The present invention relates to the use of butylidenephthalide (BP), including the prevention, mitigation and/or inhibition of the growth, migration, invasion and/or metastasis of cancer stem cells (CSCs), particularly oral cancer stem cells, nasopharyngeal cancer stem cells, esophageal cancer stem cells, myeloma stem cells, skin cancer stem cells, melanoma stem cells, thyroid cancer stem cells, lymphoma stem cells, leukemia stem cells, breast cancer stem cells, bladder cancer stem cells, ovarian cancer stem cells, cervical cancer stem cells, prostate cancer stem cells, gastric cancer stem cells, liver cancer stem cells, lung cancer stem cells, colon cancer stem cells, rectal cancer stem cells, pancreatic cancer stem cells, gall bladder cancer stem cells, renal cancer stem cells, glioblastoma stem cells, thymic carcinoma stem cells, rhabdomyosarcoma stem cells, brain tumor stem cells and medulloblastoma stem cells, and especially oral cancer stem cells, pancreatic cancer stem cells and brain tumor stem cells.
In medicine, a tumor refers to an abnormal cytopathic effect, which is caused by a reaction of various carcinogenic factors that causes cells in the local body tissues to lose normal growth regulation at the genetic level and results in an abnormal cell proliferation. Those abnormal proliferated cells will aggregate into a mass, and this is called as a “tumor.” “Cancer” is the most common type of tumor. The abnormal proliferated “cancer cells” will not only aggregate into a mass, but also spread and metastasize to other tissues or organs. Therefore, cancer is also known as a malignant tumor. The proliferation and metastasis of cancer cells will cause severe abnormalities of physiological function and is very difficult to cure; therefore, cancer is currently the first cause of death worldwide.
Traditional methods for treating cancer include surgery, chemotherapy and radiation therapy, etc. Cancer, however, cannot be cured completely by surgical excision of the mass because the cancer cells not exactly cut off may continuously grow and result in an exacerbation of the patient's condition. Therefore, surgical excision is not used alone in the therapy for cancer, and is usually combined with other therapeutic methods such as chemotherapy and/or radiation therapy. In chemotherapy, chemical drugs (such as an alkylating agent) are used to kill the cancer cells having a high proliferation rate. However, most chemical drugs used in chemotherapies also act on normal cells, resulting in severe side effects (include vomiting, alopecia, fatigue, bleeding, anemia, etc.) to cancer patients. Radiation therapy (e.g., gamma knife radiosurgery) breaks down the DNA of cancer cells on the principle that rapidly dividing cancer cells are more sensitive to radiation than normal cells. However, when high-energy radiation destroys cancer cells, normal cells may also be radiated simultaneously, resulting in side effects such as a loss of leukocytes, fatigue, insomnia, pain, and poor appetite. Furthermore, chemotherapy and radiation therapy are not effective for a part of cancer patients in the late stages.
Research has shown that most cancer cells do not have the ability to induce a tumor and only few cancer cells have tumorigenicity. Those cancer cells with tumorigenicity have characteristics of stem cells (i.e., have the ability of self-renewal and differentiation), and can continuously grow and differentiate into different kinds or types of tumor cells, and thus, are called as “cancer stem cells (CSCs)” or “tumor stem cells”. Research has also shown that cancer stem cells have the potential to form a tumor and develop into cancer. In particular, cancer stem cells will develop into other kinds of cancer when metastasizing to other tissues or organs of the body. Furthermore, in the tissues of such as leukemia, breast cancer, brain cancer, ovarian cancer, prostate cancer, colon cancer, rectal cancer, or oral cancer, cancer stem cells are more resistant to chemotherapy or radiation therapy than other cells. Such resistance is highly correlated with the recurrence, invasion, and metastasis of the tumor and survival rate of the patient. Thus, if the growth, migration, invasion and/or metastasis of cancer stem cells can be prevented, mitigated or inhibited effectively, the success rate for treating the tumor and cancer and the survival rate of patient can be improved.
Currently, the therapeutic methods (including surgery, chemotherapy and radiation therapy, etc.) for preventing, mitigating or inhibiting the growth, migration, invasion or metastasis of cancer stem cells in clinic are all inefficient. Therefore, there is a necessity and urgency for developing a method or a drug for preventing, mitigating or inhibiting the growth, migration, invasion or metastasis of cancer stem cells effectively to decrease the incidence rate, recurrent rate, and death rate, as well as to improve the cure rate and reduce side effects.
Inventors of the present invention found that BP is effective in inhibiting the expressions of the growth related factors, stemness factors, epithelial-mesenchymal transition (EMT) factors, and gelatinases of cancer stem cells, especially in inhibiting the expressions of Sox-2, Oct4 and EZH2, and thus, can inhibit the growth, migration, invasion and metastasis of cancer stem cells and can be used to provide a medicament, a food product or a food additive for preventing, mitigating and/or inhibiting the growth, migration, invasion and/or metastasis of cancer stem cells.
An objective of the present invention is to provide a use of butylidenephthalide (BP) in the manufacture of a preparation, wherein the preparation is for preventing, mitigating and/or inhibiting the growth, migration, invasion and/or metastasis of cancer stem cells (CSCs). Preferably, the preparation is a medicament, a food product, or a food additive
Another objective of the present invention is to provide a method for preventing, mitigating and/or inhibiting the growth, migration, invasion and/or metastasis of cancer stem cells (CSCs), comprising administering to a subject in need an effective amount of butylidenephthalide (BP).
The detailed technology and preferred embodiments implemented for the present invention are described in the following paragraphs accompanying the appended drawings for people skilled in this field to well appreciate the features of the claimed invention.
The patent application contains at least one drawing executed in color. Copies of this patent document with color drawing(s) will be provided by the Patent and Trademark Office upon request and payment of the necessary fee.
The following will describe some of the embodiments of the present invention in detail. However, without departing from the spirit of the present invention, the present invention may be embodied in various embodiments and should not be limited to the embodiments described in the specification. In addition, unless otherwise indicated herein, the expressions “a,” “an”, “the”, or the like recited in the specification of the present invention (especially in the claims) are intended to include the singular and plural forms. The term “effective amount” or “therapeutically effective amount” used in this specification refers to the amount of compound that can at least partially alleviate the condition that is being treated in a suspected subject when administrated to the subject in need. The term “subject” used in this specification refers to a mammalian, including human or non-human animals.
Inventors of the present invention found that butylidenephthalide (BP) is effective in inhibiting the viability of cancer stem cells, inhibiting the expressions of growth related factors (e.g., EZH2) of cancer stem cells, inhibiting the expressions of the stemness-maintenance markers (e.g., CD133, Sox-2, Oct4) of cancer stem cells, inhibiting the expressions of genes (e.g., AXL) or proteins (Axl, Gas6, MMP-2) related to the proliferation, anti-apoptosis, migration and invasion of cancer stem cells, inhibiting the expressions of proteins related to EMT (epithelial-mesenchymal transition) (e.g., E-cadherin, TGFβ-1 and Slug) of cancer stem cells, and inhibiting the ability of cancer stem cells to migrate to the wound. In some embodiments of the present invention, BP prevented, mitigated and/or inhibited the growth, migration, invasion and/or metastasis of cancer stem cells by inhibiting the expressions of Sox-2, Oct-4 and EZH2.
Therefore, the present invention relates to the use of BP in the manufacture of a preparation, wherein the preparation is for preventing, mitigating and/or inhibiting the growth, migration, invasion and/or metastasis of cancer stem cells.
The preparation of the present invention can be used in any suitable cancer stem cells and the examples of the cancer stem cells include, for example, oral cancer stem cells, nasopharyngeal cancer stem cells, esophageal cancer stem cells, myeloma stem cells, skin cancer stem cells, melanoma stem cells, thyroid cancer stem cells, lymphoma stem cells, leukemia stem cells, breast cancer stem cells, bladder cancer stem cells, ovarian cancer stem cells, cervical cancer stem cells, prostate cancer stem cells, gastric cancer stem cells, liver cancer stem cells, lung cancer stem cells, colon cancer stem cells, rectal cancer stem cells, pancreatic cancer stem cells, gall bladder cancer stem cells, renal cancer stem cells, glioblastoma stem cells, thymic carcinoma stem cells, rhabdomyosarcoma stem cells, brain tumor stem cells and medulloblastoma stem cells. In some embodiments of the present invention, the preparation is used to prevent, mitigate and/or inhibit the growth, migration, invasion and/or metastasis of oral cancer stem cells, pancreatic cancer stem cells and/or brain tumor stem cells.
The preparation in accordance with the present invention can be provided in any suitable form without particular limitations. For example, the preparation can be provided as medicaments, but is not limited thereby. The preparation can also be provided in liquid or solid form as a food product or food additive.
When the preparation according to the present invention is provided as a medicament, the medicament can be prepared in any suitable dosage form depending on the desired administration manner. For example, the medicament can be administered by oral or parenteral (e.g., subcutaneous, intravenous, intramuscular, peritoneal, or nasal) route to a subject in need, but is not limited thereby. Depending on the form and purpose, suitable carriers can be chosen and used to provide the medicament, wherein examples of the suitable carriers include excipients, diluents, auxiliaries, stabilizers, absorbent retarders, disintegrants, hydrotropic agents, emulsifiers, antioxidants, adhesives, binders, tackifiers, dispersants, suspending agents, lubricants, hygroscopic agents, etc.
As a dosage form suitable for oral administration, the medicament provided by the present invention can comprise any pharmaceutically acceptable carrier (e.g., water, saline, dextrose, glycerol, ethanol or its analogs, cellulose, starch, sugar bentonite, or combinations thereof) that will not adversely affect the desired effects of BP. The medicament can be provided in any dosage form suitable for oral administration, such as be provided as a tablet (e.g., dragee), a pill, a capsule, a granule, a pulvis, a fluidextract, a solution, syrup, a suspension, an emulsion, and a tincture, etc.
As for an injection form for subcutaneous, intravenous, intramuscular, or peritoneal administration or a drip form, the medicament provided by the present invention can comprise one or more ingredient(s) such as an isotonic solution, a salt-buffered saline (e.g., phosphate-buffered saline or citrate-buffered saline), a hydrotropic agent, an emulsifier, 5% sugar solution, and other carriers to provide the medicament as an intravenous infusion, an emulsified intravenous infusion, a powder for injection, a suspension for injection, or a powder suspension for injection, etc. Alternatively, the medicament can be prepared as a pre-injection solid. The pre-injection solid can be provided in a form which is soluble in other solutions or suspensions, or in an emulsifiable form. A desired injection is provided by dissolving the pre-injection solid in a solution or a suspension or emulsifying it prior to being administered to a subject in need. In addition, examples of the dosage form for external use which are suitable for nasal or transdermal administration include an emulsion, a cream, gel (e.g., hydrogel), paste (e.g., a dispersion paste, an ointment), a spray, or a solution (e.g., a lotion, a suspension).
Optionally, the medicament provided by the present invention can further comprise a suitable amount of additives, such as a flavoring agent, a toner, or a coloring agent for enhancing the palatability and the visual perception of the medicament, and/or a buffer, a conservative, a preservative, an antibacterial agent, or an antifungal agent for improving the stability and storability of the medicament. In addition, the medicament can optionally further comprise one or more other active ingredients or be used in combination with a medicament comprising one or more other active ingredients, to further enhance the effects of the medicament or to increase the application flexibility and adaptability of the formulation thus provided, as long as the other active ingredient(s) will not adversely affect the desired effects of BP.
Depending on the age, body weight, and health conditions (such as the disease to be treated and its severity) of the subject to be administrated, the medicament provided by the present invention can be applied with various administration frequencies, such as once a day, multiple times a day, or once every few days, etc. For example, when the medicament is applied orally to a subject for preventing, mitigating and/or inhibiting the growth, migration, invasion and/or metastasis of cancer stem cells, the dosage of the medicament is about 30 mg (as BP)/kg-body weight to about 500 mg (as BP)/kg-body weight per day, preferably about 40 mg (as BP)/kg-body weight to about 120 mg (as BP)/kg-body weight per day, and more preferably about 50 mg (as BP)/kg-body weight to about 90 mg (as BP)/kg-body weight per day, wherein the unit “mg/kg-body weight” refers to the dosage required per kg-body weight of the subject. However, for acute patients, the dosage may be optionally increased up to such as several folds or dozen fold, depending on the practical requirements.
Optionally, the medicament of the present invention can be used in combination with surgery, chemotherapy, radiation therapy, antibody therapy, immunotherapy, anti-angiogenesis therapy, phenotype conversion and/or differentiation therapy, to prevent, mitigate and/or inhibit the growth, migration, invasion and/or metastasis of cancer stem cells.
When the preparation according to the present invention is provided as a food additive, the food additive can be in a form that could be conveniently added during the food manufacturing processes, such as in the form of powder, liquid, suspension or granule. When the preparation according to the present invention is provided as a food product, the food product can be such as milk products, processed meat, breads, pasta products, biscuits, troches, juices, teas, sport drinks, nutritious drinks, and the likes, and can be heath food (e.g., nutritional supplements after surgery), but is not limited thereby.
Depending on the age, body weight and healthy conditions of the subject to be administrated, the health food provided by the present invention can be taken in various frequencies, such as once a day, several times a day or once every few days, etc. The amount of BP in the health food provided by the present invention can be adjusted, preferably to the amount that should be taken daily, depending on the specific population. For example, if the recommended daily dosage for a subject is about 50 mg and each serving of the health food contains 25 mg of BP, the subject can take about two servings of the health food per day.
The recommended daily dosages, use standards and use conditions for a specific population (e.g., pregnant woman and diabetic patients), or recommendations for a use in combination with another food or medicament can be indicated on the outer package of the health food of the present invention, and thus, is favorable for user to take the health food by him- or herself safely and securely without the instructions of a doctor, pharmacist, or related executive.
The present invention also provides a method for preventing, mitigating and/or inhibiting the growth, migration, invasion and/or metastasis of cancer stem cells (CSCs), comprising administering to a subject in need an effective amount of butylidenephthalide (BP). In this method, the applied form and suitable dosage of BP and suitable cancer stem cells are all in line with the above description about the preparation of the present invention.
The present invention will be further illustrated in detail with specific examples as follows. However, the following examples are provided only for illustrating the present invention, and the scope of the present invention is not limited thereby. The scope of the present invention is shown in the claims.
(1-1)
To investigate the effect of BP on inhibiting the growth of cancer stem cells, brain CSCsCD133+ or malignant glioma DBTRG cells were treated with different concentrations (0, 25, 50, 62.5, 75 and 100 μg/ml) of BP, different concentrations (0, 25, 125, 250, 500 and 1000 μM) of bis-chloroethylnitrosourea (BCNU, a currently used chemotherapy drug for treating malignant glioma in clinic), or different concentrations (0, 100, 200, 400, 800 and 1600 μM) of temozolomide (TMZ, a currently used chemotherapy drug for treating malignant glioma in clinic) for 24 or 48 hours. Thereafter, a cell viability assay, MTT assay, was utilized to analyze the viabilities of brain CSCsCD133+ and malignant glioma DBTRG cells. The viability of each experimental group was calculated based on the result of the control group, i.e., the group without being treated with BP, BCNU or TMZ. The results are shown in
As shown in
(1-2)
NHOKs (normal human oral keratinocytes) and HNC-TIC (head and neck cancer-derived tumor initiating cell)-like oral stem cells (i.e., ALDH1+CD44+-1 cell line or ALDH1+CD44+-2 cell line) were treated with different concentrations (0, 25, 50 and 100 μg/ml) of BP for 24 hours, and then, an MTT assay was utilized to analyzed the viabilities of NHOKs and HNC-TIC-like oral stem cells (i.e., ALDH1+CD44+-1 cell line and ALDH1+CD44+-2 cell line). The results are shown in
As shown in
It has been known that EZH2 (enhancer of zeste homolog 2) gene is a critical growth related factor of cancer stem cells, and it will affect the growth and growth characteristics of cancer stem cells. Brain CSCsCD133+ was treated with different concentrations (0, 12.5, 25, 50, 62.5 and 75 μg/ml) of BP, and then, proteins were extracted from the cells to conduct Western blotting to determine the expression of EZH2 protein in the BP-treated brain CSCsCD133+. The results are shown in
As shown in
(3-1)
It has been known that CD44, CD133, Sox-2 (sex-determining region Y protein (SRY)-related high-mobility group box 2) and Oct4 (octamerbinding transcription factor 4) proteins all are stemness-maintenance markers of cancer stem cells and participate in the regulation of the self-renewal and differentiation of cancer stem cells. Brain CSCsCD133+ was treated with different concentrations (0, 12.5, 25, 50, 62.5 and 75 μg/ml) of BP for 24 hours, and then, proteins were extracted from the cells to conduct Western blotting to determine the expressions of CD133, Sox-2 and Oct4 proteins in the BP-treated brain CSCsCD133+. The results are shown in
As shown in
(3-2)
ALDH protein is also an important stemness-maintenance marker of cancer stem cells and participates in the regulation of the self-renewal and differentiation of cancer stem cells. HNC-TIC-like oral stem cells (i.e., ALDH1+CD44+-1 cell line or ALDH1+CD44+-2 cell line) were treated with different concentrations (0, 25 and 50 μg/ml) of BP for 24 hours, and then, 1×105 cells obtained from each group were separately suspended in 50 μl of a stem cell detection kit (i.e., ALDEFLUOR array kit, purchased from STEMCELL Technologies Inc., Vancouver, Canada) buffer and the cell suspension of each group was separately added with ALDEFLUOR to a final concentration of 1 μM. Thereafter, a sample of each group was stained by 7-ADD and then analyzed by flow cytometry analysis to determine the ALDH activity of HNC-TIC-like oral stem cells (i.e., ALDH1+CD44+-1 cell line and ALDH1+CD44+-2 cell line). The results are shown in
The above experimental procedure was repeated, but the cell suspension of each group was further added with N,N-diethylaminobenzaldehyde (DEAB, i.e., an inhibitor of ALDH) to a final concentration of 150 μM of DEAB separately. The results are also shown in
As shown in
(4-1)
It has been known that the expression of Axl (i.e., a receptor tyrosine kinase) is related to the ability of cancer stem cells in proliferation, anti-apoptosis, migration and invasion. Brain CSCsCD133+ was treated with different concentrations (0, 12.5, 25, 50, 62.5 and 75 μg/ml) of BP for 24 hours, and then, proteins and total RNA were extracted from the cells to conduct Western blotting and reverse transcriptase-polymerase chain reaction (RT-PCR) to determine the expressions of Axl and Gas6 (i.e., a ligand of Axl) proteins and the expression of Axl gene in the BP-treated brain CSCsCD133+. The results are shown in
As shown in
(4-2)
It has been known that at the start of the invasion of cancer stem cells, the extracellular matrix (ECM) is degraded by matrix metalloproteinases (MMPs). Wherein, the expressions of gelatinases, such as gelatinase-A (i.e., MMP-2) and gelatinase-B (i.e., MMP-9), are highly related to the histopathology of tumor metastasis. Brain CSCsCD133+ was treated with different concentrations (0, 12.5, 25, 50, 62.5 and 75 μg/ml) of BP for 24 hours, and then, proteins were extracted from the cells to conduct Western blotting to determine the expression of MMP-2 protein in the BP-treated brain CSCsCD133+. The results are shown in
As shown in
(4-3)
In this research, the effect of BP on inhibiting the migration and invasion of cancer stem cells was further investigated by a transwell invasion assay system (i.e., Transwell® system, purchased from Corning, UK) with a polycarbonate filter membrane of pore size (purchased from Corning, UK). First, the polycarbonate filter membrane was coated with Matrigel™ (purchased from BD Pharmingen, USA), and then, the coated membrane was placed in the lower chamber of the transwell invasion assay system. Then, the lower chamber was filled with 10% serum-containing medium. On the other hand, HNC-TIC-like oral stem cells (i.e., ALDH1+CD44+-1 cell line or ALDH1+CD44+-2 cell line) were treated with different concentrations (0, 25 and 50 μg/ml) of BP for 24 hours, and then, the treated cells of each group was cultured in the upper chamber which was filled with serum-free medium, at a cell density of 1×105 cells/100 μl for 24 hours. Lastly, the medium of the lower chamber was removed, and the polycarbonate filter membrane in the lower chamber was taken out, fixed with 4% formalin and stained with crystal violet. The invasion cancer cells of each group were counted and photographed over five visual fields of the membrane with the use of a 100-fold magnification under a microscope. The results are shown in
As shown in
(5-1)
In has been known that at the start of the epithelial-mesenchymal transition (EMT) of cancer stem cells, the expression of E-cadherin would reduce and the aggregation force between cancer stem cells would decrease, so that the cancer stem cells would gain great invasion and migration capacity and depart from the primary tumor, and thus, could metastasize. Brain CSCsCD133+ was treated with different concentrations (0, 12.5, 25, 50, 62.5 and 75 μg/ml) of BP for 24 hours, and then, proteins were extracted from the cells to conduct Western blotting to determine the expressions of E-cadherin, TGFβ-1 (with an ability to induce EMT) and Slug (i.e., a member of Snail family transcriptional repressors with a property of promoting the metastasis of cancer cells) proteins in the BP-treated brain CSCsCD133+. The results are shown in
As shown in
(5-2)
In this research, a wound healing assay was used to further investigate the effect of BP on inhibiting the metastasis of cancer stem cells. First, brain CSCsCD133+ was treated with different concentrations (0, 12.5. 25, 50, 62.5 and 75 μg/ml) of BP or different concentrations (0, 25, 50, 100, 200 and 400 μM) of BCNU for 24 hours. At the same time, the phenomenon of brain CSCsCD133+ migrates to the wound was observed and photographed at 0 and 24 hours during the BP treatment or BCNU treatment, respectively. The results are shown in
As shown in
(5-3)
In this research, to further investigate whether the capability of BP in inhibiting the metastasis of cancer stem cells is related to Axl, brain CSCsCD133+ was transfected with pcDNA3.0-Axl plasmid and pcDNA3.0-neo plasmid respectively by using Lipofectmine 2000 transfection reagent. Then, the transfected brain CSCsCD133+ and un-transfected brain CSCsCD133+ were selected by 200 to 600 μg/ml G418 at the same time to obtain brain CSCsCD133+ having pcDNA3.0-Axl plasmid (hereinafter referred to as “pcDNA 3.0-Axl brain CSCsCD133+”) or brain CSCsCD133+ having pcDNA3.0-neo plasmid (hereinafter referred to as “pcDNA3.0-neo brain CSCsCD133+”). Both pcDNA 3.0-Axl brain CSCsCD133+ and pcDNA3.0-neo brain CSCsCD133+ were observed and photographed with the use of a microscope. The results are shown in
As shown in
(6-1)
In this research, a soft agar colony formation assay was used to investigate the effect of BP on inhibiting the tumor initiating activity of cancer stem cells. First, HNC-TIC-like oral stem cells (i.e., ALDH1+CD44+-1 cell line or ALDH1+CD44+-2 cell line) were treated with different concentrations (0, 25 and 50 μg/ml) of BP for 24 hours, and then, the treated cells of each group was separately seeded in the top agar [containing DMEM (Dulbecco's Modified Eagle's Medium medium), 10% (v/v) Fetal Calf Serum (FCS) and 0.3% (w/v) agar] (purchased from Sigma-Aldrich) at an initial cell number of 2×104. On the other hand, a six-well culture dish was coated with the bottom agar [containing DMEM, 10% (v/v) FCS and 0.6% (w/v) agar] (purchased from Sigma-Aldrich), 2 ml for each well. After the bottom agar was solidified, each group of the top agar (containing oral cancer stem cells) was respectively added onto the bottom agar in different wells of the dish, 2 ml for each well. Thereafter, the culture dish was placed in an 37° C. incubator for 4 weeks. Lastly, the bottom agar was stained with 0.005% crystal violet, the number of colonies (with a diameter ≧100 μm) was counted over five fields per well with the use of a microscope, and those fields were photographed. The results are shown in
As shown in
(6-2)
In this research, the effect of BP on inhibiting the tumor initiating activity of cancer stem cells was further investigated by animal experiments. First, 5-6 weeks old BALB/c nu/nu mice (weight 18-22 g) were bred under the same condition for 4 weeks. Then, HNC-TIC-like oral stem cells stably transfected with GFP-tagged constructs were injected (1×104 cells/0.1 mL/mouse) subcutaneously into the axilla of mice. After tumors reached 100 mm3, mice were grouped into one control group and two experimental groups (three groups in total, n=3 per group). Then, one experimental group was injected daily with 100 mg/kg of BP for 6 days and another experimental group was injected daily with 200 mg/kg of BP for 6 days. The control group was injected daily with a vehicle (without BP) for 6 days. Ten days after the injection of BP or vehicle, the length and width were measured every 2 days (22 days in total), and then, the average tumor volume was calculated according to the following Formula 1. The results are shown in
[length×width2]/2 (unit: mm3) Formula 1
As shown in
As shown by the above experimental results, BP is effective in inhibiting the viabilities of cancer stem cells, inhibiting the expressions of growth related factors of cancer stem cells, inhibiting the expressions of the stemness-maintenance markers of cancer stem cells, inhibiting the expressions of the genes/proteins related to the proliferation, anti-apoptosis, migration and invasion of cancer stem cells, inhibiting the expressions of the genes/proteins related to the metastasis of cancer stem cells, and inhibiting the abilities of cancer stem cells to migrate to the wound. In particular, BP is effective in inhibiting the expressions of Sox-2, Oct4 and EZH2, and thus, can be used to prevent, mitigate and/or inhibit the growth, migration, invasion and/or metastasis of cancer stem cells.
Not applicable.
Not applicable.
Number | Date | Country | Kind |
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105117580 | Jun 2016 | TW | national |
This application claims priority to U.S. Provisional Application Ser. No. 62/207,226 filed on Aug. 19, 2015, in the United States Patent and Trademark Office, and to Taiwan Patent Application No. 105117580 filed on Jun. 3, 2016, in the Taiwan Intellectual Property Office, the disclosures of which are incorporated herein in their entirety by reference.
Number | Date | Country | |
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62207226 | Aug 2015 | US |