articleJournal of Biological ChemistryMay 30, 2003HYBRID OA

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

PubMed
Indexed incrossrefdoajpubmed

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

690
total citations
FWCI
11.43
Percentile
100%
References
47
Citations per year

Authors

6

Topics & keywords

Keywords
  • Unfolded protein response
  • Endoplasmic reticulum
  • Cell biology
  • Topoisomerase
  • Programmed cell death
  • Etoposide
  • Camptothecin
  • Apoptosis
UN Sustainable Development Goals
  • Good health and well-being
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