4.7 Article

Amphiregulin enhances VEGF-A production in human chondrosarcoma cells and promotes angiogenesis by inhibiting miR-206 via FAK/c-Src/PKCδ pathway

期刊

CANCER LETTERS
卷 385, 期 -, 页码 261-270

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2016.10.010

关键词

Amphiregulin; VEGF-A; Angiogenesis; miR-206

类别

资金

  1. Ministry of Science and Technology of Taiwan [NSC 102-2632-B-039-001-MY3, MOST 103-2628-B-039-002-MY3]
  2. China Medical University [CMU103-AISA-03]

向作者/读者索取更多资源

Chondrosarcoma is the second most common primary malignancy of bone after myeloma and osteosarcoma. Chondrosarcoma development may be linked to angiogenesis, which is principally elicited by vascular endothelial growth factor-A (VEGF-A). The expression of VEGF-A has been recognized as a prognostic marker in angiogenesis. Amphiregulin (AR), an epidermal growth factor receptor ligand, promotes tumor proliferation, metastasis and angiogenesis. However, the role of AR in VEGF-A expression and angiogenesis in human chondrosarcoma remains largely unknown. This current study shows that AR promoted VEGF-A production and induced angiogenesis of human endothelial progenitor cells. Moreover, AR-enhanced VEGF-A expression and angiogenesis involved the FAK, c-Src and PKC delta signaling pathways, while miR-206 expression was negatively mediated by AR via the FAK, c-Src and PKC delta pathways. Our results illustrate the clinical significance between AR, VEGF-A and miR-206, as well as tumor stage, in human chondrosarcoma. AR may represent a novel therapeutic target in the metastasis and angiogenesis of chondrosarcoma. (C) 2016 Elsevier Ireland Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据