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癌症、化学与细胞:与神经降压素受体相互作用的分子。

Cancer, chemistry, and the cell: molecules that interact with the neurotensin receptors.

作者信息

Myers Rebecca M, Shearman James W, Kitching Matthew O, Ramos-Montoya Antonio, Neal David E, Ley Steven V

机构信息

Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, United Kingdom.

出版信息

ACS Chem Biol. 2009 Jul 17;4(7):503-25. doi: 10.1021/cb900038e.

Abstract

The literature covering neurotensin (NT) and its signalling pathways, receptors, and biological profile is complicated by the fact that the discovery of three NT receptor subtypes has come to light only in recent years. Moreover, a lot of this literature explores NT in the context of the central nervous system and behavioral studies. However, there is now good evidence that the up-regulation of NT is intimately involved in cancer development and progression. This Review aims to summarize the isolation, cloning, localization, and binding properties of the accepted receptor subtypes (NTR1, NTR2, and NTR3) and the molecules known to bind at these receptors. The growing role these targets are playing in cancer research is also discussed. We hope this Review will provide a useful overview and a one-stop resource for new researchers engaged in this field at the chemistry-biology interface.

摘要

由于近年来才发现三种神经降压素(NT)受体亚型,有关NT及其信号通路、受体和生物学特性的文献变得复杂起来。此外,许多此类文献是在中枢神经系统和行为研究的背景下探讨NT的。然而,现在有充分的证据表明,NT的上调与癌症的发生和发展密切相关。本综述旨在总结公认的受体亚型(NTR1、NTR2和NTR3)的分离、克隆、定位和结合特性,以及已知与这些受体结合的分子。还讨论了这些靶点在癌症研究中日益重要的作用。我们希望本综述能为在化学生物学交叉领域从事该研究的新研究人员提供有用的概述和一站式资源。

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