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Heat Shock Protein 90 and Role of Its Chemical Inhibitors in Treatment of Hematologic Malignancies

Heat shock protein 90 (Hsp90) is a conserved and constitutively expressed molecular chaperone and it has been shown to stabilize oncoproteins and facilitate cancer development. Hsp90 has been considered as a therapeutic target for cancers and three classes of Hsp90 inhibitors have been developed: (1...

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Autores principales: Ho, Ngoc, Li, Adam, Li, Shaoguang, Zhang, Haojian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763672/
https://www.ncbi.nlm.nih.gov/pubmed/24280675
http://dx.doi.org/10.3390/ph5080779
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author Ho, Ngoc
Li, Adam
Li, Shaoguang
Zhang, Haojian
author_facet Ho, Ngoc
Li, Adam
Li, Shaoguang
Zhang, Haojian
author_sort Ho, Ngoc
collection PubMed
description Heat shock protein 90 (Hsp90) is a conserved and constitutively expressed molecular chaperone and it has been shown to stabilize oncoproteins and facilitate cancer development. Hsp90 has been considered as a therapeutic target for cancers and three classes of Hsp90 inhibitors have been developed: (1) benzoquinone ansamycin and its derivatives, (2) radicicol and its derivates, and (3) small synthetic inhibitors. The roles of these inhibitors in cancer treatment have been studied in laboratories and clinical trials, and some encouraging results have been obtained. Interestingly, targeting of Hsp90 has been shown to be effective in inhibition of cancer stem cells responsible for leukemia initiation and progression, providing a strategy for finding a cure. Because cancer stem cells are well defined in some human leukemias, we will focus on hematologic malignancies in this review.
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spelling pubmed-37636722013-11-14 Heat Shock Protein 90 and Role of Its Chemical Inhibitors in Treatment of Hematologic Malignancies Ho, Ngoc Li, Adam Li, Shaoguang Zhang, Haojian Pharmaceuticals (Basel) Review Heat shock protein 90 (Hsp90) is a conserved and constitutively expressed molecular chaperone and it has been shown to stabilize oncoproteins and facilitate cancer development. Hsp90 has been considered as a therapeutic target for cancers and three classes of Hsp90 inhibitors have been developed: (1) benzoquinone ansamycin and its derivatives, (2) radicicol and its derivates, and (3) small synthetic inhibitors. The roles of these inhibitors in cancer treatment have been studied in laboratories and clinical trials, and some encouraging results have been obtained. Interestingly, targeting of Hsp90 has been shown to be effective in inhibition of cancer stem cells responsible for leukemia initiation and progression, providing a strategy for finding a cure. Because cancer stem cells are well defined in some human leukemias, we will focus on hematologic malignancies in this review. MDPI 2012-07-25 /pmc/articles/PMC3763672/ /pubmed/24280675 http://dx.doi.org/10.3390/ph5080779 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Ho, Ngoc
Li, Adam
Li, Shaoguang
Zhang, Haojian
Heat Shock Protein 90 and Role of Its Chemical Inhibitors in Treatment of Hematologic Malignancies
title Heat Shock Protein 90 and Role of Its Chemical Inhibitors in Treatment of Hematologic Malignancies
title_full Heat Shock Protein 90 and Role of Its Chemical Inhibitors in Treatment of Hematologic Malignancies
title_fullStr Heat Shock Protein 90 and Role of Its Chemical Inhibitors in Treatment of Hematologic Malignancies
title_full_unstemmed Heat Shock Protein 90 and Role of Its Chemical Inhibitors in Treatment of Hematologic Malignancies
title_short Heat Shock Protein 90 and Role of Its Chemical Inhibitors in Treatment of Hematologic Malignancies
title_sort heat shock protein 90 and role of its chemical inhibitors in treatment of hematologic malignancies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763672/
https://www.ncbi.nlm.nih.gov/pubmed/24280675
http://dx.doi.org/10.3390/ph5080779
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