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Heat Shock Proteins and Ovarian Cancer: Important Roles and Therapeutic Opportunities

Ovarian cancer is a serious cause of death in gynecological oncology. Delayed diagnosis and poor survival rates associated with late stages of the disease are major obstacles against treatment efforts. Heat shock proteins (HSPs) are stress responsive molecules known to be crucial in many cancer type...

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Detalles Bibliográficos
Autores principales: Hoter, Abdullah, Naim, Hassan Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769485/
https://www.ncbi.nlm.nih.gov/pubmed/31540420
http://dx.doi.org/10.3390/cancers11091389
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author Hoter, Abdullah
Naim, Hassan Y.
author_facet Hoter, Abdullah
Naim, Hassan Y.
author_sort Hoter, Abdullah
collection PubMed
description Ovarian cancer is a serious cause of death in gynecological oncology. Delayed diagnosis and poor survival rates associated with late stages of the disease are major obstacles against treatment efforts. Heat shock proteins (HSPs) are stress responsive molecules known to be crucial in many cancer types including ovarian cancer. Clusterin (CLU), a unique chaperone protein with analogous oncogenic criteria to HSPs, has also been proven to confer resistance to anti-cancer drugs. Indeed, these chaperone molecules have been implicated in diagnosis, prognosis, metastasis and aggressiveness of various cancers. However, relative to other cancers, there is limited body of knowledge about the molecular roles of these chaperones in ovarian cancer. In the current review, we shed light on the diverse roles of HSPs as well as related chaperone proteins like CLU in the pathogenesis of ovarian cancer and elucidate their potential as effective drug targets.
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spelling pubmed-67694852019-10-30 Heat Shock Proteins and Ovarian Cancer: Important Roles and Therapeutic Opportunities Hoter, Abdullah Naim, Hassan Y. Cancers (Basel) Review Ovarian cancer is a serious cause of death in gynecological oncology. Delayed diagnosis and poor survival rates associated with late stages of the disease are major obstacles against treatment efforts. Heat shock proteins (HSPs) are stress responsive molecules known to be crucial in many cancer types including ovarian cancer. Clusterin (CLU), a unique chaperone protein with analogous oncogenic criteria to HSPs, has also been proven to confer resistance to anti-cancer drugs. Indeed, these chaperone molecules have been implicated in diagnosis, prognosis, metastasis and aggressiveness of various cancers. However, relative to other cancers, there is limited body of knowledge about the molecular roles of these chaperones in ovarian cancer. In the current review, we shed light on the diverse roles of HSPs as well as related chaperone proteins like CLU in the pathogenesis of ovarian cancer and elucidate their potential as effective drug targets. MDPI 2019-09-18 /pmc/articles/PMC6769485/ /pubmed/31540420 http://dx.doi.org/10.3390/cancers11091389 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hoter, Abdullah
Naim, Hassan Y.
Heat Shock Proteins and Ovarian Cancer: Important Roles and Therapeutic Opportunities
title Heat Shock Proteins and Ovarian Cancer: Important Roles and Therapeutic Opportunities
title_full Heat Shock Proteins and Ovarian Cancer: Important Roles and Therapeutic Opportunities
title_fullStr Heat Shock Proteins and Ovarian Cancer: Important Roles and Therapeutic Opportunities
title_full_unstemmed Heat Shock Proteins and Ovarian Cancer: Important Roles and Therapeutic Opportunities
title_short Heat Shock Proteins and Ovarian Cancer: Important Roles and Therapeutic Opportunities
title_sort heat shock proteins and ovarian cancer: important roles and therapeutic opportunities
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769485/
https://www.ncbi.nlm.nih.gov/pubmed/31540420
http://dx.doi.org/10.3390/cancers11091389
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