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微管蛋白结合剂的作用机制及耐药性

Mechanisms of action and resistance to tubulin-binding agents.

作者信息

Dumontet C

机构信息

Service d'Hématologie, Centre Hospitalier Lyon Sud, 69495 Pierre Bénite Cedex, France.

出版信息

Expert Opin Investig Drugs. 2000 Apr;9(4):779-88. doi: 10.1517/13543784.9.4.779.

Abstract

Tubulin binding agents constitute an important class of antimitotics and are widely used for the treatment of solid tumours an haematopoietic malignancies. These compounds, currently represented by the vinca alkaloids and the taxanes, differ from most of the other clinically useful antimitotics in that their target is not nucleic acids, but the mitotic spindle, which is an essential component of the mitotic machinery. Recent data on the mechanisms of action of and mechanisms of resistance to tubulin binding agents are presented. The importance of microtubule dynamics is emphasised, in particular in relationship to the usefulness of drug combinations. Concerning the reported resistance mechanisms, an emerging body of data show that altered microtubule structure may be involved in reduced sensitivity to these compounds. Promising new molecules, including those derived from marine organisms are described.

摘要

微管蛋白结合剂是一类重要的抗有丝分裂药物,广泛用于治疗实体瘤和血液系统恶性肿瘤。目前以长春花生物碱和紫杉烷为代表的这些化合物,与大多数其他临床上有用的抗有丝分裂药物不同,因为它们的靶点不是核酸,而是有丝分裂纺锤体,有丝分裂纺锤体是有丝分裂机制的重要组成部分。本文介绍了微管蛋白结合剂的作用机制和耐药机制的最新数据。强调了微管动力学的重要性,特别是与联合用药的有效性相关。关于已报道的耐药机制,越来越多的数据表明,微管结构改变可能与对这些化合物的敏感性降低有关。本文还描述了有前景的新分子,包括那些源自海洋生物的分子。

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