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首页> 外文期刊>Cell death & disease. >Resistin facilitates VEGF-A-dependent angiogenesis by inhibiting miR-16-5p in human chondrosarcoma cells
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Resistin facilitates VEGF-A-dependent angiogenesis by inhibiting miR-16-5p in human chondrosarcoma cells

机译:抵抗素通过抑制人软骨肉瘤细胞中的miR-16-5p促进VEGF-A依赖性血管生成

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摘要

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.
机译:抵抗素是一种与肥胖,炎症和各种癌症有关的脂肪因子。软骨肉瘤是原发性恶性骨肿瘤,预后较差。 VEGF-A是关键的血管生成因子,已知可促进软骨肉瘤中的血管生成和转移。抵抗素是否影响人软骨肉瘤血管生成尚不清楚。在这项研究中,我们显示了抵抗素如何促进VEGF-A的表达并随后诱导内皮祖细胞(EPC)的血管生成。抵抗素治疗激活了磷脂酰肌醇3-激酶(PI3K)和Akt信号通路,而PI3K和Akt抑制剂或siRNA减少了抵抗素诱导的VEGF-A表达。体外和体内研究表明,在抵抗素诱导的VEGF-A表达和EPC血管生成中微RNA(miR)-16-5p的下调。我们还发现软骨肉瘤患者抵抗素与VEGF-A表达之间呈正相关,而抵抗素与VEGF-A与miR-16-5p之间呈负相关。这些发现表明,抵抗素通过经由PI3K / Akt信号传导级联的miR-16-5p表达的抑制来促进VEGF-A表达和血管生成。抵抗素可能是软骨肉瘤血管生成中有希望的靶标。

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