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大麻素受体系统:肿瘤干预的治疗靶点。

Cannabinoid receptor systems: therapeutic targets for tumour intervention.

作者信息

Jones Sarah, Howl John

机构信息

Molecular Pharmacology Group, Biomedical Sciences Division, School of Applied Sciences, University of Wolverhampton, Wulfruna Street, WV1 1SB, UK.

出版信息

Expert Opin Ther Targets. 2003 Dec;7(6):749-58. doi: 10.1517/14728222.7.6.749.

DOI:10.1517/14728222.7.6.749
PMID:14640910
Abstract

The past decade has witnessed a rapid expansion of our understanding of the biological roles of cannabinoids and their cognate receptors. It is now certain that Delta9-tetrahydrocannabinol, the principle psychoactive component of the Cannabis sativa plant, binds and activates membrane receptors of the 7-transmembrane domain, G-protein-coupled superfamily. Several putative endocannabinoids have since been identified, including anandamide, 2-arachidonyl glycerol and noladin ether. Synthesis of numerous cannabinomimetics has also greatly expanded the repertoire of cannabinoid receptor ligands with the pharmacodynamic properties of agonists, antagonists and inverse agonists. Collectively, these ligands have proven to be powerful tools both for the molecular characterisation of cannabinoid receptors and the delineation of their intrinsic signalling pathways. Much of our understanding of the signalling mechanisms activated by cannabinoids is derived from studies of receptors expressed by tumour cells; hence, this review provides a succinct summary of the molecular pharmacology of cannabinoid receptors and their roles in tumour cell biology. Moreover, there is now a genuine expectation that the manipulation of cannabinoid receptor systems may have therapeutic potential for a diverse range of human diseases. Thus, this review also summarises the demonstrated antitumour actions of cannabinoids and indicates possible avenues for the future development of cannabinoids as antitumour agents.

摘要

在过去十年中,我们对大麻素及其同源受体的生物学作用的理解迅速扩展。现在已经确定,大麻植物的主要精神活性成分Δ9-四氢大麻酚能结合并激活7跨膜结构域、G蛋白偶联超家族的膜受体。此后,已鉴定出几种假定的内源性大麻素,包括花生四烯乙醇胺、2-花生四烯酸甘油和诺拉汀醚。大量大麻模拟物的合成也极大地扩展了具有激动剂、拮抗剂和反向激动剂药效学特性的大麻素受体配体库。总的来说,这些配体已被证明是用于大麻素受体分子表征及其内在信号通路描绘的有力工具。我们对大麻素激活的信号机制的许多理解都来自对肿瘤细胞表达的受体的研究;因此,本综述简要总结了大麻素受体的分子药理学及其在肿瘤细胞生物学中的作用。此外,现在人们真正期望对大麻素受体系统的操纵可能对多种人类疾病具有治疗潜力。因此,本综述还总结了已证实的大麻素的抗肿瘤作用,并指出了大麻素作为抗肿瘤药物未来发展的可能途径。

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Cannabinoid receptor systems: therapeutic targets for tumour intervention.大麻素受体系统:肿瘤干预的治疗靶点。
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