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前列腺素 EP2 受体:人类癌症的新治疗靶点(综述)。

Prostaglandin EP2 receptor: Novel therapeutic target for human cancers (Review).

机构信息

Department of Medical Oncology and Cancer Institute of Integrative Medicine, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, P.R. China.

出版信息

Int J Mol Med. 2018 Sep;42(3):1203-1214. doi: 10.3892/ijmm.2018.3744. Epub 2018 Jun 26.

Abstract

Prostaglandin E2 (PGE2) receptor 2 subtype (EP2), which is a metabolite of arachidonic acid that binds with and regulates cellular responses to PGE2, is associated with numerous physiological and pathological events in a wide range of tissues. As a stimulatory G protein‑coupled receptor, PGE2‑induced EP2 activation can activate adenylate cyclase, leading to increased cytoplasmic cAMP levels and activation of protein kinase A. The EP2 receptor can also activate the glycogen synthase kinase 3β and β‑catenin pathways. The present study aimed to review the roles of the EP2 receptor in tumor development, including immunity, chronic inflammation, angiogenesis, metastasis and multidrug resistance. Furthermore, the involvement of the EP2 receptor signaling pathway in cancer was discussed. Understanding the role and mechanisms of action of the EP2 receptor, and its importance in targeted therapy, may help identify novel methods to improve management of numerous types of cancer.

摘要

前列腺素 E2(PGE2)受体 2 亚型(EP2)是花生四烯酸的代谢产物,与 PGE2 结合并调节细胞对其的反应,与广泛组织中的许多生理和病理事件有关。作为一种刺激 G 蛋白偶联受体,PGE2 诱导的 EP2 激活可激活腺苷酸环化酶,导致细胞浆 cAMP 水平升高和蛋白激酶 A 的激活。EP2 受体还可以激活糖原合酶激酶 3β和β-连环蛋白途径。本研究旨在综述 EP2 受体在肿瘤发展中的作用,包括免疫、慢性炎症、血管生成、转移和多药耐药性。此外,还讨论了 EP2 受体信号通路在癌症中的作用。了解 EP2 受体的作用和作用机制及其在靶向治疗中的重要性,可能有助于确定改善多种类型癌症治疗的新方法。

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