Back to Search Start Over

Controlling the unfolded protein response-mediated life and death decisions in cancer

Authors :
Eoghan P. McGrath
Katarzyna Mnich
Sandra Healy
Marion Maurel
Eric Chevet
Afshin Samali
Physiopathologie du cancer du foie
Université Bordeaux Segalen - Bordeaux 2-Institut National de la Santé et de la Recherche Médicale (INSERM)
Oncogenesis Stress Signaling (OSS)
Université de Rennes 1 (UR1)
Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-CRLCC Eugène Marquis (CRLCC)
06/RFP/BIC002, Science Foundation Ireland
Ligue Contre le Cancer
IAP 7/32, Interuniversity Attraction Poles
Institut National du Cancer
Université de Rennes (UR)-CRLCC Eugène Marquis (CRLCC)
Source :
Seminars in Cancer Biology, Seminars in Cancer Biology, Elsevier, 2015, 33, pp.57-66. ⟨10.1016/j.semcancer.2015.03.003⟩, Seminars in Cancer Biology, 2015, 33, pp.57-66. ⟨10.1016/j.semcancer.2015.03.003⟩
Publication Year :
2015
Publisher :
Elsevier BV, 2015.

Abstract

International audience; Cancer cells are exposed to intrinsic (oncogene) or extrinsic (microenvironmental) challenges, leading to activation of stress response pathways. The unfolded protein response (UPR) is the cellular response to endoplasmic reticulum (ER) stress and plays a pivotal role in tumor development. Depending on ER stress intensity and duration, the UPR is either pro-survival to preserve ER homeostasis or pro-death if the stress cannot be resolved. On one hand, the adaptive arm of the UPR is essential for cancer cells to survive the harsh conditions they are facing, and on the other hand, cancer cells have evolved mechanisms to bypass ER stress-induced cell death, thereby conferring them with a selective advantage for malignant transformation. Therefore, the mechanisms involved in the balance between survival and death outcomes of the UPR may be exploited as therapeutic tools to treat cancer

Details

ISSN :
1044579X and 10963650
Volume :
33
Database :
OpenAIRE
Journal :
Seminars in Cancer Biology
Accession number :
edsair.doi.dedup.....c0e3fece4def2f94b59bfe7037ded167
Full Text :
https://doi.org/10.1016/j.semcancer.2015.03.003