Sirolimus and Metformin Synergistically Inhibits Colon Cancer In Vitro and In Vivo.
10.3346/jkms.2017.32.9.1385
- Author:
Nadiar MUSSIN
1
;
Seung Cheol OH
;
Kwang Woong LEE
;
Min Young PARK
;
Sooin SEO
;
Nam Joon YI
;
Hyeyoung KIM
;
Kyung Chul YOON
;
Sung Woo AHN
;
Hyo Sin KIM
;
Suk Kyun HONG
;
Dong Kyu OH
;
Kyung Suk SUH
Author Information
1. Department of Surgery, Seoul National University College of Medicine, Seoul, Korea. kwleegs@gmail.com
- Publication Type:Original Article
- Keywords:
Liver Transplantation;
Immunosuppression;
Colonic Neoplasms;
Metformin
- MeSH:
Animals;
Apoptosis;
Blotting, Western;
Cell Line;
Cell Survival;
Colon*;
Colonic Neoplasms*;
Cyclosporine;
Immunosuppression;
Immunosuppressive Agents;
In Vitro Techniques*;
Liver Transplantation;
Metformin*;
Mice;
Models, Animal;
Sirolimus*;
Tacrolimus;
Tumor Burden
- From:Journal of Korean Medical Science
2017;32(9):1385-1395
- CountryRepublic of Korea
- Language:English
-
Abstract:
We estimated the effect of various immunosuppressants (ISs) and metformin (M) to provide theoretical background of optimal therapeutic strategy for de novo colon cancer after liver transplantation (LT). Three colon cancer cell lines (HT29, SW620, and HCT116) were used in in vitro studies. HT29 was also used in BALB/c-nude mice animal models. Following groups were used in both in vitro and in vivo studies: sirolimus (S), tacrolimus (T), cyclosporin A (CsA), M, metformin/sirolimus (Met/S), metformin/tacrolimus (Met/T), and metformin/cyclosporin A (Met/CsA). 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was performed and western blot analyses were performed for mTOR pathway proteins, apoptosis proteins, and epithelial-mesenchymal-transition (EMT) proteins. Tumor volume was measured for 4 weeks after inoculation. MTT-assay revealed significant cell viability inhibition in all 3 colon cancer cell lines in groups of S, M, and Met/S. Of note, group Met/S showed synergistic effect compare to M or S group. Western blot analysis showed significant low levels of all investigated proteins in groups of S and Met/S in both in vitro and in vivo experiment. Tumor growth was significantly inhibited only in the Met/S group. Combination of Met and S showed the most potent inhibition in all colon cancer cell lines. This finding might have application for de novo colon cancer.
