WO2010062143A9 - L1cam의 활성 또는 발현을 억제하는 물질 및 항암제를 포함하는 항암용 조성물 - Google Patents
L1cam의 활성 또는 발현을 억제하는 물질 및 항암제를 포함하는 항암용 조성물 Download PDFInfo
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- C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
Definitions
- the present invention relates to an anticancer composition
- an anticancer composition comprising a substance that inhibits the activity or expression of L1CAM and an anticancer agent, and more particularly, to inhibits the expression of L1CAM-specific anti-L1CAM antibody, L1CAM as a substance that inhibits the activity of L1CAM.
- Oligonucleotide that inhibits the invention of L1CAM as a substance, and a substance selected from cisplatin, gemcitabine, 5-fluorouracil and Taxol as an anticancer agent the two substances may be administered alone
- the present invention relates to an anticancer composition that effectively treats cancer, particularly L1CAM-expressing cancer, by exhibiting a synergistic therapeutic effect.
- L1 cell adhesion molecule is an endogenous membrane glycoprotein belonging to immunoglobulin superfamily cell adhesion molecules (CAMs) that mediate cell-to-cell adhesion at the cell surface.
- CAMs immunoglobulin superfamily cell adhesion molecules
- One of the integral membrane glycoproteins has a molecular weight of 220 kDa.
- L1CAM was originally found in neurons and its function is known as neuron migration, neurite outgrowth and cell migration. L1CAM has been known to be expressed in several normal tissues in addition to neural tissues, and has recently been found in several cancer cells.
- European patent application EP 1 172 654 and US patent application US 2004/0259084 provide for the diagnosis and diagnosis of ovarian cancer or endometrial cancer, provided that L1CAM is a marker for the presence of ovarian cancer, endometrial cancer or the predisposition of such cancer.
- L1CAM protein is a very specific marker of ovarian cancer or endometrial cancer in body fluids or tissues.
- US patent application US 2004/0115206 includes agents that induce cancer cell death such as breast cancer, colorectal cancer, cervical cancer using antibodies that specifically bind to L1CAM, means for using the antibody for cell death, and L1CAM antibodies.
- a modified pharmaceutical composition which inhibits cell growth and induces cell death by contacting the cell with an effective amount of an anti-L1CAM antibody capable of inhibiting cell growth and inducing cell death in cancer cells. It is.
- a monoclonal antibody (A10-A3) was obtained by immunizing mice with a biliary tract cancer cell line, and it was confirmed that the A10-A3 antibody specifically recognized L1CAM. It was confirmed that L1CAM was expressed on the surface of biliary tract cancer cells using -A3 antibody. From the statistical analysis of the relationship between the expression rate and the survival rate of biliary tract cancer patients, the mortality rate of the group with high L1CAM expression rate was higher We confirmed that L1CAM acts as a poor prognositic factor for biliary tract cancer, confirming that it is significantly higher than the low group mortality rate.
- L1CAM may have an excellent diagnostic or therapeutic effect on biliary tract cancer.
- Anticancer drugs are drugs that exhibit cytotoxicity or cytostatic effects on cancer cells by acting on various metabolic pathways of cancer cells, and the anticancer drugs developed so far are metabolic antagonists, Vegetable alkaloids, topoisomerase inhibitors, alkylating agents, anticancer antibiotics, hormones and other drugs can be classified. Anticancer drugs vary in intracellular targets, depending on the drug, blocking the DNA replication, transcription and translation processes of the cell or disrupting the action of proteins important for cell survival. The effects on these intracellular targets are subsequently processed through necrosis or apoptosis. Kills cells. The metabolic pathways in which these anticancer drugs work are not specific to cancer cells but are also the same for normal cells.
- anticancer drugs So far, more than 50 anticancer drugs have been developed, and there are differences in the anticancer agents used depending on the type and characteristics of the cancer, and they are used for cancer treatment alone or in combination with other anticancer therapies.
- the most commonly used anticancer agents include DNA alkylating agents (cyclophosphamide, ifosfamide), metabolic agents (methotrexate, folate inhibitors, 5-fluorouracil ( 5-fluorouracil, pyrimidine inhibitors), microtubule inhibitors (vincristine, vinblastine, paclitaxel), DNA intercalators (doxorubicin, cisplatin ( cisplatin), and hormonal therapies (tamoxifen, flutamide).
- DNA alkylating agents cyclophosphamide, ifosfamide
- metabolic agents metalhotrexate, folate inhibitors, 5-fluorouracil ( 5-fluorouracil, pyrimidine inhibitors), microtubule inhibitors (vincristine
- Cisplatin was developed in 1968 as a cytotoxic anticancer agent and is known to inhibit cell division by binding to double strands of DNA and connecting with neighboring DNA to inhibit the separation of DNA strands. Cisplatin is the most widely used anticancer agent and is particularly used for the treatment of solid cancers such as ovarian cancer, testicular cancer and head and neck cancer. However, its use is limited in cancers that have acquired resistance to cisplatin as an intrinsic or exogenous factor (Andrews, PA and Howell, SB. (1990) Cancer cells; Kelley, sl and Rozencweig, M (1989) Eur. J. Clin. Oncol. 25: 1135-1140; Perez, RP et al. (1990) pharmacol. Ther. 48: 19-27; and Timmer-Bosscha, H. et al. (1992) Br. J. Cancer 66 : 227-238). Therefore, there is a need for treatment through co-administration with inhibitors to induce resistance.
- Gemcitabine (2'-deoxy-2 ', 2'-difluorocytidine) is a nucleoside analogue that is an anticancer agent that inhibits cell proliferation through the synthesis of DNA.
- Bladder cancer, breast cancer, lung cancer, ovarian cancer It is used to treat solid cancers such as biliary tract cancer, and pancreatic cancer.
- Gemcitabine is clinically very effective but its concentration is very limited because of side effects such as anemia, leukocytosis and neutropenia, increased liver efficiency, vomiting, and high fever. Therefore, there is a need to develop a combination therapy that can increase the therapeutic efficacy while reducing the concentration of gemcitabine.
- 5-fluorouracil is a metabolic antagonist with cytotoxicity. It is an anticancer agent used for the treatment of solid cancers such as gastrointestinal cancer, breast cancer, and head and neck cancer, and is widely used in combination with other anticancer agents.
- solid cancers such as gastrointestinal cancer, breast cancer, and head and neck cancer
- the combination of calcium salts of leucovorin and folinic acid is known to be very effective in the treatment of solid cancer (Malet-martino M et al. Clinical studies of three oral prodrugs of 5-fluorouracil (5). -fluorouracil) (Capecitabine, UFT, S-1): A review.Oncologist 2002; 4 (4) 228-323).
- DPD dihydropyrimidine dehydrogenase
- Docetaxel Docetaxel, Taxol
- paclitaxel is an anticancer agent used to treat solid tumors or malignant tumors with high metastasis. Is disclosed.
- the amount of docetaxel used is 60-300 mg / m 2 , which varies from patient to patient, and is usually injected over a period of 3 weeks at a concentration of 60-100 mg / m 2 via intravenous route (Texbook of Medical Oncology, Franco Cavelli). et al., Martin Dunitz Ltd., p.4623 (1997)).
- Many clinical studies have demonstrated the efficacy of docetaxel, particularly in the treatment of breast cancer, and it is generally known that its efficacy can be seen after 1-2 treatments.
- the mechanism of action of docetaxel has been shown to increase the assembly of microtuble and to inhibit the depolymerization of tubulin.
- the inventors of the present invention have been studying active ingredients having an excellent effect as anticancer agents, by using a combination of conventional anticancer agents and substances that inhibit the activity or expression of L1CAM, which can be used as a single agent, can provide a remarkably effective anticancer agent. It confirmed and completed this invention.
- An object of the present invention includes a substance that inhibits the activity or expression of L1CAM and an anticancer agent, and exhibits a synergistic therapeutic effect than when the two substances are administered alone, effectively for the treatment of cancer, especially cancer expressing L1CAM It is to provide a composition.
- an anticancer composition comprising a substance that inhibits the activity or expression of L1CAM and an anticancer agent according to the present invention, by simultaneously, separately or sequentially using a substance that inhibits the activity or expression of L1CAM included therein and an anticancer agent, Compared to each of the pharmacological effects of these substances alone, it has a much stronger and significant cancer cell growth and death effect, thereby treating cancer, especially ovarian cancer, endometrial cancer, cervical cancer, breast cancer, known as L1CAM-expressing carcinoma. It is very useful for various cancers such as colorectal cancer, melanoma, neuroblastoma, biliary tract cancer, lung cancer and pancreatic cancer.
- Figure 1 is a result of analyzing the cell proliferation inhibitory effect after administration of L1CAM-expressing antibody A10-A3 and cisplatin to L1CAM-expressing L1CAM and cisplatin, respectively, or in combination
- B) is a result of analyzing apoptosis induction effect after administration of L1CAM antibody A10-A3 and cisplatin to L1CAM-expressing bile duct cancer cell line (SCK), or in combination, respectively,
- Figure 2 is a group of mice (10 mice each) in combination with mIgG, L1CAM antibody A10-A3, cisplatin, or A10-A3 and cisplatin in a mouse (xenograft) model transplanted with L1CAM expressing cholangiocarcinoma cell line (SCK). ) Shows the growth of cancer,
- Figure 5 (A) is a result of comparing the expression level of mRNA and protein of L1CAM in cell lines that inhibited L1CAM expression using a specific siRNA for L1CAM in the biliary cancer cell line (SCK) expressing L1CAM and control cells. ,
- Figure 5 (B) shows a cell proliferation inhibitory effect by the combined administration of cisplatin in the cell line that inhibited the expression of L1CAM using a specific siRNA for L1CAM in the biliary cancer cell line (SCK) expressing L1CAM and control cells Is,
- FIG. 5 (C) shows the effect of inducing apoptosis by co-administration of cisplatin in a cell line which inhibited L1CAM expression using a specific siRNA for L1CAM in a biliary cancer cell line (SCK) expressing L1CAM and a control cell line. to be.
- SCK biliary cancer cell line
- the present invention relates to a composition for anticancer comprising the following (a) and (b) as an active ingredient simultaneously, separately or sequentially used:
- the composition of the present invention may comprise a substance for inhibiting the activity of L1CAM as (a).
- the activity inhibitor is an anti-L1CAM antibody that specifically recognizes L1CAM known as cancer cell surface antigen or secreted surface antigen.
- Such antibodies include both monoclonal antibodies and chimeric and humanized antibodies thereto, and may include antibodies known in the art, in addition to novel antibodies, which may be prepared by methods well known in the art. Can be.
- the antibodies included in the composition of the present invention can be easily produced by known monoclonal antibody production techniques and known methods for chimeric and humanizing such monoclonal antibodies.
- methods for preparing monoclonal antibodies can be performed by preparing hybridomas using B lymphocytes from immunized animals (Koeher and Milstein, 1976, Nature, 256: 495), or phage display (phage). display) technology, but is not limited thereto.
- the antibody library using phage display technology is a method of expressing an antibody on a phage surface by obtaining an antibody gene from B lymphocytes without producing hybridomas.
- Phage display technology can overcome many of the existing difficulties associated with generating monoclonal antibodies by B-cell immortalization.
- Typical phage display techniques include the steps of: 1) inserting oligonucleotides of random sequence into the gene region corresponding to the coat protein pIII (or pIV) N-terminus of the phage; 2) expressing a fusion protein of a portion of the native coat protein and a polypeptide encoded by the oligonucleotide of the random sequence; 3) processing a receptor material capable of binding to the polypeptide encoded by the oligonucleotide; 4) eluting peptide-phage particles bound to the receptor using low pH or binding competitive molecules; 5) amplifying the eluted phage in the host cell by panning; 6) repeating the method to obtain the desired amount; And 7) determining the sequence of the active peptide from the DNA sequence of the phage clones selected by panning.
- L1CAM-specific anti-L1CAM production method is, for example, by a phage display method that picks out an antibody binding to L1CAM from a human antibody library by panning, or by immunizing mice with L1CAM protein to prepare a library or to prepare a hybridoma. It may be by a method for producing an antibody that binds to L1CAM. More preferably, the antibody is A10-A3, which is an anti-L1CAM antibody described in Korean Patent No. 10-0756051 and / or Korean Patent Laid-Open No. 10-2008-0018149, and such A10-A3 antibody is known from the above-mentioned documents. It can be produced by a method as described in, preferably produced by secretion by accession number KCTC 10909BP.
- anti-L1CAM antibodies include functional antigenic fragments of antibody molecules, as well as complete forms having the full length of two heavy chains and two light chains, as long as they have the property of binding to specifically recognize L1CAM.
- the functional antigenic fragment of an antibody molecule means the fragment which has at least antigen binding function, and includes Fab, F (ab '), F (ab') 2 , Fv, etc.
- the anticancer composition may include a substance that inhibits the expression of L1CAM as (a). Inhibiting the expression of L1CAM by using substances that inhibit the expression of L1CAM in cancer cells expressing L1CAM reduces the effect of L1CAM, which plays a role in the growth and metastasis of cancer cells, thereby enabling cancer treatment.
- the substance that inhibits the expression of L1CAM is selected from the group consisting of siRNA, shRNA and antisense oligonucleotide, more preferably 5'-GCCAATGCCTACATCTACGTT-3 'sequence (SEQ ID NO: 1) SiRNA containing.
- siRNA refers to a small nucleic acid molecule of about 20 nucleotides in size that can mediate RNA interference or gene silencing
- shRNA refers to 5-9 bases of the sense and antisense sequences of the siRNA target sequence.
- Short hairpin RNA short hairpin RNA
- RNAi RNA interference
- the method for preparing siRNA included in the composition of the present invention includes a method of chemically synthesizing siRNA directly (Sui G et al., (2002) Proc Natl Acad Sci USA 99: 5515-5520), a method of synthesizing siRNA using in vitro transcription ( Brummelkamp TR et al., (2002) Science 296: 550-553), but are not limited thereto.
- shRNA overcomes disadvantages such as high cost of biosynthesis of siRNA, short time maintenance of RNA interference effect due to low cell transfection efficiency, and uses adenovirus, lentivirus and plasmid expression vector system from promoter of RNA polymerase III.
- shRNA can be introduced into a cell to express it, and it is widely known that such shRNA is converted into an siRNA having an accurate structure by an siRNA processing enzyme (Dicer or Rnase III) present in the cell to induce silencing of a target gene.
- an siRNA processing enzyme Diicer or Rnase III
- antisense refers to a sequence and subnucleotide sequence of nucleotide bases, wherein the antisense oligomers hybridize to the target sequence in RNA by Watson-Crick base pairing, allowing formation of mRNA and RNA: oligomeric heterodimers, typically within the target sequence. Refers to oligomers with interunit backbones. The oligomer may have exact sequence complementarity or approximate complementarity to the target sequence. These antisense oligomers can alter or process the processing of mRNA, which blocks or inhibits translation of mRNA and produces splice variants of the mRNA. Thus, the antisense oligomers of the invention are antisense oligomers complementary to the mRNA of the L1CAM gene.
- composition of the present invention includes (b) for administering an anticancer agent in combination with (a).
- anticancer agent is a generic term for known drugs used in the treatment of conventional cancers that act on various metabolic pathways of cancer cells and exhibit cytotoxicity or cytostatic effects on cancer cells. Metabolism inhibitors, vegetable alkaloids, topoisomerase inhibitors, alkylating agents, anticancer antibiotics, hormones and other drugs. Substances that inhibit the activity or expression of L1CAM and particularly anticancer agents included in the composition according to the present invention include cisplatins such as cisplatin, carboplatin and heptaplatin, gemcitabine, 5-fluoro Taxols such as 5-urauracil and docetaxel and its derivatives paclitaxel are preferred, and particularly preferred anticancer agents are cisplatin. These anticancer agents can be manufactured by a well-known method, or can use a commercial item.
- the substance that inhibits the activity or expression of the L1CAM and the anticancer agent may be mixed and administered at the same time, but each may be administered separately or simultaneously or serially or separately.
- two active ingredients may be alternately administered, or one may be administered continuously followed by the other.
- the composition should just contain the substance which suppresses the activity or expression of L1CAM, and an anticancer agent as an active ingredient, and may be a drug of any form.
- the mixture containing two active ingredients may be comprised, and may be comprised as a single agent, respectively.
- the combination refers to the formulation of two or more active ingredients in one formulation
- the term single agent refers to the inclusion of one active ingredient in one formulation, wherein the active ingredients are determined according to their pharmacological and pharmacokinetic properties.
- Different formulations may be prepared and combined.
- the therapeutic agent in the case where the two active ingredients are monosaccharides means a medicament used in combination of single agents that can be used singly. If the two active ingredients are single agents, they may be in the form of a kit in which both components are present at once.
- the anticancer composition of the present invention may be administered daily or intermittently, and the number of administrations per day may be administered once or divided into several times. When two active ingredients are each single, the number of administrations may be the same or different.
- the anticancer composition of the present invention can be formulated by a known method alone or with a suitable pharmaceutically acceptable carrier or excipient as described below.
- suitable pharmaceutically acceptable carrier or excipient include oral, injectable or external preparations such as soft capsules, hard capsules, tablets and syrups.
- Pharmaceutically acceptable carriers include any of the standard pharmaceutical carriers used in known formulations such as sterile solutions, tablets, coated tablets and capsules.
- such carriers include polyvinylpyrrolidone, dextrin, starch, milk, sugar, certain types of clays, gelatin, stearic acid, talc, vegetable oils (e.g. cooking oil, cottonseed oil, coconut oil, almond oil, peanut oil).
- Excipients such as oily esters such as neutral fatty acid glycerides, mineral oil, petrolatum, animal fats and oils, and cellulose derivatives (e.g. crystalline cellulose, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, methyl cellulose); Or other known excipients.
- Such carriers may also include antioxidants, wetting agents, viscosity stabilizers, flavoring agents, color additives and other ingredients. Compositions containing such carriers can be formulated by known methods.
- compositions of the present invention may be administered in a pharmaceutically effective amount for the treatment of cancer.
- Typical dosage levels and proportions of (a) and (b) materials can be optimized using standard clinical techniques.
- the present invention relates to a method for treating cancer using the anticancer composition.
- the treatment method of the present invention includes administering the anticancer composition to the human body in a pharmaceutically effective amount.
- the anticancer composition may be administered orally, subcutaneously, intraperitoneally, in pulmonary, and intranasally, and is administered by a suitable method including topical administration if necessary for local treatment.
- Non-oral infusions include intramuscular, intravenous, intraarterial, intraperitoneal or subcutaneous administration.
- Preferred modes of administration are intravenous injection, subcutaneous injection, intradermal injection, intramuscular injection and instillation injection.
- the dosage of the substances may vary depending on various factors, and the route of administration also includes various factors such as the patient's age, duration of administration, weight, severity of the disease, whether the patient is conscious and the type of concomitant drug. It is possible to use various routes of administration orally or parenterally. It is also possible to administer each separately separately or simultaneously, or separately over time.
- the present invention relates to the use of the anticancer composition for the manufacture of a medicament for the treatment of cancer.
- the cancer may be included without limitation the cancer treated by the composition, for example, biliary tract cancer, endometrial cancer, cervical cancer, breast cancer, colon cancer, ovarian cancer, melanoma, neuroblastoma, lung cancer or pancreatic cancer Can be mentioned.
- the manufacture of a medicament for treating cancer can be prepared by well-known or known techniques in the art, as well as the above-mentioned methods.
- the present invention relates to the use of the composition for containing cancer for the treatment of cancer.
- the cancer may be included without limitation the cancer treated by the composition, for example, biliary tract cancer, endometrial cancer, cervical cancer, breast cancer, colon cancer, ovarian cancer, melanoma, neuroblastoma, lung cancer or pancreatic cancer Can be mentioned.
- the inventors of L1CAM to determine whether cancer cell proliferation is more effectively inhibited than when each alone when administered anti-L1CAM antibody and anti-cancer agent to L1CAM-expressing cancer cells
- A10-A3 a monoclonal antibody that inhibits action
- gemcitabine a monoclonal antibody that inhibits action
- 5-fluorouracil a monoclonal antibody that inhibits action
- each of them exhibits a superior synergistic effect than when administered alone to express cancer treatment, especially L1CAM. It is effective against various cancers known as ovarian cancer, endometrial cancer, cervical cancer, breast cancer, colon cancer, melanoma, neuroblastoma, biliary tract cancer, lung cancer and pancreatic cancer.
- All cancer cell lines were cultured in a 37 ° C. incubator with 5% carbon dioxide using the following medium containing 10% fetal bovine serum (Gibco).
- SCK biliary cancer cell line
- SK-OV3 ovarian cancer cell line
- DMEM Well GENE
- the A10-A3 antibody used as anti-L1CAM antibody was prepared by the method disclosed in Korean Patent Laid-Open No. 10-2008-0018149.
- Each cancer cell was counted by 2 x 10 5 cells in 3 ml of medium, cultured in 6 well plates, cisplatin and A10-A3 (10 ⁇ g / ml) alone or in combination, and then the cells were treated at 37 ° C. Incubated for 72 hours in a CO 2 reactor. The cells were recovered and counted the dead and living cells in 0.2% Tryphan Blue solution, and the living cells in the total cells were calculated as percentages. As a result, in the group treated with cisplatin and A10-A3 (10 ⁇ g / ml) alone, it was confirmed that the proliferation of these cancer cells was 30-50% inhibited. The synergistic effect of inhibiting cell proliferation was confirmed (FIG. 1A).
- apoptosis experiments were performed to determine whether apoptosis was induced more effectively when A10-A3 and cisplatin were co-administered to L1CAM.
- This experiment uses the principle that DNA breaks down when cells die.
- Each cancer cell line was counted by 2 x 10 4 cells in 100 ⁇ l of medium and incubated in a 96 well plate, and treated with cisplatin and A10-A3 (10 ⁇ g / ml) alone or in combination. , Incubated for 24 hours. After 24 hours, the medium was removed and washed with PBS buffer, and then the cell lysis solution (RIPA buffer) was reacted at 37 ° C. for 30 minutes.
- RIPA buffer cell lysis solution
- DNA-specific biotin was bound to the lysed cell solution and 20 ⁇ l was transferred to a 96-well plate containing streptavidin, followed by 80 ⁇ l of immunoreagent to confirm absorbance at 405 nm. It was. As a result, when a combination of A10-A3 and cisplatin (cisplatin), it was confirmed that apoptosis was significantly increased compared to the group treated alone (Fig. 1 (B)).
- Nude mouse Balb / c nu / nu was purchased from SLC (Japan) via central laboratory animal history. Age and weight ranged from 6-8 weeks of age and 18-22g, and were purified for 1 week at the Korea Research Institute of Bioscience and Biotechnology. Subsequently, 1 ⁇ 10 7 cells of SCK cells were implanted into 40 subcutaneous cells. After one week, when tumor volume reached 100-200 mm 3 , randomly divided into four groups of 10 animals. A10-A3 was treated three times a week at a concentration of 10 mg / kg, and cisplatin was treated twice a week at a concentration of 3 mg / kg.
- the control group was treated with the same amount of mIgG instead of A10-A3, and the same amount of saline instead of cisplatin.
- the mass and tumor weight of nude mice were measured three times a week.
- the proliferative inhibitory effect was about 30%, whereas the co-administered group showed a clear inhibitory effect of more than 70% ( 2).
- Example 2 In the same manner as in Example 2, when A10-A3 and gemcitabine were administered in combination, it was analyzed whether cell proliferation was inhibited more effectively than when administered alone. As a result, in the group treated with gemcitabine and A10-A3 (10 ⁇ g / ml) alone, the proliferation of these cancer cells was 20-25% (biliary cancer, SCK) or 20-40% (ovarian cancer, SK-OV3). It was confirmed that the inhibition, when combined treatment was confirmed a synergistic effect of suppressing the cell growth of about 40-60% (Fig. 3 (A)).
- Example 2 In the same manner as in Example 2, when A10-A3 and 5-fluorouracil were administered in combination, the cell proliferation was more effectively inhibited than when administered alone. As a result, the proliferation of these cancer cells in the group treated with 5-fluorouracil and A10-A3 (10 ⁇ g / ml) alone was 20-40% (biliary cancer, SCK) or 20-30%. (Ovarian cancer, SK-OV3) It was confirmed that the inhibition, when combined treatment was confirmed a synergistic effect of suppressing the cell growth of about 40-50% (Fig. 4).
- SiRNA specific for L1CAM (5'-GCCAATGCCTACATCTACGTT-3 ', SEQ ID NO: 1) and nonspecific siRNA (5'-CAGTCGCGTTTGCGACTGG-3', SEQ ID NO: 2) to knock down L1CAM expression in biliary cancer cell line SCK )
- 1ml Trizol reagent (Invitrogen) was treated at room temperature for 5 minutes.
- the solution was treated with 0.2ml chloroform and shaken vigorously about 15 times, followed by reaction at room temperature for 3 minutes. After centrifugation at 4 ° C.
- siRNA specific for L1CAM (5'-GCCAATGCCTACATCTACGTT-3 ', SEQ ID NO: 1) and nonspecific siRNA (5'-CAGTCGCGTTTGCGACTGG-3', SEQ ID NO: 2) to knock down L1CAM expression in biliary cancer cell line SCK )
- siRNA specific for L1CAM 5'-GCCAATGCCTACATCTACGTT-3 ', SEQ ID NO: 1
- nonspecific siRNA 5'-CAGTCGCGTTTGCGACTGG-3', SEQ ID NO: 2
- PBST PBS + 0.1% Tween 20
- the reacted nitrocellulose membrane was reacted for 2 hours by adding a known anti-L1CAM antibody A10-A3 as the primary antibody. After washing 5 times with the PBST buffer solution, and reacted with an HRP (horseradish peroxidase) conjugate (1: 5000 Sigma) of anti-mouse IgG for 1 hour. After washing 5 times with PBST buffer, it was developed with ECL detection reagent (Amersham biosciences). As a result, it was confirmed that the total protein expression amount of L1CAM was reduced in the group treated with the specific siRNA compared to the control treated with non-specific siRNA for L1CAM (Fig. 5 (A) below).
- Example 6-3 Analysis of cell proliferation inhibitory effect and induction of apoptosis by co-administration of siRNA and anticancer agent that inhibit L1CAM expression
- siRNA for L1CAM (5'-GCCAATGCCTACATCTACGTT-3 ', SEQ ID NO: 1) and nonspecific siRNA (5'-CAGTCGCGTTTGCGACTGG-3') to knock down expression of L1CAM in biliary cancer cell line SCK expressing L1CAM , SEQ ID NO: 2) were each transduced and incubated for 72 hours. Thereafter, the cell proliferation experiment and the apoptosis experiment were performed by the method described in ⁇ Example 2>.
- an anticancer composition comprising a substance that inhibits the activity or expression of L1CAM and an anticancer agent according to the present invention, by simultaneously, separately or sequentially using a substance that inhibits the activity or expression of L1CAM included therein and an anticancer agent, Compared to each of the pharmacological effects of these substances alone, it has a much stronger and significant cancer cell growth and death effect, thereby treating cancer, especially ovarian cancer, endometrial cancer, cervical cancer, breast cancer, known as L1CAM-expressing carcinoma. It is very useful for various cancers such as colorectal cancer, melanoma, neuroblastoma, biliary tract cancer, lung cancer and pancreatic cancer.
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Abstract
Description
Claims (13)
- 하기의 (a) 및 (b)를 동시에, 별도로 또는 순차적으로 병용하기 위해 유효성분으로 포함하는 항암용 조성물:(a) L1CAM의 활성 또는 발현을 억제하는 물질; 및(b) 항암제이때, 상기 L1CAM의 활성을 억제하는 물질은 L1CAM 특이적인 항-L1CAM 항체, 그의 항원성 결합 단편, 및 항-L1CAM 항체 또는 그 항원성 결합 단편의 변이체로 이루어진 군에서 선택되는 것이고, L1CAM의 발현을 억제하는 물질은 L1CAM의 발현을 억제하는 올리고 뉴클레오티드이며,상기 항암제는 시스플라틴(cisplatin), 젬시타빈(gemcitabine), 5-플루오로우라실(5-fluorouracil), 도세탁셀 및 파클리탁셀에서 선택되는 것을 특징으로 한다.
- 제1항에 있어서, L1CAM의 발현을 억제하는 올리고 뉴클레오티드는 L1CAM을 암호화하는 유전자에 대한 안티센스 올리고뉴클레오티드, siRNA 및 shRNA로 이루어진 군에서 선택되는 것인 조성물.
- 제1항에 있어서, 상기 항-L1CAM 항체가 수탁번호 KCTC 10909BP의 하이브리도마에 의해 분비되는 A10-A3 항체인 조성물.
- 제2항에 있어서, 상기 siRNA는 서열번호 1로 정의되는 서열로 구성되는 것인 조성물.
- 제1항 내지 제4항 중 어느 한 항에 있어서, 상기 항암제는 시스플라틴인 조성물.
- 제1항에 있어서, 암세포의 성장을 억제하거나 암세포를 사멸시키는 것을 특징으로 하는 조성물.
- 제1항에 있어서, 상기 암은 담도암, 자궁내막암, 자궁경부암, 유방암, 대장암, 난소암, 흑색종, 신경아세포종, 폐암 및 췌장암으로 이루어진 군에서 선택되는 것인 조성물.
- 제1항에 있어서, 상기 항암용 조성물은 상기 (a) 및 (b)를 각각 포함하는 독립한 단제의 형태로 제형화 된 것임을 특징으로 하는 조성물.
- 제1항의 항암용 조성물을 투여하는 단계를 포함하는 암의 치료 방법.
- 제9항에 있어서, 상기 암은 담도암, 자궁내막암, 자궁경부암, 유방암, 대장암, 난소암, 흑색종, 신경아세포종, 폐암 및 췌장암으로 이루어진 군에서 선택되는 것인 방법.
- 암 치료용 의약을 제조하기 위한 제1항의 조성물의 용도.
- 제11항에 있어서, 상기 암은 담도암, 자궁내막암, 자궁경부암, 유방암, 대장암, 난소암, 흑색종, 신경아세포종, 폐암 및 췌장암으로 이루어진 군에서 선택되는 것인 용도.
- 담도암, 자궁내막암, 자궁경부암, 유방암, 대장암, 난소암, 흑색종, 신경아세포종, 폐암 또는 췌장암의 치료를 위한 제1항의 조성물의 용도.
Priority Applications (6)
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CA2750147A CA2750147A1 (en) | 2008-11-27 | 2009-11-27 | Anticancer composition comprising antitumor agent and substance having inhibitory effects on l1cam activity and expression |
AU2009320542A AU2009320542A1 (en) | 2008-11-27 | 2009-11-27 | Anticancer composition comprising antitumor agent and substance having inhibitory effects on L1CAM activity and expression |
US13/131,445 US20110293600A1 (en) | 2008-11-27 | 2009-11-27 | Anticancer Composition Comprising Antitumor Agent and Substance Having Inhibitory Effects on L1CAM Activity and Expression |
CN2009801545949A CN102325547A (zh) | 2008-11-27 | 2009-11-27 | 含有抗癌剂和对l1cam的活性和表达具有抑制作用的物质的抗癌组合物 |
JP2011538553A JP2012509935A (ja) | 2008-11-27 | 2009-11-27 | L1camの活性または発現を抑制する物質および抗癌剤を含む抗癌用組成物 |
EP09829350A EP2357003A4 (en) | 2008-11-27 | 2009-11-27 | ANTICANCER COMPOSITION COMPRISING ANTITUMOR SUBSTANCE AND AGENT AND HAVING INHIBITORY EFFECTS ON L1CAM ACTIVITY AND EXPRESSION |
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KR10-2008-0118921 | 2008-11-27 | ||
KR1020080118921A KR20100060351A (ko) | 2008-11-27 | 2008-11-27 | L1cam의 활성 또는 발현을 억제하는 물질 및 항암제를포함하는 항암용 조성물 |
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EP (1) | EP2357003A4 (ko) |
JP (1) | JP2012509935A (ko) |
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CN (1) | CN102325547A (ko) |
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WO2011004379A1 (en) * | 2009-07-10 | 2011-01-13 | Tel Hashomer Medical Research Infrastructure And Services Ltd. | Compositions and methods for treating cancer |
KR101271964B1 (ko) * | 2010-07-08 | 2013-06-07 | 강원대학교산학협력단 | 담낭암 치료용 약제학적 조성물 및 이를 이용한 담낭암의 성장, 전이 억제 및 치료 방법 |
AU2014323491B2 (en) * | 2013-09-18 | 2021-01-14 | Memorial Sloan-Kettering Cancer Center | Inhibiting cancer metastasis |
KR20230170142A (ko) | 2016-08-02 | 2023-12-18 | 메모리얼 슬로안 케터링 캔서 센터 | 전이성 암의 치료 및 전이성 질환에 대한 모델 시스템 |
WO2018124851A1 (ko) * | 2016-12-30 | 2018-07-05 | 강원대학교 산학협력단 | L1cam 단백질에 특이적으로 결합하는 항체; 및 피리미딘 유사체 및/또는 플라틴계 항암제를 포함하는 암의 예방 또는 치료용 약학적 조성물 |
WO2024088283A1 (zh) * | 2022-10-26 | 2024-05-02 | 同润生物医药(上海)有限公司 | 人源化的l1cam抗体药物偶联物 |
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FR2601675B1 (fr) | 1986-07-17 | 1988-09-23 | Rhone Poulenc Sante | Derives du taxol, leur preparation et les compositions pharmaceutiques qui les contiennent |
MX9102128A (es) | 1990-11-23 | 1992-07-08 | Rhone Poulenc Rorer Sa | Derivados de taxano,procedimiento para su preparacion y composicion farmaceutica que los contiene |
ES2296586T3 (es) | 2000-07-10 | 2008-05-01 | Deutsches Krebsforschungszentrum Stiftung Des Offentlichen Rechts | Metodo de diagnostico basado en la deteccion de la molecula de adhesion l1 para tumores de ovario y el endometrio. |
US20040115206A1 (en) | 2002-10-24 | 2004-06-17 | Thomas Primiano | Antibody-mediated induction of tumor cell death |
KR20070084868A (ko) | 2006-02-22 | 2007-08-27 | 삼성전자주식회사 | 무선 수신장치에서 자가 보상방법 |
KR100756051B1 (ko) | 2006-04-03 | 2007-09-07 | 한국생명공학연구원 | L1cam 단백질에 대한 새로운 단일클론항체, 이를분비하는 하이브리도마 및 이의 제조방법 |
CA2661669C (en) * | 2006-08-23 | 2017-02-14 | Korea Research Institute Of Bioscience And Biotechnology | A pharmaceutical composition for treating cholangiocarcinoma, a method for inhibiting growth or invasion of cholangiocarcinoma and a method for treating cholangniocarcinoma |
WO2008046529A1 (en) * | 2006-10-16 | 2008-04-24 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Treatment of chemotherapy- or radiotherapy-resistant tumors using an l1 interfering molecule |
WO2008046459A1 (en) * | 2006-10-16 | 2008-04-24 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Treatment of chemotherapy- or radiotherapy-resistant tumors using an l1 interfering molecule |
EP2170956B1 (en) * | 2007-06-15 | 2014-10-22 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Treatment of tumors using specific anti-l1 antibody |
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- 2009-11-27 JP JP2011538553A patent/JP2012509935A/ja not_active Withdrawn
- 2009-11-27 CN CN2009801545949A patent/CN102325547A/zh active Pending
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CN102325547A (zh) | 2012-01-18 |
AU2009320542A1 (en) | 2011-06-30 |
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JP2012509935A (ja) | 2012-04-26 |
US20110293600A1 (en) | 2011-12-01 |
CA2750147A1 (en) | 2010-06-03 |
WO2010062143A2 (ko) | 2010-06-03 |
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