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Progesterone receptor chaperone complex-based high-throughput screening assay: Identification of capsaicin as an inhibitor of the Hsp90 machine

  • Chaitanya A. Patwardhan
    ,
  • Eyad Alfa
    ,
  • Su Lu
    ,
  • Ahmed Chadli(corresponding author)
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Hsp90 and its co-chaperones are known to be important for cancer cell survival. The N-terminal inhibitors of Hsp90 that are in ongoing clinical trials as antitumor agents have unfortunately shown disappointing efficacies in the clinic. Thus, novel inhibitors of the Hsp90 machine with a different mechanism of action are urgently needed. We report here the development of a novel high-throughput screening assay platform to identify small-molecule inhibitors of Hsp90 and its co-chaperones. This assay quantitatively measures the ability of Hsp90 and its co-chaperones to refold/protect the progesterone receptor, a physiological client of Hsp90, in a 96-well plate format. We screened the National Institutes of Health clinical collection drug library and identified capsaicin as a hit molecule. Capsaicin is a Food and Drug Administration-approved drug for topical use in pain management. Cell survival assays showed that capsaicin selectively kills cancer cells and destabilizes several Hsp90 client proteins. Thus, our data may explain the seemingly pleotropic effect of capsaicin.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 223-229 (7 pages)

Journal (Volume, Issue Number)

Journal of Biomolecular Screening (Volume 20, Issue 2)

Publication milestones

  • Published - 02/24/2015

Publication status

Published - 02/24/2015

ISSN

1087-0571

Publication IDs

  • Scopus: 84921523318
  • PubMed: 25184514

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
0.42
SciVal
Author count
4
SciVal
citations
7
SciVal
Paper percentile
61
Fractional count
1
Fractional count
0.25
Fractional count
3
Fractional count
0.75
Fractional count
1
Fractional count
1

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Citation count
13
Captures
18

Funding Details

The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by NIH R01 grant GM102443-01 for Ahmed Chadli.
FundersFunding number
NIH
-
NIGMS
R01GM102443