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HMGB1: A Promising Therapeutic Target for Prostate Cancer

High mobility group box 1 (HMGB1) was originally discovered as a chromatin-binding protein several decades ago. It is now increasingly evident that HMGB1 plays a major role in several disease conditions such as atherosclerosis, diabetes, arthritis, sepsis, and cancer. It is intriguing how deregulati...

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Autores principales: Gnanasekar, Munirathinam, Kalyanasundaram, Ramaswamy, Zheng, Guoxing, Chen, Aoshuang, Bosland, Maarten C., Kajdacsy-Balla, André
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3666291/
https://www.ncbi.nlm.nih.gov/pubmed/23766911
http://dx.doi.org/10.1155/2013/157103
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author Gnanasekar, Munirathinam
Kalyanasundaram, Ramaswamy
Zheng, Guoxing
Chen, Aoshuang
Bosland, Maarten C.
Kajdacsy-Balla, André
author_facet Gnanasekar, Munirathinam
Kalyanasundaram, Ramaswamy
Zheng, Guoxing
Chen, Aoshuang
Bosland, Maarten C.
Kajdacsy-Balla, André
author_sort Gnanasekar, Munirathinam
collection PubMed
description High mobility group box 1 (HMGB1) was originally discovered as a chromatin-binding protein several decades ago. It is now increasingly evident that HMGB1 plays a major role in several disease conditions such as atherosclerosis, diabetes, arthritis, sepsis, and cancer. It is intriguing how deregulation of HMGB1 can result in a myriad of disease conditions. Interestingly, HMGB1 is involved in cell proliferation, angiogenesis, and metastasis during cancer progression. Furthermore, HMGB1 has been demonstrated to exert intracellular and extracellular functions, activating key oncogenic signaling pathways. This paper focuses on the role of HMGB1 in prostate cancer development and highlights the potential of HMGB1 to serve as a key target for prostate cancer treatment.
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spelling pubmed-36662912013-06-13 HMGB1: A Promising Therapeutic Target for Prostate Cancer Gnanasekar, Munirathinam Kalyanasundaram, Ramaswamy Zheng, Guoxing Chen, Aoshuang Bosland, Maarten C. Kajdacsy-Balla, André Prostate Cancer Review Article High mobility group box 1 (HMGB1) was originally discovered as a chromatin-binding protein several decades ago. It is now increasingly evident that HMGB1 plays a major role in several disease conditions such as atherosclerosis, diabetes, arthritis, sepsis, and cancer. It is intriguing how deregulation of HMGB1 can result in a myriad of disease conditions. Interestingly, HMGB1 is involved in cell proliferation, angiogenesis, and metastasis during cancer progression. Furthermore, HMGB1 has been demonstrated to exert intracellular and extracellular functions, activating key oncogenic signaling pathways. This paper focuses on the role of HMGB1 in prostate cancer development and highlights the potential of HMGB1 to serve as a key target for prostate cancer treatment. Hindawi Publishing Corporation 2013 2013-05-12 /pmc/articles/PMC3666291/ /pubmed/23766911 http://dx.doi.org/10.1155/2013/157103 Text en Copyright © 2013 Munirathinam Gnanasekar et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Gnanasekar, Munirathinam
Kalyanasundaram, Ramaswamy
Zheng, Guoxing
Chen, Aoshuang
Bosland, Maarten C.
Kajdacsy-Balla, André
HMGB1: A Promising Therapeutic Target for Prostate Cancer
title HMGB1: A Promising Therapeutic Target for Prostate Cancer
title_full HMGB1: A Promising Therapeutic Target for Prostate Cancer
title_fullStr HMGB1: A Promising Therapeutic Target for Prostate Cancer
title_full_unstemmed HMGB1: A Promising Therapeutic Target for Prostate Cancer
title_short HMGB1: A Promising Therapeutic Target for Prostate Cancer
title_sort hmgb1: a promising therapeutic target for prostate cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3666291/
https://www.ncbi.nlm.nih.gov/pubmed/23766911
http://dx.doi.org/10.1155/2013/157103
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