Advances in Anticancer Agents in Medicinal Chemistry

Volume: 1

Indexed in: Book Citation Index, Science Edition, EBSCO, Ulrich's Periodicals Directory

Advances in Anticancer Agents in Medicinal Chemistry is an exciting eBook series comprising a selection of updated articles previously published in the peer-reviewed journal Anti-Cancer Agents in ...
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Recent Advances in Hsp90 Inhibitors as Antitumor Agents

Pp. 107-183 (77)

Samir Messaoudi, Jean F. Peyrat, Jean D. Brion and Mouâd Alami


One promising therapeutic strategy for treating cancer is to specifically target signal transduction pathways that have a key role in oncogenic transformation and malignant progression. Hsp90 is an emerging therapeutic target of interest for the treatment of cancer. It is responsible for modulating cellular response to stress by maintaining the function of numerous signaling proteins - known as ‘client proteins’ - that are associated with cancer cell survival and proliferation. Many cancers result from specific mutations in, or aberrant expression of, these client proteins. Small molecule Hsp90 inhibitors bind to the ATP binding pocket, inhibit chaperone function and could potentially result in cytostasis or cell death. Consequently, many client proteins are targeted for degradation via the ubiquitin-proteasome pathway including receptor and non receptor kinases (Erb-B2, epidermal growth factor receptor, and Src family kinases), serine/threonine kinases (c-Raf-1 and Cdk4), steroid hormone receptors (androgen and estrogen), and apoptosis regulators such as mutant p53. Inhibition of Hsp90 function Hsp90 has also proven effective in kiling cancer cells that have developed resistance to targeted therapies such as kinase inhibitors.

This review is intended to update recent developments in new Hsp90 inhibitors as antitumors agents, the design, biological evaluation and their clinical trials studies.


Cancer, heat shock protein 90 (Hsp90), co-chaperone, client proteins, antitumor agents, NTD-Hsp90 inhibitors, CTD-Hsp90 inhibitors, apoptosis, proteasome.


Univ Paris-Sud, CNRS, BioCIS-UMR 8076, Laboratoire de Chimie Thérapeutique, Faculté de Pharmacie, IFR 141, 5 rue J.-B. Clément, Châtenay- Malabry, F-92296, France