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血小板反应蛋白-1对肿瘤血管生成的调节作用

Regulation of tumor angiogenesis by thrombospondin-1.

作者信息

Ren Bin, Yee Karen O, Lawler Jack, Khosravi-Far Roya

机构信息

Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.

出版信息

Biochim Biophys Acta. 2006 Apr;1765(2):178-88. doi: 10.1016/j.bbcan.2005.11.002. Epub 2005 Dec 21.

Abstract

Angiogenesis plays a critical role in the growth and metastasis of tumors. Thrombospondin-1 (TSP-1) is a potent angiogenesis inhibitor, and down-regulation of TSP-1 has been suggested to alter tumor growth by modulating angiogenesis in a variety of tumor types. Expression of TSP-1 is up-regulated by the tumor suppressor gene, p53, and down-regulated by oncogenes such as Myc and Ras. TSP-1 inhibits angiogenesis by inhibiting endothelial cell migration and proliferation and by inducing apoptosis. In addition, activation of transforming growth factor beta (TGF-beta) by TSP-1 plays a crucial role in the regulation of tumor progression. An understanding of the molecular basis of TSP-1-mediated inhibition of angiogenesis and tumor progression will aid in the development of novel therapeutics for the treatment of cancer.

摘要

血管生成在肿瘤的生长和转移中起着关键作用。血小板反应蛋白-1(TSP-1)是一种有效的血管生成抑制剂,有人提出TSP-1的下调可通过调节多种肿瘤类型中的血管生成来改变肿瘤生长。TSP-1的表达受肿瘤抑制基因p53上调,受Myc和Ras等癌基因下调。TSP-1通过抑制内皮细胞迁移和增殖以及诱导凋亡来抑制血管生成。此外,TSP-1激活转化生长因子β(TGF-β)在肿瘤进展的调节中起关键作用。了解TSP-1介导的血管生成抑制和肿瘤进展的分子基础将有助于开发治疗癌症的新型疗法。

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