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第14章. 测量肿瘤内微血管密度

Chapter 14. Measuring intratumoral microvessel density.

作者信息

Weidner Noel

机构信息

Department of Pathology, University of California, San Diego, San Diego, California, USA.

出版信息

Methods Enzymol. 2008;444:305-23. doi: 10.1016/S0076-6879(08)02814-0.

Abstract

For a tumor to grow beyond a limited volume of 1-2 mm(3), the tumor cells must not only proliferate, but they must be able to induce the growth of new capillary blood vessels from the host. As early as 1971, it was proposed that tumor growth was dependent on angiogenesis; and, that tumor cells and blood vessels composed a highly integrated ecosystem, that endothelial cells could be switched from a resting state to one of rapid growth by a diffusible signal from tumor cells, and that anti-angiogenesis may become an effective anti-cancer therapy. Indeed, now there is considerable indirect and direct evidence to show that tumor growth is angiogenesis dependent, that tumor cells can produce diffusible angiogenic regulatory molecules, and that angiogenesis inhibitors can slow or prevent tumor growth, and that angiogenesis is a relevant target for anti-cancer therapy. Measuring intratumoral microvessel density (iMVD) in vascular "hot spots" has been shown to correlate with aggressive tumor behavior. This chapter reviews the techniques available for measuring iMVD.

摘要

肿瘤要生长超过1 - 2立方毫米的有限体积,肿瘤细胞不仅必须增殖,还必须能够诱导宿主产生新的毛细血管。早在1971年,就有人提出肿瘤生长依赖于血管生成;肿瘤细胞和血管构成了一个高度整合的生态系统,内皮细胞可以通过肿瘤细胞发出的可扩散信号从静止状态转变为快速生长状态,并且抗血管生成可能成为一种有效的抗癌疗法。事实上,现在有大量间接和直接证据表明肿瘤生长依赖于血管生成,肿瘤细胞可以产生可扩散的血管生成调节分子,血管生成抑制剂可以减缓或阻止肿瘤生长,并且血管生成是抗癌治疗的一个相关靶点。测量血管“热点”中的肿瘤内微血管密度(iMVD)已被证明与侵袭性肿瘤行为相关。本章综述了可用于测量iMVD的技术。

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