Author/Authors :
Mottaghi-Dastjerdi, Negar tehran university of medical sciences tums - School of Pharmacy, Pharmaceutical Biotechnology Research Center - Department of Pharmaceutical Biotechnology, تهران, ايران , Mottaghi-Dastjerdi, Negar mazandaran university of medical sciences - School of Pharmacy, Pharmaceutical Sciences Research Center, ايران , Soltany-Rezaee-Rad, Mohammad tehran university of medical sciences tums - School of Pharmacy, Pharmaceutical Biotechnology Research Center - Department of Pharmaceutical Biotechnology, تهران, ايران , Soltany-Rezaee-Rad, Mohammad mazandaran university of medical sciences - School of Pharmacy, Pharmaceutical Sciences Research Center, ايران , Sepehrizadeh, Zargham tehran university of medical sciences tums - School of Pharmacy, Pharmaceutical Biotechnology Research Center - Department of Pharmaceutical Biotechnology, تهران, ايران , Roshandel, Gholamreza golestan university of medical sciences - Golestan Research Center of Gastroenterology and Hepatology, ايران , Ebrahimifard, Farzaneh shahid beheshti university of medical sciences - School of Medicine - Department of General Surgery, تهران, ايران , Setayesh, Neda tehran university of medical sciences tums - School of Pharmacy, Pharmaceutical Biotechnology Research Center - Department of Pharmaceutical Biotechnology, تهران, ايران
Abstract :
Background: In cancer cells, apoptosis is an important mechanism that influences the outcome of chemotherapy and the development of chemoresistance. To find the genes involved in chemoresistance and the development of gastric cancer, we used the suppression subtractive hybridization method to identify the genes that are overexpressed in gastric cancer tissues compared to normal gastric tissues. Results: In the suppression subtractive hybridization library we constructed, the most highly overexpressed genes were humanin isoforms. Humanin is a recently identified endogenous peptide that has anti-apoptotic activity and has been selected for further study due to its potential role in the chemoresistance of gastric cancer. Upregulation of humanin isoforms was also observed in clinical samples by using quantitative real-time PCR. Among the studied isoforms, humanin isoform 3, with an expression level of 4.166 ± 1.44 fold, was the most overexpressed isoform in GC. Conclusions: The overexpression of humanin in gastric cancer suggests a role for chemoresistance and provides new insight into the biology of gastric cancer. We propose that humanin isoforms are novel targets for combating chemoresistance in gastric cancer.
Keywords :
Apoptosis , Chemoresistance , Gastric cancer , Suppression subtractive hybridization , Humanin