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Cancer-associated fibroblast regulation of tumor neo-angiogenesis as a therapeutic target in cancer

Adequate blood supply is essential for tumor survival, growth and metastasis. The tumor microenvironment (TME) is dynamic and complex, comprising cancer cells, cancer-associated stromal cells and their extracellular products. The TME serves an important role in tumor progression. Cancer-associated f...

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Detalles Bibliográficos
Autores principales: Wang, Fang-Tao, Sun, Wei, Zhang, Jing-Tao, Fan, Yue-Zu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396119/
https://www.ncbi.nlm.nih.gov/pubmed/30867734
http://dx.doi.org/10.3892/ol.2019.9973
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author Wang, Fang-Tao
Sun, Wei
Zhang, Jing-Tao
Fan, Yue-Zu
author_facet Wang, Fang-Tao
Sun, Wei
Zhang, Jing-Tao
Fan, Yue-Zu
author_sort Wang, Fang-Tao
collection PubMed
description Adequate blood supply is essential for tumor survival, growth and metastasis. The tumor microenvironment (TME) is dynamic and complex, comprising cancer cells, cancer-associated stromal cells and their extracellular products. The TME serves an important role in tumor progression. Cancer-associated fibroblasts (CAFs) are the principal component of stromal cells within the TME, and contribute to tumor neo-angiogenesis by altering the proteome and degradome. The present paper reviews previous studies of the molecular signaling pathways by which CAFs promote tumor neo-angiogenesis and highlights therapeutic response targets. Also discussed are potential strategies for antitumor neo-angiogenesis to improve tumor treatment efficacy.
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spelling pubmed-63961192019-03-13 Cancer-associated fibroblast regulation of tumor neo-angiogenesis as a therapeutic target in cancer Wang, Fang-Tao Sun, Wei Zhang, Jing-Tao Fan, Yue-Zu Oncol Lett Review Adequate blood supply is essential for tumor survival, growth and metastasis. The tumor microenvironment (TME) is dynamic and complex, comprising cancer cells, cancer-associated stromal cells and their extracellular products. The TME serves an important role in tumor progression. Cancer-associated fibroblasts (CAFs) are the principal component of stromal cells within the TME, and contribute to tumor neo-angiogenesis by altering the proteome and degradome. The present paper reviews previous studies of the molecular signaling pathways by which CAFs promote tumor neo-angiogenesis and highlights therapeutic response targets. Also discussed are potential strategies for antitumor neo-angiogenesis to improve tumor treatment efficacy. D.A. Spandidos 2019-03 2019-01-25 /pmc/articles/PMC6396119/ /pubmed/30867734 http://dx.doi.org/10.3892/ol.2019.9973 Text en Copyright: © Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Review
Wang, Fang-Tao
Sun, Wei
Zhang, Jing-Tao
Fan, Yue-Zu
Cancer-associated fibroblast regulation of tumor neo-angiogenesis as a therapeutic target in cancer
title Cancer-associated fibroblast regulation of tumor neo-angiogenesis as a therapeutic target in cancer
title_full Cancer-associated fibroblast regulation of tumor neo-angiogenesis as a therapeutic target in cancer
title_fullStr Cancer-associated fibroblast regulation of tumor neo-angiogenesis as a therapeutic target in cancer
title_full_unstemmed Cancer-associated fibroblast regulation of tumor neo-angiogenesis as a therapeutic target in cancer
title_short Cancer-associated fibroblast regulation of tumor neo-angiogenesis as a therapeutic target in cancer
title_sort cancer-associated fibroblast regulation of tumor neo-angiogenesis as a therapeutic target in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396119/
https://www.ncbi.nlm.nih.gov/pubmed/30867734
http://dx.doi.org/10.3892/ol.2019.9973
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