Autophagy induced by ionizing radiation promotes cell death over survival in human colorectal cancer cells
Creators
- 1. Institut für Physiologie, Universität Duisburg-Essen, Hufelandstraße 55, Essen, D45147 (Germany)
Description
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.
Additional details
Identifiers
- DOI
- 10.1016/j.yexcr.2018.11.004;
- PII
- S0014482718304610;
Publishing Information
- Journal Title
- Experimental Cell Research
- Journal Volume
- 374
- Journal Issue
- 1
- Journal Page Range
- p. 29-37
- ISSN
- 0014-4827
- CODEN
- ECREAL
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 55042541
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ANOXIA; APOPTOSIS; CARCINOMAS; CELL CYCLE; COLONY FORMATION; GLUTAMINE; INHIBITION; IONIZING RADIATIONS; PROTEINS; RADIOSENSITIVITY; RADIOTHERAPY; SURVIVAL CURVES; TUMOR CELLS
- Descriptors DEC
- AMIDES; AMINO ACIDS; ANIMAL CELLS; CARBOXYLIC ACIDS; DISEASES; MEDICINE; NEOPLASMS; NUCLEAR MEDICINE; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; RADIATIONS; RADIOLOGY; SENSITIVITY; THERAPY
Optional Information
- Copyright
- Copyright (c) 2018 The Authors. Published by Elsevier Inc.