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Pathological significance of vascular endothelial growth factor A isoform expression in human cancer.

机译:人体血管内皮生长因子A同工型表达的病理意义。

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摘要

Vascular endothelial growth factor (VEGF) is a highly specific factor for vascular endothelial cells. Five VEGF-A isoforms (splice variants 121, 145, 165, 189 and 206) are generated as a result of alternative splicing from a single VEGF-A gene. These differ in their molecular weights and in biological properties such as their ability to bind to cell-surface heparan sulfate proteoglycans. Deregulated VEGF-A expression contributes to the development of solid tumors by promoting tumor angiogenesis. More specifically, VEGF-A189 expression is related to angiogenesis and prognosis in certain human solid tumors. VEGF-A189 expression is also related to the xenotransplantability of human cancers into immunodeficient mice in vivo. Consequently, inhibition of VEGF-A or VEGF-A189 signaling regulates the development and metastasis of a variety of tumors. This review focuses on recent studies of the mechanisms by which VEGF-A regulates angiogenesis in the cancer stroma and on our recent findings concerning the potential mechanisms of VEGF-A189 expression on tumor growth and metastasis.
机译:血管内皮生长因子(VEGF)是血管内皮细胞的高度特异性因子。由于从单个VEGF-A基因进行选择性剪接,产生了五种VEGF-A同种型(剪接变体121、145、165、189和206)。它们的分子量和生物学性质不同,例如它们与细胞表面硫酸乙酰肝素蛋白聚糖结合的能力不同。失调的VEGF-A表达通过促进肿瘤血管生成而促进实体瘤的发展。更具体地说,VEGF-A189的表达与某些人实体瘤中的血管生成和预后有关。 VEGF-A189的表达还与人类癌症在体内对免疫缺陷小鼠的异种移植能力有关。因此,抑制VEGF-A或VEGF-A189信号传导调节多种肿瘤的发生和转移。这篇综述着重于VEGF-A调节癌症基质中血管生成的机制的最新研究,以及我们关于VEGF-A189表达对肿瘤生长和转移的潜在机制的最新发现。

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