Endoplasmic Reticulum Chaperone Protein GRP78 Protects Cells from Apoptosis Induced by Topoisomerase Inhibitors
University of Southern California · USC Norris Comprehensive Cancer Center · +3 more institutions
Abstract
A large number of correlative studies have established that the activation of the unfolded protein response (UPR) alters the cell's sensitivity to chemotherapeutic agents. Although the induction of the glucose-regulated proteins (GRPs) is commonly used as an indicator for the UPR, the direct role of the GRPs in conferring resistance to DNA damaging agents has not been proven. We report here that without the use of endoplasmic reticulum (ER) stress inducers, specific overexpression of GRP78 results in reduced apoptosis and higher colony survival when challenged with topoisomerase II inhibitors, etoposide and doxorubicin, and topoisomerase I inhibitor, camptothecin. While investigating the mechanism for the…
Citation impact
- FWCI
- 11.43
- Percentile
- 100%
- References
- 47
Authors
6- RKRamachandra K. ReddyCorresponding
University of Southern California, USC Norris Comprehensive Cancer Center
- CMChanghui Mao
University of Southern California
- PBPeter Baumeister
University of Southern California
- RCRichard C. Austin
McMaster University Medical Centre
- RJRandal J. Kaufman
Howard Hughes Medical Institute, University of Michigan
Topics & keywords
- Unfolded protein response
- Endoplasmic reticulum
- Cell biology
- Topoisomerase
- Programmed cell death
- Etoposide
- Camptothecin
- Apoptosis
- Good health and well-being