Combination method for treating cancer by targeting immunoglobulin superfamily member 1 (IGSF1) and mesenchymal-epithelial transition factor (MET)
The present invention relates to a biomarker for predicting susceptibility to an MET inhibitor, and a use thereof, and more specifically, the present invention provides a method for predicting susceptibility to the MET inhibitor. According to the present invention, the present invention has an excellent effect of predicting susceptibility to the MET inhibitor for stomach cancer or lung cancer, and thus the present invention may be usefully employed for treating stomach cancer or lung cancer.
1. A method for treating gastric cancer cells or lung cancer cells, wherein said cells have been identified as having expression of the human immunoglobulin superfamily member 1 (IGSF1) gene and wherein said cells have been identified as having hepatocyte growth factor (HGF)-independent MET activation, the method comprising co-administering (a) an agent targeted to IGSF1 for inhibiting the expression of the IGSF1 gene or the expression or activity of its protein; and (b) an agent targeted to MET.
2. The method of claim 1 , wherein the agent targeted to MET is a selective small molecule MET kinase inhibitor.
3. The method of claim 1 , wherein the agent targeted to IGSF1 comprises at least one selected from the group consisting of small interfering RNA (siRNA) and short hairpin RNA (shRNA).
4. The method of claim 1 , wherein the agent targeted to IGSF1 is selected from the group consisting of IGSF1 siRNA comprising the nucleotide sequence of SEQ ID NO:3, IGSF1 siRNA comprising the nucleotide sequence of SEQ ID NO:4, and IGSF1 shRNA comprising the nucleotide sequence of SEQ ID NO:6,
wherein the agent targeted to MET is selected from the group consisting of MET siRNA comprising the nucleotide sequence of SEQ ID NO:5, and MET shRNA comprising the nucleotide sequence of SEQ ID NO: 7.
5. The method of claim 1 , wherein the agent targeted to MET comprises an inhibitor for inhibiting the expression of MET gene or the expression or activity of its protein as an active ingredient.
6. A method for treating gastric cancer cells or lung cancer cells in a patient, the method comprising:
obtaining or having obtained a biological sample from the patient;
detecting or having detected the presence or absence of expression of at least the human immunoglobulin superfamily member 1 (IGSF1) gene in the biological sample;
identifying or having identified whether MET is activated in a hepatocyte growth factor (HGF)-independent manner or -dependent manner in the biological sample; and if the IGSF1 gene is expressed and MET is activated in an HGF-independent manner, then co-administering to said patient a therapeutically effective amount of an agent targeted to IGSF1 and an agent targeted to MET.
7. The method of claim 6 , wherein the agent targeted to MET is a selective small molecule MET kinase inhibitor.
8. The method of claim 6 , wherein the agent targeted to IGSF1 comprises at least one selected from the group consisting of small interfering RNA (siRNA) and short hairpin RNA (shRNA).
9. The method of claim 6 , wherein the agent targeted to IGSF1 is selected from the group consisting of IGSF1 siRNA comprising the nucleotide sequence of SEQ ID NO:3, IGSF1 siRNA comprising the nucleotide sequence of SEQ ID NO:4, and IGSF1 shRNA comprising the nucleotide sequence of SEQ ID NO:6, wherein the agent targeted to MET is selected from the group consisting of MET siRNA comprising the nucleotide sequence of SEQ ID NO:5, and MET shRNA comprising the nucleotide sequence of SEQ ID NO: 7.
10. The method of claim 6 , wherein the agent targeted to MET comprises an inhibitor for inhibiting the expression of MET gene or the expression or activity of its protein as an active ingredient.
11. A method for treating gastric cancer cells or lung cancer cells in a patient, the method comprising:
identifying the patient as having expression of an immunoglobulin superfamily member 1 (IGSF1) gene and having MET activated in an HGF-independent manner, and
co-administering to said patient a therapeutically effective amount of an agent targeted to IGSF1 and an agent targeted to MET.
12. The method of claim 11 , wherein the agent targeted to MET is a selective small molecule MET kinase inhibitor.
13. The method of claim 11 , wherein the agent targeted to IGSF1 comprises at least one selected from the group consisting of small interfering RNA (siRNA) and short hairpin RNA (shRNA).
14. The method of claim 11 , wherein the agent targeted to IGSF1 is selected from the group consisting of IGSF1 siRNA comprising the nucleotide sequence of SEQ ID NO:3, IGSF1 siRNA comprising the nucleotide sequence of SEQ ID NO:4, and IGSF1 shRNA comprising the nucleotide sequence of SEQ ID NO:6, wherein the agent targeted to MET is selected from the group consisting of MET siRNA comprising the nucleotide sequence of SEQ ID NO:5, and MET shRNA comprising the nucleotide sequence of SEQ ID NO: 7.
15. The method of claim 11 , wherein the agent targeted to MET comprises an inhibitor for inhibiting the expression of MET gene or the expression or activity of its protein as an active ingredient.