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GPR56,一种黏附 GPCR,在人类疾病中具有多种作用,现状和未来展望。

GPR56, an Adhesion GPCR with Multiple Roles in Human Diseases, Current Status and Future Perspective.

机构信息

Department of Pharmacy, Zhangjiagang Second People's Hospital, Zhangjiagang 215600, Jiangsu, China.

Department of Pharmacology, Pharmacy College, Nantong University, Nantong 226001, Jiangsu, China.

出版信息

Curr Drug Targets. 2024;25(8):558-573. doi: 10.2174/0113894501298344240507080149.

Abstract

Human G protein-coupled receptor 56 (GPR56) belongs to a member of the adhesion G-protein coupled receptor (aGPCR) family and widely exists in the central nervous system and various types of tumor tissues. Recent studies have shown that abnormal expression or dysfunction of GPR56 is closely associated with many physiological and pathological processes, including brain development, neuropsychiatric disorders, cardiovascular diseases and cancer progression. In addition, GPR56 has been proven to enhance the susceptibility of some antipsychotics and anticarcinogens in response to the treatment of neuropsychological diseases and cancer. Although there have been some reports about the functions of GPR56, the underlying mechanisms implicated in these diseases have not been clarified thoroughly, especially in depression and epilepsy. Therefore, in this review, we described the molecular structure and signal transduction pathway of GPR56 and carried out a comprehensive summary of GPR56's function in the development of psychiatric disorders and cancer. Our review showed that GPR56 deficiency led to depressive-like behaviors and an increase in resistance to antipsychotic treatment. In contrast, the upregulation of GPR56 contributed to tumor cell proliferation and metastasis in malignant diseases such as glioblastoma, colorectal cancer, and ovarian cancer. Moreover, we elucidated specific signaling pathways downstream of GPR56 related to the pathogenesis of these diseases. In summary, our review provides compelling arguments for an attractive therapeutic target of GPR56 in improving the therapeutic efficiency for patients suffering from psychiatric disorders and cancer.

摘要

人类 G 蛋白偶联受体 56(GPR56)属于黏附 G 蛋白偶联受体(aGPCR)家族的成员,广泛存在于中枢神经系统和各种类型的肿瘤组织中。最近的研究表明,GPR56 的异常表达或功能障碍与许多生理和病理过程密切相关,包括大脑发育、神经精神疾病、心血管疾病和癌症进展。此外,已经证明 GPR56 增强了一些抗精神病药和抗癌药对神经心理疾病和癌症治疗的敏感性。尽管已经有一些关于 GPR56 功能的报道,但这些疾病中涉及的潜在机制尚未得到充分阐明,特别是在抑郁症和癫痫中。因此,在这篇综述中,我们描述了 GPR56 的分子结构和信号转导途径,并对 GPR56 在精神疾病和癌症发展中的功能进行了全面总结。我们的综述表明,GPR56 缺乏导致抑郁样行为和对抗精神病治疗的耐药性增加。相比之下,GPR56 的上调促进了胶质母细胞瘤、结直肠癌和卵巢癌等恶性疾病中的肿瘤细胞增殖和转移。此外,我们阐明了与这些疾病发病机制相关的 GPR56 下游特定信号通路。总之,我们的综述为 GPR56 作为改善精神疾病和癌症患者治疗效果的有吸引力的治疗靶点提供了有力的证据。

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