肿瘤血管生成与血管细胞整合素的作用。

Important advances in oncology Pub Date : 1996-01-01
J A Varner, D A Cheresh
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引用次数: 0

摘要

血管生成是所有实体瘤生长和转移特性的关键过程。最近的生物学和分子研究已经开始阐明体外和体内血管细胞增殖、运动和分化的基本机制。有了这些知识,设计治疗策略来选择性地靶向和干扰血管生成血管细胞的生物过程,从而导致有效的血管生成抑制剂应该是可行的。这一策略导致了整合素v β 3拮抗剂的发展,它促进了新生血管的计划外程序性细胞死亡。这些拮抗剂可使实验室动物体内生长的预先建立的人类肿瘤消退,因此可能为大多数人类实体肿瘤提供一种有效的治疗方法。目前的研究旨在设计高度特异性的有机小整合素抑制剂,以破坏使血管细胞对肿瘤相关的细胞外环境作出反应的信号,并促进肿瘤诱导的血管生成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumor angiogenesis and the role of vascular cell integrin alphavbeta3.

Angiogenesis is a critical process for the growth and metastatic properties of all solid tumors. Recent biological and molecular studies have begun to elucidate the basic mechanisms of vascular cell proliferation, motility, and differentiation in vitro and in vivo. With this knowledge, it should be feasible to devise therapeutic strategies to selectively target and perturb the biological processes of angiogenic vascular cells, thereby leading to effective inhibitors of angiogenesis. This strategy has led to the development of antagonists to integrin alpha v beta 3, which promote the unscheduled programmed cell death of newly sprouting blood vessels. These antagonists cause regression of preestablished human tumors growing in laboratory animals and thus may lead to an effective therapeutic approach for most solid tumors in humans. Studies are currently aimed at designing highly specific small organic integrin inhibitors that will disrupt the signals enabling vascular cells to respond to the tumor-associated extracellular environment and to promote tumor-induced angiogenesis.

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