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- W1997590798 endingPage "1097" @default.
- W1997590798 startingPage "1065" @default.
- W1997590798 abstract "Heat shock proteins (Hsps) represent a diverse group of chaperones that play a vital role in the protection of cells against numerous environmental stresses. Although our understanding of chaperone biology has deepened over the last decade, the atypical extracellular functions of Hsps have remained somewhat enigmatic and comparatively understudied. The heat shock protein 90 (Hsp90) chaperone is a prototypic model for an Hsp family member exhibiting a duality of intracellular and extracellular functions. Intracellular Hsp90 is best known as a master regulator of protein folding. Cancers are particularly adept at exploiting this function of Hsp90, providing the impetus for the robust clinical development of small molecule Hsp90 inhibitors. However, in addition to its maintenance of protein homeostasis, Hsp90 has also been identified as an extracellular protein. Although early reports ascribed immunoregulatory functions to extracellular Hsp90 (eHsp90), recent studies have illuminated expanded functions for eHsp90 in wound healing and cancer. While the intended physiological role of eHsp90 remains enigmatic, its evolutionarily conserved functions in wound healing are easily co-opted during malignancy, a pathology sharing many properties of wounded tissue. This review will highlight the emerging functions of eHsp90 and shed light on its seemingly dichotomous roles as a benevolent facilitator of wound healing and as a sinister effector of tumor progression." @default.
- W1997590798 created "2016-06-24" @default.
- W1997590798 creator A5051319033 @default.
- W1997590798 creator A5078053919 @default.
- W1997590798 creator A5082870360 @default.
- W1997590798 date "2014-05-06" @default.
- W1997590798 modified "2023-10-03" @default.
- W1997590798 title "The Double-Edged Sword: Conserved Functions of Extracellular Hsp90 in Wound Healing and Cancer" @default.
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