沙利度胺和类似物:目前提出的机制和治疗用途

W. Nathaniel Brennen , Carlton R. Cooper , Scott Capitosti , Milton L. Brown , Robert A. Sikes
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引用次数: 18

摘要

微血管密度是许多癌症的预后因素,包括前列腺癌。由于这个原因,一些针对肿瘤微血管的研究和治疗方法已经尝试过。沙利度胺一直被认为是一种抗血管生成的分子。最近,这种药物作为抗癌药物重新受到青睐,并在多发性骨髓瘤和前列腺癌等疾病的临床试验中。本文将简要回顾沙利度胺的作用机制,讨论为什么这些作用在目前正在进行临床试验的疾病中具有治疗价值,并总结目前前列腺癌的临床试验现状。重点将主要放在沙利度胺与血管生成的关系上,以及沙利度胺启发的结构衍生物的未来和潜在价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thalidomide and Analogues: Current Proposed Mechanisms and Therapeutic Usage

Microvessel density is a prognostic factor for many cancers, including prostate. For this reason, several studies and therapeutic approaches that target the tumor microvasculature have been attempted. Thalidomide has long been recognized as an antiangiogenic molecule. Recently, this drug has regained favor as an anticancer agent and is in clinical trial for multiple myeloma and prostate cancer, among others. This article will briefly review the proposed mechanisms of action for thalidomide, discuss why these activities are of therapeutic value in diseases currently undergoing clinical trials, and summarize the current status of clinical trials for prostate cancer. The focus will be predominantly on the relationship of thalidomide to angiogenesis, as well as on the future and potential value of thalidomide-inspired structural derivatives.

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