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Controlling the unfolded protein response-mediated life and death decisions in cancer
- 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
- Subjects :
- Cell death
Cancer Research
Programmed cell death
Cell Survival
[SDV.CAN]Life Sciences [q-bio]/Cancer
Apoptosis
UPR
Protein Serine-Threonine Kinases
Biology
Endoplasmic Reticulum
Malignant transformation
Adenosine Triphosphate
Neoplasms
Endoribonucleases
medicine
Animals
Homeostasis
Humans
Cell Lineage
Cancer
Oncogene
Endoplasmic reticulum
Endoplasmic Reticulum Stress
medicine.disease
Activating Transcription Factor 6
Cell biology
Cell Transformation, Neoplastic
Cancer cell
Unfolded Protein Response
Unfolded protein response
ER stress
Signal Transduction
Subjects
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