| Literature DB >> 30412717 |
Fabian Classen1, Philip Kranz1, Helena Riffkin1, Mosche Pompsch1, Alexandra Wolf1, Kirsten Göpelt1, Melanie Baumann1, Jennifer Baumann1, Ulf Brockmeier1, Eric Metzen2.
Abstract
Autophagy is commonly described as a cell survival mechanism and has been implicated in chemo- and radioresistance of cancer cells. Whether ionizing radiation induced autophagy triggers tumor cell survival or cell death still remains unclear. In this study the autophagy related proteins Beclin1 and ATG7 were tested as potential targets to sensitize colorectal carcinoma cells to ionizing radiation under normoxic, hypoxic and starvation conditions. Colony formation, apoptosis and cell cycle analysis revealed that knockdown of Beclin1 or ATG7 does not enhance radiosensitivity in HCT-116 cells. Furthermore, ATG7 knockdown led to an increased survival fraction under oxygen and glutamine starvation, indicating that ionizing radiation indeed induces autophagy which, however, leads to cell death finally. These results highlight that inhibition of autophagic pathways does not generally increase therapy success but may also lead to an unfavorable outcome especially under amino acid and oxygen restriction.Entities:
Keywords: Atg7; Autophagy; Beclin1; Glutamine starvation; Hypoxia
Year: 2018 PMID: 30412717 DOI: 10.1016/j.yexcr.2018.11.004
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905