| Literature DB >> 28454341 |
Rong Zhang1, Yingting Liu1, Kahina Hammache1, Liangqiang He1, Bo Zhu1, Wei Cheng1, Zi-Chun Hua1,2.
Abstract
Pancreatic cancer has one of the poorest patient outcomes and is highly resistant to chemotherapy. Identifying the molecular mechanisms involved in drug resistance is critical in the development of novel strategies to treat pancreatic cancer. The results of the present study demonstrate that Fas-associated death domain protein (FADD), a classical adaptor protein mediating apoptotic stimuli-induced cell death, protects pancreatic cancer cells from drug-induced apoptosis. In contrast to its classical apoptotic roles, it was observed that FADD is required for pancreatic cancer cell proliferation and that it is overexpressed to varying degrees in various types of pancreatic cancer cell. This leads to differing levels of drug resistance in pancreatic cancer cells, where drug resistance is positively correlated with FADD expression. Notably, the results of the present study demonstrate that FADD protects pancreatic cancer cells from drug-induced apoptosis, while RNA interference of FADD sensitizes drug-resistant cells to Adriamycin®-mediated apoptosis. The results of the present study reveal unexpected roles for FADD in pancreatic cancer cell proliferation and drug resistance.Entities:
Keywords: Adriamycin®; Fas-associated death domain protein; apoptosis; cell cycle; pancreatic cancer
Year: 2017 PMID: 28454341 PMCID: PMC5403491 DOI: 10.3892/ol.2017.5636
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967