1299 cells, the results indicated that, although its virus titer is slightly lower than the virus titer of CVB3-WT, the gene-modified CVB3 has a sufficient virus titer (see
[Pharmaceutical Composition]
One aspect of a pharmaceutical composition provided by the present invention contains the above-described gene-modified CVB3 as an active ingredient. The types of cancer to be an object of treatment with the pharmaceutical composition are not particularly limited and include solid cancers and fluid cancers. CVB3 has cytotoxicity against cancer cells of solid cancers and fluid cancers. The cytotoxicity of CVB3 against cancer cells is based on lysis of cancer cells upon infection of the cancer cells and replication in the cytoplasm of the cancer cells by the virus or on apoptosis induced by activation of caspase in the cancer cells caused by infection by the virus. CVB3 can recognize CAR on the cell surface and infect the cell. “Treatment (to treat)” as referred to in the present invention in relation to a disease or condition includes preventive treatment and curative treatment.
CVB3 has cytotoxicity against cancer cells of solid cancers and fluid cancers, and in regard to solid cancers, cancer cells with which especially potent cytotoxicity is induced are cells of a cancer selected from the group consisting of small cell lung cancer, non-small cell lung cancer, lung squamous cell cancer, malignant mesothelioma, colon cancer, colorectal cancer, esophageal cancer, hypopharyngeal cancer, human B lymphoma, breast cancer, and uterine cervix cancer. The pharmaceutical composition according to the present embodiment is thus preferably applied to a cancer selected from the group consisting of small cell lung cancer, non-small cell lung cancer, lung squamous cell cancer, malignant mesothelioma, colon cancer, colorectal cancer, esophageal cancer, hypopharyngeal cancer, human B lymphoma, breast cancer, and uterine cervix cancer as an object of treatment.
Lung cancer is a cancer with which the number of affected individuals is of high rank. The pharmaceutical composition according to the present embodiment can contribute to the treatment of more lung cancer patients. In Japan, where Western eating habits are established, colon cancer and colorectal cancer morbidities are increasing and mortalities of these cancers are also increasing. The pharmaceutical composition according to the present embodiment increases the choices of curative drugs for colon cancer and colorectal cancer, and this is beneficial for the patients. The recurrence rate of esophageal cancer after surgical resection is as high as 30 to 50%, and the sensitivity thereof to existing drugs is low. The pharmaceutical composition according to the present embodiment can be anticipated to improve treatment results of esophageal cancer.
Also, the pharmaceutical composition according to the present embodiment exhibits potent cytotoxicity against CDDP-resistant, gefitinib-resistant, or oxaliplatin-resistant cancer cells. Therefore, a treatment that is effective against so-called intractable cancers that exhibit resistance to these anticancer agents can be provided.
When containing CVB3, the pharmaceutical composition according to the present embodiment exhibits potent cytotoxicity also against cancer stem cells. Cancer stem cells are considered to be one of the causes of relapse of cancer, and the composition is thus useful for prevention of metastasis and relapse of cancer.
<Dosage Form, Usage, and Dosage>
Also, the pharmaceutical composition according to the present embodiment can be adopted in various dosage forms and various administration routes. That is, the pharmaceutical composition according to the present embodiment can also be a topical preparation or a preparation for systemic administration. For example, it can be arranged as an injection or a drip and administered by intratumoral administration, intravenous administration, intrathoracic administration, or intraperitoneal administration in accordance with the type of cancer. In particular, in many cases of gastrointestinal cancers, such as esophageal cancer and colon cancer, the pharmaceutical composition can be injected directly into a tumor tissue while visually observing the tumor tissue with an endoscope or the like. In such a case, since the injection site can be confirmed with the endoscope or the like, there is also provided an advantage that even if bleeding occurs, it is easily treated. Besides the above, the composition may be administered orally or it may be administered intramuscularly or subcutaneously or via the rectum, vagina, nasal cavity, or the like.
The pharmaceutical composition according to the present embodiment may be arranged to contain a carrier, diluent, auxiliary agent, and so forth in addition to the gene-modified CVB3. As the carrier, for example, a liposome, micelle, and so forth are preferred. The liposome contains a combination of a lipid with a steroid or a steroid precursor that contributes to membrane stability. As the lipid in this case, a phosphatidyl compound, such as phosphatidylglycerol, phosphatidylcholine, phosphatidylserine, sphingolipid, phosphatidylethanolamine, cerebroside, and ganglioside, can be cited. CVB3 coated with the liposome or micelle can reduce the immune response of a host.
As examples of the diluent, desalted water, distilled water, physiological saline, and so forth can be cited. As examples of the auxiliary agent, vegetable oils, cellulose derivatives, polyethylene glycol, fatty acid esters, and so forth can be cited.
In the case of oral administration, the pharmaceutical composition may contain a sweetener, disintegrating agent, diluent, coating agent, preservative, and so forth.
The pharmaceutical composition according to the present embodiment is administered such that an amount of CVB3 would be sufficient for treatment of cancer. A dosage is determined based on body weight, age, and sex of a patient, size of tumor tissue, and so forth. For example, when the pharmaceutical composition is arranged as a liquid preparation, it is sufficient that 1×102 to 1×1010 TCID50 (50% tissue culture infectious dose) of CVB3 is contained in 1 ml of the liquid formulation. Preferably, it is sufficient that 1×105 TCID50 or more of CVB3 is contained in 1 ml of the liquid preparation. The pharmaceutical composition may be administered in one dose or may be administered over a plurality of doses. The pharmaceutical composition may be continuously administered as a sustained release preparation.
<Combined Use with Other Preparations>
The pharmaceutical composition according to the present embodiment may be used in combination with an anticancer agent. By combined use with the anticancer agent that differs in action mechanism from the pharmaceutical composition, improvement in antitumor effect can be anticipated. The anticancer agent is not particularly limited, and those used for treatment of small cell lung cancer, non-small cell lung cancer, lung squamous cell cancer, malignant mesothelioma, colon cancer, colorectal cancer, esophageal cancer, hypopharyngeal cancer, human B lymphoma, uterine cervix cancer, pancreatic cancer, and so forth are desirable. Specific anticancer agents include CDDP (cisplatin), gefitinib, oxaliplatin, and so forth.
[Others]
The pharmaceutical composition according to the embodiment of the present invention may contain, as an active ingredient, a polynucleotide derived from CVB3 (including the gene-modified CVB3; the same applies below) capable of infecting cancer cells. The CVB3-derived polynucleotide may be a virus RNA directly isolated from CVB3, a synthetic RNA, or a cDNA corresponding to abase sequence of an isolated virus RNA, respectively. Any method can be used to isolate the virus RNA. Examples of the method for isolating the virus RNA include a method based on use of phenol/chloroform extraction and so forth. Also, the polynucleotide may be a virus plasmid or an expression vector containing a polynucleotide for producing a virus. The expression vector includes, for example, a plasmid that can express an RNA encoding a virus protein required for producing the virus. The expression vector may contain a transcription regulatory/control sequence that is functionally ligated with the inserted polynucleotide. The transcription regulatory/control sequence referred to here is, for example, a promoter for initiating transcription, an expression control element for enabling binding of a ribosome to a transcribed mRNA, and so forth.
As the expression vector, for example, pSV2neo, pEF-PGKpuro, pTk2, non-replicating adenovirus shuttle vector, cytomegalovirus promoter, and so forth can be used. The cDNA that encodes the virus protein required for producing the virus can be prepared by reverse transcription of the virus RNA or a fragment thereof.
The pharmaceutical composition according to the present embodiment may contain, for example, a carrier such as a liposome, in addition to the polynucleotide derived from CVB3 capable of infecting cancer cells. The polynucleotide derived from CVB3 may contain, for example, the polynucleotide constituted of the sequence of SEQ ID NO: 1 or 2, and/or the polynucleotide constituted of any of the sequences of SEQ ID NOS: 3 to 8, 19, 20, 25, and 26.
Examples of the present invention shall now be described. However, the scope of the present invention is not limited by these examples.
The contents shown in Table 1 below are given as an example of kinds of target sequences for the tissue-specific miRNAs in the present invention and positions in the CVB3-WT genome at which the target sequences are inserted.
To describe the contents of Table 1, No., name of virus, kind of target sequence inserted between the positions 742 and 743 bp inside the genome 5′ untranslated region (UTR) of CVB3-WT, and kind of target sequence inserted between the positions 7304 and 7305 bp inside the genome 3′ untranslated region (UTR) of CVB3-WT are indicated from the left side of the table. For example, the virus of No. 7 (CVB3-34a&217T-53) is a modified virus with which a polynucleotide combining two target sequences for miR-34a and two target sequences for miR-217 is inserted in each of between the positions 742-743 bp inside the 5′ UTR and between the positions 7304 and 7305 bp inside the 3′ UTR. As the target sequences, a total of eight miRNA target sequences are inserted onto the genome. That is, the two target sequences for miR-34a and the two target sequences for miR-217 are inserted between the positions 742-743 bp inside the 5′ UTR. Also, the two target sequences for miR-34a and the two target sequences for miR-217 are inserted between the positions 7304 and 7305 bp inside the 3′ UTR.
I. Improvement in Safety of CVB3 by Insertion of miRNA Target Sequence
An object of the present research is to suppress proliferation of a gene-modified virus of oncolytic wild-type CVB3 (CVB-WT) in normal cells. The inventors inserted a target sequence for miR-34a or miR-34c in the genome 3′ untranslated region (UTR) of the CVB3-WT, in particular, between 7304 and 7305 bp of the CVB3 genome to prepare a gene-modified virus. Also, the inventors inserted the target sequence for miR-34a or miR-34c in the genome 5′ untranslated region (UTR) of the CVB3-WT, in particular, between 742 and 743 bp of the CVB3 genome to prepare a gene-modified virus. Further, the inventors inserted four target sequences for miR-34a or miR-34c or inserted a polynucleotide combining two target sequences for miR-34a and two target sequences for miR-217 in each of between the positions 742 and 743 bp inside the 5′ UTR and between the positions 7304 and 7305 bp inside the 3′ UTR of the CVB3-WT genome to prepare a gene-modified virus. A RISC complex having miR-34a, miR-34c, or miR-217 that is highly expressed in normal cells binds to the inserted target sequence for miR-34a, miR-34c, or miR-217 to inhibit translation of the virus protein and so forth to enable suppression of proliferation inside the normal cells.
I-1. Insertion of Target Sequences into CVB3 Genome and Virus Titers
The inventors made note of two miRNAs, namely, miR-34a and miR-34c that constitute the miR-34 family with which high expression is seen in normal cells all over the body and prepared two kinds of miRNA target sequences in each of which four target sequences for one of the miRNAs are ligated consecutively (miR-34aT×4+(miR-34aT×4-) and miR-34cT×4+(miR-34cT×4−)).
Also, an miRNA target sequence combining two target sequences for miR-34a and two target sequences for miR-217 (miR-34aT×2&miR-217T×2+(miR-34aT×2&miR-217T×2−)) was prepared.
The target sequence for miR-34a and the target sequence for miR-34c were respectively inserted between 7304 and 7305 bp of the CVB3 genome. Also, the target sequence for miR-34a and the target sequence for miR-34c were respectively inserted between 742 and 743 bp of the CVB3 genome. Further, the target sequence for miR-34a and miR-217 was inserted in each of between 742 and 743 bp of the CVB3 genome and between 7304 and 7305 bp of the CVB3 genome. The insertion of the target sequences into the genome was performed using the In-Fusion cloning (TaKaRa Inc.) method (see
Hereinafter, unless noted in particular otherwise,
CVB3-34aT-3 refers to a virus in which four target sequences for miR-34a (the polynucleotide of SEQ ID NO: 3) are inserted in the 3′ UTR, and
CVB3-34cT-3 refers to a virus in which four target sequences for miR-34c (the polynucleotide of SEQ ID NO: 4) are inserted in the 3′ UTR.
Also, CVB3-34aT-5 refers to a virus in which four target sequences for miR-34a (the polynucleotide of SEQ ID NO: 3) are inserted in the 5′ UTR, and
CVB3-34aT-53 refers to a virus in which four target sequences for miR-34a (the polynucleotide of SEQ ID NO: 3) are inserted in each of the 5′ UTR and the 3′ UTR.
Further, CVB3-34a&217T-53 refers to a virus in which a polynucleotide constituted of two target sequences for miR-34a and two target sequences of miR-217 (the polynucleotide of SEQ ID NO: 25) is inserted in each of the 5′ UTR and the 3′ UTR.
Also, CVB3-1&217T refers to the virus in which a polynucleotide constituted of two target sequences for miR-1 and two target sequences of miR-217 (the polynucleotide of SEQ ID NO: 29) is inserted in the 3′ UTR.
Next, to evaluate virus titers of the gene-modified CVB3s, the virus titers were compared with that of CVB-WT. Here, virus production and titer were measured using H1299 cells. In more detail, the respective viruses of CVB3-WT, CVB3-34aT-3, and CVB3-34cT-3 were introduced into a non-virus-infected H1299 cell line to produce viruses. The produced viruses were recovered and a non-virus-infected H1299 cell line was infected therewith again to measure the virus titers. The respective virus titers of CVB3-34aT-3 and CVB3-34cT-3 in the H1299 cells, although slightly lower than the virus titer of CVB-WT, were of TCID50/ml values exceeding 1.0×108 and it was thus made clear that the viruses have sufficient titers to be subject to nonclinical tests (see
I-2. Evaluation of Oncolytic Activities of Gene-Modified Viruses with Respect to Cancer Cells and Normal Cells
Next, it was evaluated whether or not the respective viruses of CVB3-WT, CVB3-34aT-3, and CVB3-34cT-3 proliferate and have oncolytic effects in various cancer cells and normal cells. As the cancer cells, lung cancer cell lines of NSCLC (A549 cells and H1299 cells), a pancreatic cancer cell line of AsPC-1 cells, and a breast cancer cell line of ZR-75-1 cells were used, and as the normal cells, BEAS-2B cells, which are normal tracheal epithelial cells, and Het-1A cells, which are normal esophagus squamous cells, were used.
Consequently, results indicating that CVB3-34aT-3 and CVB3-34cT-3 exhibit sufficient oncolytic effects in the respective cancer cells were obtained (see
From the above, it was made clear that CVB3-34aT-3 and CVB3-34cT-3 are capable of virus proliferation and exhibit oncolytic effects in the cancer cells. It was also made clear that these viruses, unlike CVB3-WT, do not exhibit oncolytic effects and are suppressed in virus proliferation in the normal cells.
Next, it was evaluated whether or not the respective viruses of CVB3-WT, CVB3-34aT-3, CVB3-34aT-5, CVB3-34aT-53, and CVB3-34a&217T-53 proliferate and have oncolytic effects in various cancer cells and normal cells. As the cancer cells, the abovementioned NSCLC (H1299 cells: ordinary) and NSCLC forcibly made by a known method to express miR-34a highly (H1299 cells: high expression) were used, and as the normal cells, the abovementioned BEAS-2B cells were used. In regard to the preparation of the H1299 cells forcibly made to express miR-34a highly, a known method was used and description of the preparation method shall thus be omitted.
Consequently, results indicating that the respective viruses exhibit sufficient oncolytic effects in the ordinary H1299 cells were obtained (see upper diagram in
From the above, it was made clear that CVB3-34aT-3, CVB3-34aT-5, CVB3-34aT-53, and CVB3-34a&217T-53 are capable of virus proliferation and exhibit oncolytic effects in the cancer cells. It was further made clear that these viruses, unlike CVB3-WT, do not exhibit oncolytic effects and are suppressed in virus proliferation in cancer cells forcibly made to express miR-34a highly and in the normal cells.
Next, it was evaluated whether or not the respective viruses of CVB3-WT, miR-1&217T, CVB3-34aT-3, and CVB3-34cT-3 proliferate and have oncolytic effects in various cancer cells and normal cells. As the cancer cells, the abovementioned NSCLC (H1299 cells) was used, and as the normal cells, the BEAS-2B cells were used.
Consequently, results indicating that the respective viruses exhibit sufficient oncolytic effects in the H1299 cells were obtained (see left diagram in
From the above, it was made clear that CVB3-34aT-3 and CVB3-34cT-3 are capable of virus proliferation and exhibit oncolytic effects in the cancer cells. It was further made clear that, unlike miR-1&217T and CVB3-WT, CVB3-34aT-3 and CVB3-34cT-3 do not exhibit oncolytic effects and are suppressed in virus proliferation in the normal cells.
Next, cell viability tests of cancer cells and normal cells infected with the respective viruses of CVB3-WT, CVB3-34aT-3, and CVB3-34cT-3 were evaluated by an MTS method. Non-virus-infected H1299 cells (1.0×104 cells) were infected with the respective viruses of CVB3-WT, CVB3-34aT-3, and CVB3-34cT-3 produced in H1299 cells and cell viabilities after 24 hours, after 48 hours, and after 72 hours were measured. In the test with MOI=0.001, the H1299 cells were substantially killed after 72 hours by all of CVB3-WT, CVB3-34aT-3, and CVB3-34cT-3 (see
Also, non-virus-infected BEAS-2B cells (1.0×104 cells) were infected with the respective viruses of CVB3-WT, CVB3-34aT-3, and CVB3-34cT-3 produced in H1299 cells and the cell viabilities after 24 hours, after 48 hours, and after 72 hours were measured. In the test with MOI=0.01, whereas BEAS-2B cells were substantially killed after 72 hours by CVB3-WT, survival of the BEAS-2B cells after 72 hours was confirmed with CVB3-34aT-3 and CVB3-34cT-3 (see
From the above, it was made clear that CVB3-34aT-3 and CVB3-34cT-3 are capable of virus proliferation and exhibit oncolytic effects in the cancer cells. It was also made clear that these viruses, unlike CVB3-WT, are suppressed in virus proliferation and strongly suppressed in cytotoxicity in the normal cells.
Further, the cell viabilities after 72 hours of BEAS-2B cells (1.0×104 cells) and Het-1A cells ((1.0×104 cells) are shown in
As shown in
Next, the following
As shown in
Next, the following
As shown in
I-3. Tumorigenesis Test Using Mice (In Vivo)
Next, mice were administered with a cancer cell line (H1299) to form tumors, the respective viruses of CVB3-WT, CVB3-34aT-3, and CVB3-34cT-3 were administered into the tumors, and changes in the tumors were observed. Although detailed test contents shall be described later, observation was performed over a fixed period and tumor volumes (see
Consequently, the results that, with the mice of the untreated group (untreated), the tumor volume increases with time from the day of administration of the cancer cell line (H1299) were observed as shown in
Further, as shown in
From the above results, it was made clear, even in the in vivo tests using mice, that the respective viruses of CVB3-34aT-3 and CVB3-34cT-3 exhibit the same oncolytic effects as CVB3-WT against a human lung cancer cell line (H1299). Also, a temporary decrease in body weight, which occurred with mice administered with CVB3-WT, did not occur with the mice administered with the respective viruses of CVB3-34aT-3 and CVB3-34cT-3, and the results thus suggested a possibility that the occurrence of a side effect is suppressed.
I-4. Blood Biochemical Examination Using Mice (In Vivo)
Next, mice were administered with a cancer cell line (H1299) to form tumors, and upon administering the respective viruses of CVB3-WT, CVB3-34a&217T-53, and miR-1&217T into the tumors, blood was sampled from mice of one-dose groups and mice of a two-dose groups of the respective viruses and a blood biochemical examination was performed. Although details shall be described later, in the blood biochemical examination, respective component amounts in blood of GOP/AST (liver and myocardium), LDH (liver, myocardium, and kidneys), GPT/ALT (liver and myocardium), and Amy (pancreas), which are markers of side effects caused by administration of CVB3-WT, were measured with a dry clinical chemical analyzer to evaluate whether or not there were side effects. With the mice of the one-dose group, the viruses were administered into the tumors on the second day from the day of administration of the cancer cell line (H1299) and blood was sampled from the mice two days later. Also, with the mice of the two-dose group, the viruses were administered into the tumors on the second day and the fourth day from the day of administration of the cancer cell line (H1299) and blood was sampled from the mice two more days later. The study was performed with a sample number n=3 or 4 for each virus or control.
Consequently, as shown in
Also,
CVB3-34a&217T-53, component amounts of the respective markers of approximately the same levels as or not more than the control were indicated.
The above results show that, in the blood biochemical examination using mice, the occurrence of side effects, which occurred in the mice administered with CVB3-WT, was suppressed in the mice administered with CVB3-34a&217T-53 and CVB3-34aT-53. Also, comparing CVB3-34a&217T-53 and miR-1&217T, it was made clear that CVB3-34a&217T-53 is more likely to suppress the occurrence of side effects. Further, comparing CVB3-34a&217T-53 and CVB3-34aT-53, it was made clear that CVB3-34a&217T-53 is even more likely to suppress the occurrence of side effects.
I-5. Comparison of 5′ UTR and 3′ UTR as Insertion Positions for Target Sequences
Next, respective target sequences were inserted in the 5′ UTR (between the positions 742 and 743 bp) and the 3′ UTR (between the positions 7304 and 7305 bp) and target-sequence-inserted viruses were subcultured three times or six times to confirm whether or not the target sequences became detached from the genome and evaluate retention stabilities of the target sequences. A base length of the CVB3 genome is approximately 400 bp and a base length with the respective target sequences inserted in the CVB3 genome is approximately 500 bp. The CVB3 genomes extracted from respective samples were electrophoresed by a known electrophoresis method and the base lengths were confirmed. That is, if detachment of the target sequences from the CVB genome occurred, the base length is confirmed to be approximately 400 bp.
Electrophoresis results of electrophoresing products obtained using a genome extracted from CVB3-WT that is not inserted with any target sequence and genomes extracted from CVB3-34aT-3 and CVB3-34cT-3 that were subcultured three times and amplifying vicinities of the target sequence insertion sites by a PCR reaction are schematically shown in
Also, electrophoresis results of electrophoresing products obtained using genomes extracted from CVB3-WT that is not inserted with any target sequence and genomes extracted from viruses that were inserted with the respective target sequences and were subcultured three, six, and ten times and amplifying vicinities of the target sequence insertion sites by the PCR reaction are schematically shown in
Consequently, it was made clear from
Also, from
I-6. Methods Summary
The present study was carried out in accordance with the following protocols.
[Preparation of Respective Gene-Modified Viruses]
(Methods)
1. Mix the following reagents in the following order in a 0.2 ml PCR tube on ice.
2. Stir by tapping or gentle pipetting, spin down lightly, and collect the solution. Execute the following program with a thermal cycler made by Eppendorf AG.
3. (1) miR-34aT: 94° C. 2:00, 98° C. 0:10, 60° C. 0:30, 68° C. 6:30 (28 cycles), 72° C. 7:00
(2) miR-34cT: 94° C. 2:00, 98° C. 0:10, 57° C. 0:30, 68° C. 6:30 (28 cycles), 72° C. 7:00
4. Purify the PCR products and perform restriction enzyme treatment with Dpn I for 1 hour.
5. Perform agarose gel electrophoresis using the restriction enzyme treatment products and cut out the target bands.
6. Prepare double-strand inserts. Place 1 μl each of SEQ ID NOS: 3 and 11 or SEQ ID NOS: 4 and 14 in a tube, heat in annealing buffer at 94° C. for 10:00, cool to 25° C. at −1° C./1 min, and let react at 25° C. for 5:00.
7. After gel purification and then after restriction enzyme treatment, use In-fusion to let CVB3 plasmid (150 ng) and the double-strand insert (60 ng) react at 50° C. for 15 min.
8. Introduce the In-fusion product into competent cells and culture at 37° C.
9. On the next day, pick up the colonies and culture in an LB medium.
10. Recover the plasmid from the culture and check whether or not the miRNA target sequences have been inserted.
<Virus RNA Preparation>
(Methods)
1. Mix the following reagents in the following order in a 0.2 ml PCR tube at room temperature (total: 20 μl).
2. Let react at 37° C. for 3 h in a thermal cycler (use thermal cycler made by Bio-Rad Inc.).
3. After 3 h, add 1 μl of TURBO DNase into the tube in reaction, stir well, and let react additionally at 37° C. for 15 min.
4. Prepare in advance 1.1 times the number of reaction tubes of solutions, with each of which 114 μl of UltraPure and 15 μl of the accessory Ammonium Acetate Stop Solution are mixed in a 1.5 ml tube.
5. After the reaction, add 129 μl of the abovementioned mixed solution into the reaction tube and then perform pipetting.
6. Transfer the entire amount into a 0.7 ml tube.
7. Add 150 μl of Phenol:Chloroform thereto and then perform pipetting and mixing by inverting.
8. Centrifuge at 10,000×g for 2 min at room temperature.
9. Transfer the supernatant (approx. 150 μl) into a separate, new 0.7 ml tube.
10. Add 150 μl of Chloroform to the aqueous layer and then mix by inverting.
21. Centrifuge at 10,000×g for 2 min at room temperature.
22. Transfer the supernatant (approx. 100 μl) into a separate, new 0.7 ml tube.
23. Add 150 μl of cold 5M Ammonium acetate to the aqueous layer and then perform pipetting.
24. Leave to stand on ice for 10 min.
26. Use a Pipetman to slowly remove the supernatant.
29. Use a Pipetman to slowly remove the supernatant as much as possible.
30. Add 70 μl of UltraPure to the pellet and dissolve.
<Virus Preparation>
(Methods)
1. To dispensed Opti-MEM, add RNA to 80 μg into the liquid, and to Opti-MEM dispensed in a separate tube, add 120 μl of Lipofectamine 2000 into the liquid.
2. Let both stand for 5 min at room temperature.
3. Mix both tubes and let stand for 20 min at room temperature.
4. After 20 min, add the entire amount of the mixed solution to NCI-H1299 cells.
5. After 4 h, replace with growth medium.
6. Incubate at 37° C. under 5% CO2 for 24 h.
7. After 25 h from transfection, use a cell scraper to peel off the respective NCI-H1299 cells without discarding the medium.
8. Recover the supernatant, together with the cells, into a 50 ml tube.
9. Immerse the 50 ml tube in liquid N2 to freeze.
10. Thaw with a water bath at 37° C.
11. Repeat the freezing and thawing of 9 and 10 two times (freezing and thawing are performed a total of three times).
13. Replace the NCI-H1299 cell medium onto which the supernatant is to be transferred with fresh medium (15 ml).
14. Add the entire amount of the supernatant after centrifugation to the NCI-H1299 cells.
15. Incubate at 37° C. under 5% CO2 for 6 to 8 h.
16. When CPE is confirmed in 60 to 70% or more, remove the culture supernatant.
17. Add 2 ml of Opti-MEM (registered trademark) I.
18. Peel off the cells with a cell scraper.
19. Recover the entire amount of Opti-MEM (registered trademark) I together with the cells into a 15 ml tube.
20. Immerse this 15 ml tube in liquid nitrogen and freeze (approx. 2 min).
21. Thaw with a water bath at 37° C. (approx. 10 min).
22. Repeat the freezing and thawing of 20 and 21 two times (freezing and thawing are performed a total of three times).
24. Preserve the supernatant at −80° C.
<Virus Titer Measurement>
(Methods)
1. Inoculate the NCI-H1299 cells into all wells of the 96 well Flat plate at 5×103 cells/100 μl/well.
2. Incubate at 37° C. under 5% CO2 for 7 h.
3. Add 180 μl of Opti-MEM to each well from the second column to the last, twelfth column of the 96 well Round plate.
4. For the first column that is the highest virus concentration column (ordinarily 10−2), add 990 μl of Opti-MEM into a 1.5 ml tube, add 10 μl of the virus stock solution thereto, and perform adequate pipetting to prepare the 102 solution.
5. Add 120 μl of the virus 10−2 column solution to each well of the first column of the 96 well Round plate.
6. Use an 8-channel electronic pipette to transfer 20 μl of the first column virus solution to each well of the second column.
7. Perform pipetting once at this point and then change the tip.
8. Take 20 μl from each well of the column diluted immediately before and transfer to each well of the adjacent column.
9. Perform pipetting once and then change the tip.
10. Repeat 8. and 9. until the eleventh column.
11. Take out the Flat plate inoculated with the NCI-H1299 cells from the incubator.
12. Use an 8-channel pipette to add 50 μl of the solution of each well of each column of the Round plate, starting from the dilute twelfth column, to the NCI-H1299 cells in the Flat Plate.
13. Incubate at 37° C. under 5% CO2 for 120 h (5 days).
14. Count the wells in which 50% CPE is seen. Calculate the titer using the following formula.
Log 10(TCID50)=L+d(S−0.5)+log 10(1/v)
<Cell Viability Measurement>
(Methods)
1. Inoculate the NCI-H1299, BEAS-2B, and Het-1A cells into the 96 well Flat plate at 1×104 cells/80 μl/well.
2. Incubate at 37° C. under 5% CO2 for 7 h.
3. Dilute the viruses with Opti-MEM to MOI=0.1 or MOI=1.
4. Place 2011 of the diluted virus solutions in each well.
5. After 24, 48, and 72 hours, place 20 μl of the CellTiter 96 Reagent in each well, incubate for 1 hour, and measure the absorbance at 490 nm with Enspire.
<Tumorigenesis Test (In Vivo)>
(Methods)
1. Day 0: Administer 0.1 ml/10 g (body weight) of a triple anesthetic combination (medetomidine hydrochloride 0.3 g+midazolam 4 mg+butorphanol tartrate 5 mg/kg anesthetic combination) into the abdominal cavity of each mouse with a 26 G needle. Subcutaneously administer 5×106 cells/100 μl PBS/mouse of cancer cells of the cancer cell line (H1299) to the right abdominal region or left abdominal region of each mouse with a 27 G needle.
2. Day 2: Observe every other day and when the long diameter of a tumor of a mouse of the untreated group reaches 0.4 cm, disinfect the administration site with ethanol and thereupon administer 50 μl Opti-MEM/mouse into the tumor with a 29 G needle (alternate day administration; maximum of five times: day 2, 4, 6, 8, and 10).
3. Day 2: When the long diameter of a tumor of a mouse of a treated group reaches 0.4 cm, disinfect the administration site with ethanol and thereupon administer CVB3-WT or gene-modified CVB3 (CVB3-34aT-3 or CVB3-34cT-3) at 5×106 TCID50/50 μl Opti-MEM/mouse into the tumor with a 29 G needle inside a safety cabinet (alternate day administration; maximum of five times: day 2, 4, 6, 8, and 10).
4. Measure the body weight and the tumor diameter every other day, and euthanize immediately when the tumor long diameter exceeds 10 mm or the tumor becomes an ulcer (tumor volume=long diameter×short diameter×short diameter/2).
5. Even with a mouse for which a tumor does not form even after the elapse of three weeks or a tumor is completely rejected, set an observation period of up to 150 days maximum and then euthanize immediately.
<Blood Biochemical Examination (In Vivo)>
(Methods)
1. Day 0: Administer 0.1 ml/10 g (body weight) of a triple anesthetic combination (medetomidine hydrochloride 0.3 g+midazolam 4 mg+butorphanol tartrate 5 mg/kg anesthetic combination) into the abdominal cavity of each mouse with a 26 G needle. Subcutaneously administer 5×106 cells/100 μl PBS/mouse of cancer cells of the cancer cell line (H1299) to the right abdominal region or left abdominal region of each mouse with a 27 G needle.
2. Day 2: Observe every other day and when the long diameter of a tumor of a mouse of the untreated group reaches 0.4 cm, disinfect the administration site with ethanol and thereupon administer 50 μl Opti-MEM/mouse into the tumor with a 29 G needle.
3. Day 2: When the long diameter of a tumor of a mouse of a treated group reaches 0.4 cm, disinfect the administration site with ethanol and thereupon administer CVB3-WT or gene-modified CVB3 (CVB3-34a&217T-53 or miR-1&217T) at 5×106 TCID50/50 μl Opti-MEM/mouse into the tumor with a 29 G needle inside a safety cabinet.
4. (For the one-dose group) Day 4: Administer 0.1 ml/10 g (body weight) of the triple anesthetic combination into the abdominal cavity of each mouse with a 26 G needle. Dissect the mouse and collect blood from the inferior vena cava with a 24 G needle (approx. 600 mL).
5. (For the two-dose group,) administer Opti-MEM or the virus into the tumor of each mouse one more time with a 29 G needle on day 4. Collect blood on day 6.
6. Leave the blood at room temperature for one hour (to coagulate) and then centrifuge at 1,500×g at room temperature for 15 minutes.
7. Transfer the supernatant (serum) into a new 1.5 mL tube.
8. Perform blood biochemical examination with Spot-Chem (registered trademark).
SEQ ID NO:1: miR-34a
SEQ ID NO:2: miR-34c
SEQ ID NO:3: miR-34aT×4+
SEQ ID NO:4: miR-34cT×4+
SEQ ID NO:5: miR-34aT×2 & miR-217T×2+
SEQ ID NO:6: miR-34cT×2 & miR-217T×2+
SEQ ID NO:7: miR-34aT×2 & miR-1T×2+
SEQ ID NO:8: miR-34cT×2 & miR-1T×2+
SEQ ID NO:9: miR-34a-Inverse Forward
SEQ ID NO:10: miR-34a-Inverse Reverse
SEQ ID NO:11: miR-34aT×4−
SEQ ID NO:12: miR-34c-Inverse Forward
SEQ ID NO:13: miR-34c-Inverse Reverse
SEQ ID NO:14: miR-34cT×4−
SEQ ID NO:25: miR-34a×2 & miR-217×2+
SEQ ID NO:26: miR-34a×2 & miR-217×2−
SEQ ID NO:29: miR-1&217T Forward
SEQ ID NO:30: miR-1&217T Reverse
| Number | Date | Country | Kind |
|---|---|---|---|
| 2017-083019 | Apr 2017 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2018/015986 | 4/18/2018 | WO | 00 |
