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利用基因组阐明癌症发病机制中的 G 蛋白偶联受体。

Harnessing the genome for characterization of G-protein coupled receptors in cancer pathogenesis.

机构信息

Cold Spring Harbor Laboratory, NY, USA.

出版信息

FEBS J. 2013 Oct;280(19):4729-38. doi: 10.1111/febs.12473. Epub 2013 Sep 2.

Abstract

G-protein coupled receptors (GPCRs) mediate numerous physiological processes and represent the targets for a vast array of therapeutics for diseases ranging from depression to hypertension to reflux. Despite the recognition that GPCRs can act as oncogenes and tumour suppressors by regulating oncogenic signalling networks, few drugs targeting GPCRs are utilized in cancer therapy. Recent large-scale genome-wide analyses of multiple human tumours have uncovered novel GPCRs altered in cancer. However, work aiming to determine which GPCRs from these lists are the drivers of tumourigenesis, and hence valid therapeutic targets, comprises a formidable challenge. The present review highlights recent studies providing evidence that GPCRs are relevant targets for cancer therapy through their effects on known cancer signalling pathways, tumour progression, invasion and metastasis, and the microenvironment. Furthermore, the review also explores how genomic analysis is beginning to highlight GPCRs as therapeutic targets in the age of personalized medicine.

摘要

G 蛋白偶联受体(GPCRs)介导多种生理过程,是治疗从抑郁症到高血压到反流等各种疾病的广泛治疗靶点。尽管人们已经认识到 GPCRs 可以通过调节致癌信号网络作为癌基因和肿瘤抑制基因发挥作用,但很少有针对 GPCRs 的药物用于癌症治疗。最近对多种人类肿瘤的大规模全基因组分析揭示了在癌症中改变的新型 GPCR。然而,旨在确定这些列表中的哪些 GPCR 是致癌的驱动因素,因此是有效的治疗靶点的工作,构成了一个艰巨的挑战。本综述强调了最近的研究证据,表明 GPCR 通过其对已知癌症信号通路、肿瘤进展、侵袭和转移以及微环境的影响,成为癌症治疗的相关靶点。此外,该综述还探讨了基因组分析如何开始将 GPCR 作为个性化医学时代的治疗靶点。

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