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Resistin facilitates VEGF-A-dependent angiogenesis by inhibiting miR-16-5p in human chondrosarcoma cells

Resistin is an adipokine that is associated with obesity, inflammation, and various cancers. Chondrosarcomas are primary malignant bone tumors that have a poor prognosis. VEGF-A is a critical angiogenic factor that is known to promote angiogenesis and metastasis in chondrosarcoma. It is unknown as t...

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Autores principales: Chen, Shiou-Sheng, Tang, Chih-Hsin, Chie, Meng-Ju, Tsai, Chun-Hao, Fong, Yi-Chin, Lu, Yung-Chang, Chen, Wei-Cheng, Lai, Cheng-Ta, Wei, Chuan-Yen, Tai, Huai-Ching, Chou, Wen-Yi, Wang, Shih-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328541/
https://www.ncbi.nlm.nih.gov/pubmed/30631040
http://dx.doi.org/10.1038/s41419-018-1241-2
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author Chen, Shiou-Sheng
Tang, Chih-Hsin
Chie, Meng-Ju
Tsai, Chun-Hao
Fong, Yi-Chin
Lu, Yung-Chang
Chen, Wei-Cheng
Lai, Cheng-Ta
Wei, Chuan-Yen
Tai, Huai-Ching
Chou, Wen-Yi
Wang, Shih-Wei
author_facet Chen, Shiou-Sheng
Tang, Chih-Hsin
Chie, Meng-Ju
Tsai, Chun-Hao
Fong, Yi-Chin
Lu, Yung-Chang
Chen, Wei-Cheng
Lai, Cheng-Ta
Wei, Chuan-Yen
Tai, Huai-Ching
Chou, Wen-Yi
Wang, Shih-Wei
author_sort Chen, Shiou-Sheng
collection PubMed
description Resistin is an adipokine that is associated with obesity, inflammation, and various cancers. Chondrosarcomas are primary malignant bone tumors that have a poor prognosis. VEGF-A is a critical angiogenic factor that is known to promote angiogenesis and metastasis in chondrosarcoma. It is unknown as to whether resistin affects human chondrosarcoma angiogenesis. In this study, we show how resistin promotes VEGF-A expression and subsequently induces angiogenesis of endothelial progenitor cells (EPCs). Resistin treatment activated the phosphatidylinositol-3-kinase (PI3K) and Akt signaling pathways, while PI3K and Akt inhibitors or siRNA diminished resistin-induced VEGF-A expression. In vitro and in vivo studies revealed the downregulation of micro RNA (miR)-16-5p in resistin-induced VEGF-A expression and EPCs angiogenesis. We also found a positive correlation between resistin and VEGF-A expression, and a negative correlation between resistin and VEGF-A with miR-16-5p in chondrosarcoma patients. These findings reveal that resistin facilitates VEGF-A expression and angiogenesis through the inhibition of miR-16-5p expression via PI3K/Akt signaling cascades. Resistin may be a promising target in chondrosarcoma angiogenesis.
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spelling pubmed-63285412019-01-11 Resistin facilitates VEGF-A-dependent angiogenesis by inhibiting miR-16-5p in human chondrosarcoma cells Chen, Shiou-Sheng Tang, Chih-Hsin Chie, Meng-Ju Tsai, Chun-Hao Fong, Yi-Chin Lu, Yung-Chang Chen, Wei-Cheng Lai, Cheng-Ta Wei, Chuan-Yen Tai, Huai-Ching Chou, Wen-Yi Wang, Shih-Wei Cell Death Dis Article Resistin is an adipokine that is associated with obesity, inflammation, and various cancers. Chondrosarcomas are primary malignant bone tumors that have a poor prognosis. VEGF-A is a critical angiogenic factor that is known to promote angiogenesis and metastasis in chondrosarcoma. It is unknown as to whether resistin affects human chondrosarcoma angiogenesis. In this study, we show how resistin promotes VEGF-A expression and subsequently induces angiogenesis of endothelial progenitor cells (EPCs). Resistin treatment activated the phosphatidylinositol-3-kinase (PI3K) and Akt signaling pathways, while PI3K and Akt inhibitors or siRNA diminished resistin-induced VEGF-A expression. In vitro and in vivo studies revealed the downregulation of micro RNA (miR)-16-5p in resistin-induced VEGF-A expression and EPCs angiogenesis. We also found a positive correlation between resistin and VEGF-A expression, and a negative correlation between resistin and VEGF-A with miR-16-5p in chondrosarcoma patients. These findings reveal that resistin facilitates VEGF-A expression and angiogenesis through the inhibition of miR-16-5p expression via PI3K/Akt signaling cascades. Resistin may be a promising target in chondrosarcoma angiogenesis. Nature Publishing Group UK 2019-01-10 /pmc/articles/PMC6328541/ /pubmed/30631040 http://dx.doi.org/10.1038/s41419-018-1241-2 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chen, Shiou-Sheng
Tang, Chih-Hsin
Chie, Meng-Ju
Tsai, Chun-Hao
Fong, Yi-Chin
Lu, Yung-Chang
Chen, Wei-Cheng
Lai, Cheng-Ta
Wei, Chuan-Yen
Tai, Huai-Ching
Chou, Wen-Yi
Wang, Shih-Wei
Resistin facilitates VEGF-A-dependent angiogenesis by inhibiting miR-16-5p in human chondrosarcoma cells
title Resistin facilitates VEGF-A-dependent angiogenesis by inhibiting miR-16-5p in human chondrosarcoma cells
title_full Resistin facilitates VEGF-A-dependent angiogenesis by inhibiting miR-16-5p in human chondrosarcoma cells
title_fullStr Resistin facilitates VEGF-A-dependent angiogenesis by inhibiting miR-16-5p in human chondrosarcoma cells
title_full_unstemmed Resistin facilitates VEGF-A-dependent angiogenesis by inhibiting miR-16-5p in human chondrosarcoma cells
title_short Resistin facilitates VEGF-A-dependent angiogenesis by inhibiting miR-16-5p in human chondrosarcoma cells
title_sort resistin facilitates vegf-a-dependent angiogenesis by inhibiting mir-16-5p in human chondrosarcoma cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328541/
https://www.ncbi.nlm.nih.gov/pubmed/30631040
http://dx.doi.org/10.1038/s41419-018-1241-2
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