Abstract
Several years ago a hypothesis was proposed that the survival of cancer cells depends 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.
Original language | English |
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Pages (from-to) | 2306-2310 |
Number of pages | 5 |
Journal | Cell Cycle |
Volume | 13 |
Issue number | 14 |
DOIs | |
State | Published - 15 Jul 2014 |
Externally published | Yes |
Keywords
- Chaperone
- Hsp70
- Non-oncogene addiction
- Proteotoxic stress
- Rational drug targeting
All Science Journal Classification (ASJC) codes
- Molecular Biology
- Developmental Biology
- Cell Biology