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Int. J. Mol. Sci. 2017, 18(9), 1978;

Targeting Heat Shock Proteins in Cancer: A Promising Therapeutic Approach

Department of Medicine, Division of Hematology Oncology, UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA 15213, USA
Author to whom correspondence should be addressed.
Received: 17 August 2017 / Revised: 1 September 2017 / Accepted: 5 September 2017 / Published: 15 September 2017
(This article belongs to the Special Issue Molecular Chaperones)
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Heat shock proteins (HSPs) are a large family of chaperones that are involved in protein folding and maturation of a variety of “client” proteins protecting them from degradation, oxidative stress, hypoxia, and thermal stress. Hence, they are significant regulators of cellular proliferation, differentiation and strongly implicated in the molecular orchestration of cancer development and progression as many of their clients are well established oncoproteins in multiple tumor types. Interestingly, tumor cells are more HSP chaperonage-dependent than normal cells for proliferation and survival because the oncoproteins in cancer cells are often misfolded and require augmented chaperonage activity for correction. This led to the development of several inhibitors of HSP90 and other HSPs that have shown promise both preclinically and clinically in the treatment of cancer. In this article, we comprehensively review the roles of some of the important HSPs in cancer, and how targeting them could be efficacious, especially when traditional cancer therapies fail. View Full-Text
Keywords: heat shock proteins (HSPs); HSP90; HSP70; HSP90 inhibitors; oncogenes; cancer heat shock proteins (HSPs); HSP90; HSP70; HSP90 inhibitors; oncogenes; cancer

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Chatterjee, S.; Burns, T.F. Targeting Heat Shock Proteins in Cancer: A Promising Therapeutic Approach. Int. J. Mol. Sci. 2017, 18, 1978.

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