在人类疾病中发挥多种作用的粘附 GPCR--GPR56,现状与未来展望。

IF 3 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Yan Fan, Xiao-Yan Yan, Wei Guan
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引用次数: 0

摘要

人类 G 蛋白偶联受体 56(GPR56)属于粘附 G 蛋白偶联受体(aGPCR)家族成员,广泛存在于中枢神经系统和各类肿瘤组织中。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,GPR56 在治疗神经精神疾病和癌症的过程中,已被证明能增强某些抗精神病药物和抗癌药物的易感性。虽然已有一些关于 GPR56 功能的报道,但与这些疾病(尤其是抑郁症和癫痫)相关的潜在机制尚未得到彻底阐明。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。我们的综述显示,GPR56 缺乏会导致抑郁样行为,并增加对抗精神病药物治疗的抵抗力。相反,GPR56 的上调则有助于胶质母细胞瘤、结直肠癌和卵巢癌等恶性疾病中肿瘤细胞的增殖和转移。此外,我们还阐明了 GPR56 下游与这些疾病发病机制相关的特定信号通路。总之,我们的综述提供了令人信服的论据,证明 GPR56 是一个有吸引力的治疗靶点,可以提高精神疾病和癌症患者的治疗效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GPR56, an Adhesion GPCR with Multiple Roles in Human Diseases, Current Status and Future Perspective.

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.

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来源期刊
Current drug targets
Current drug targets 医学-药学
CiteScore
6.20
自引率
0.00%
发文量
127
审稿时长
3-8 weeks
期刊介绍: Current Drug Targets aims to cover the latest and most outstanding developments on the medicinal chemistry and pharmacology of molecular drug targets e.g. disease specific proteins, receptors, enzymes, genes. Current Drug Targets publishes guest edited thematic issues written by leaders in the field covering a range of current topics of drug targets. The journal also accepts for publication mini- & full-length review articles and drug clinical trial studies. As the discovery, identification, characterization and validation of novel human drug targets for drug discovery continues to grow; this journal is essential reading for all pharmaceutical scientists involved in drug discovery and development.
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