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Angiogenesis Inhibition in Prostate Cancer: Current Uses and Future Promises

Angiogenesis has been well recognized as a fundamental part of a multistep process in the evolution of cancer progression, invasion, and metastasis. Strategies for inhibiting angiogenesis have been one of the most robust fields of cancer investigation, focusing on the vascular endothelial growth fac...

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Detalles Bibliográficos
Autores principales: Aragon-Ching, Jeanny B., Madan, Ravi A., Dahut, William L.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821752/
https://www.ncbi.nlm.nih.gov/pubmed/20169138
http://dx.doi.org/10.1155/2010/361836
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author Aragon-Ching, Jeanny B.
Madan, Ravi A.
Dahut, William L.
author_facet Aragon-Ching, Jeanny B.
Madan, Ravi A.
Dahut, William L.
author_sort Aragon-Ching, Jeanny B.
collection PubMed
description Angiogenesis has been well recognized as a fundamental part of a multistep process in the evolution of cancer progression, invasion, and metastasis. Strategies for inhibiting angiogenesis have been one of the most robust fields of cancer investigation, focusing on the vascular endothelial growth factor (VEGF) family and its receptors. There are numerous regulatory drug approvals to date for the use of these agents in treating a variety of solid tumors. While therapeutic efficacy has been established, challenges remain with regards to overcoming resistance and assessing response to antiangiogenic therapies. Prostate cancer is the most common noncutaneous malignancy among American men and angiogenesis plays a role in disease progression. The use of antiangiogenesis agents in prostate cancer has been promising and is hereby explored.
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spelling pubmed-28217522010-02-18 Angiogenesis Inhibition in Prostate Cancer: Current Uses and Future Promises Aragon-Ching, Jeanny B. Madan, Ravi A. Dahut, William L. J Oncol Review Article Angiogenesis has been well recognized as a fundamental part of a multistep process in the evolution of cancer progression, invasion, and metastasis. Strategies for inhibiting angiogenesis have been one of the most robust fields of cancer investigation, focusing on the vascular endothelial growth factor (VEGF) family and its receptors. There are numerous regulatory drug approvals to date for the use of these agents in treating a variety of solid tumors. While therapeutic efficacy has been established, challenges remain with regards to overcoming resistance and assessing response to antiangiogenic therapies. Prostate cancer is the most common noncutaneous malignancy among American men and angiogenesis plays a role in disease progression. The use of antiangiogenesis agents in prostate cancer has been promising and is hereby explored. Hindawi Publishing Corporation 2010 2010-02-11 /pmc/articles/PMC2821752/ /pubmed/20169138 http://dx.doi.org/10.1155/2010/361836 Text en Copyright © 2010 Jeanny B. Aragon-Ching 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
Aragon-Ching, Jeanny B.
Madan, Ravi A.
Dahut, William L.
Angiogenesis Inhibition in Prostate Cancer: Current Uses and Future Promises
title Angiogenesis Inhibition in Prostate Cancer: Current Uses and Future Promises
title_full Angiogenesis Inhibition in Prostate Cancer: Current Uses and Future Promises
title_fullStr Angiogenesis Inhibition in Prostate Cancer: Current Uses and Future Promises
title_full_unstemmed Angiogenesis Inhibition in Prostate Cancer: Current Uses and Future Promises
title_short Angiogenesis Inhibition in Prostate Cancer: Current Uses and Future Promises
title_sort angiogenesis inhibition in prostate cancer: current uses and future promises
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821752/
https://www.ncbi.nlm.nih.gov/pubmed/20169138
http://dx.doi.org/10.1155/2010/361836
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