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Proteotoxicity is not the reason for the dependence of cancer cells on the major chaperone Hsp70.
- Source :
-
Cell cycle (Georgetown, Tex.) [Cell Cycle] 2014; Vol. 13 (14), pp. 2306-10. Date of Electronic Publication: 2014 Jun 09. - Publication Year :
- 2014
-
Abstract
- Several years ago a hypothesis was proposed that the survival of cancer cells depend on elevated expression of molecular chaperones because these cells are prone to proteotoxic stress. A critical prediction of this hypothesis is that depletion of chaperones in cancer cells should lead to proteotoxicity. Here, using the major chaperone Hsp70 as example, we demonstrate that its depletion does not trigger proteotoxic stress, thus refuting the model. Accordingly, other functions of chaperones, e.g., their role in cell signaling, might define the requirements for chaperones in cancer cells, which is critical for rational targeting Hsp70 in cancer treatment.
- Subjects :
- Breast Neoplasms genetics
Breast Neoplasms pathology
Down-Regulation
Female
Gene Expression Regulation, Neoplastic
HEK293 Cells
HSP70 Heat-Shock Proteins genetics
HeLa Cells
Heat-Shock Response
Humans
MCF-7 Cells
Protein Refolding
RNA Interference
Signal Transduction
Time Factors
Transfection
Uterine Cervical Neoplasms genetics
Uterine Cervical Neoplasms pathology
Breast Neoplasms metabolism
HSP70 Heat-Shock Proteins metabolism
Uterine Cervical Neoplasms metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1551-4005
- Volume :
- 13
- Issue :
- 14
- Database :
- MEDLINE
- Journal :
- Cell cycle (Georgetown, Tex.)
- Publication Type :
- Academic Journal
- Accession number :
- 24911412
- Full Text :
- https://doi.org/10.4161/cc.29296