Emerging Hsp90 Inhibitors: from Discovery to Clinic
Overview
Affiliations
Hsp90 is a chaperone with important roles in maintaining transformation and in elevating the survival and growth potential of cancer cells. Activation of signaling pathways mediated by Hsp90 protein clients is necessary for cell proliferation, regulation of cell cycle progression and apoptosis. Additionally, gain-of-function mutations responsible for transformation often require Hsp90 for the maintenance of their folded, functionally active conformations. These characteristics promise Hsp90 as an important target in cancer therapy and prompt for the identification, development and clinical translation of small molecule inhibitors of the chaperone. This review intends to update the reader on the status of several existing and emerging classes of direct inhibitors of Hsp90 ATPase activity.
General Structural and Functional Features of Molecular Chaperones.
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PMID: 34569020 DOI: 10.1007/978-3-030-78397-6_2.
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PMID: 34070744 PMC: 8197790. DOI: 10.3390/ijms22115859.
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PMID: 32117034 PMC: 7026490. DOI: 10.3389/fneur.2020.00076.
Regulation of CLC-1 chloride channel biosynthesis by FKBP8 and Hsp90β.
Peng Y, Huang J, Wu H, Hsieh H, Wu C, Chen S Sci Rep. 2016; 6:32444.
PMID: 27580824 PMC: 5007535. DOI: 10.1038/srep32444.
Development of Noviomimetics as C-Terminal Hsp90 Inhibitors.
Anyika M, McMullen M, Forsberg L, Dobrowsky R, Blagg B ACS Med Chem Lett. 2016; 7(1):67-71.
PMID: 26819668 PMC: 4716602. DOI: 10.1021/acsmedchemlett.5b00331.