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整合素抑制剂

Inhibitors of integrins.

作者信息

Tucker Gordon C

机构信息

Institut de Recherches Servier, 11 rue des Moulineaux, 92150, Suresnes, France.

出版信息

Curr Opin Pharmacol. 2002 Aug;2(4):394-402. doi: 10.1016/s1471-4892(02)00175-3.

Abstract

The inhibition of integrins--cell surface receptors with a crucial role in angiogenesis, tumour cell survival, invasion and metastases--has centred on the alpha(v)beta3 integrin. Work has culminated in two antagonists that are in clinical trials as cancer therapeutics. Other integrins appear to be candidate targets in the light of gene knockout studies. Surprisingly, genetic alpha(v)beta3 ablation did not confirm the pertinence of the use of alpha(v)beta3 antagonists. However, these apparent discrepancies could be explained by the new finding that this integrin has a role as a cell survival sensor, limiting rather than promoting angiogenesis. Accumulating data on the role of integrins and the mechanism of action of pharmacological antagonists will help to develop and apply an efficient anti-integrin therapy in cancer.

摘要

整联蛋白是在血管生成、肿瘤细胞存活、侵袭和转移中起关键作用的细胞表面受体,对整联蛋白的抑制主要集中在α(v)β3整联蛋白上。研究工作最终产生了两种作为癌症治疗药物正在进行临床试验的拮抗剂。根据基因敲除研究,其他整联蛋白似乎也是候选靶点。令人惊讶的是,基因敲除α(v)β3并未证实使用α(v)β3拮抗剂的相关性。然而,这些明显的差异可以通过这一整联蛋白作为细胞存活传感器发挥作用、限制而非促进血管生成这一新发现来解释。关于整联蛋白作用和药理拮抗剂作用机制的累积数据将有助于开发和应用有效的癌症抗整联蛋白疗法。

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