Department of Clinical Biochemistry and Laboratory Medicine, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Genetics, Faculty of Advanced science and Technology, Tehran Medical science, Islamic Azad University, Tehran, Iran.
Asian Pac J Cancer Prev. 2023 May 1;24(5):1817-1825. doi: 10.31557/APJCP.2023.24.5.1817.
In recent years, molecular targeted therapy has attracted more attention from researchers due to its high efficiency and fewer side effects. Researchers are attempting to find more specific ways to treat diseases. It has been found that there are different targets for the treatment of diseases such as cancer, obesity, and metabolic syndrome. It is important to find a potential target in order to lessen the side effects of current treatments. G Protein-coupled receptors (GPCRs) are a large family of transmembrane proteins that are expressed in many organs, leading to the activation of internal signal transduction cascades through the binding of different ligands, including neurotransmitters, peptides, and lipids. Due to the critical role of GPCRs in cells, it could be a potential target. G protein-coupled receptor 75 (GPR75) is a novel member of the GPCR family that has an important role in many diseases, such as obesity, cancer, and metabolic syndrome. Until now, three ligands have been detected for GPR75, including 20-HETE, CCL5, and RANTES. Recent studies suggest that 20-HETE, through GPR75, triggers signaling pathways including PI3K/Akt and RAS/MAPK, leading to a more aggressive phenotype in prostate cancer cells. Additionally, the PI3K/Akt and RAS/MAPK signaling pathways activate NF-κB, which is significant in various pathways of cancer development such as proliferation, migration, and apoptosis. The findings indicate that inhibiting GPR75 in humans leads to an increase in insulin sensitivity and glucose tolerance, as well as a reduction in body fat storage. According to these discoveries, GPR75 could be a potential target for drug treatment of diseases such as obesity, metabolic syndrome, and cancer. In this review, we aimed to discuss the therapeutic impact of GPR75 in cancer, metabolic syndrome, and obesity and underscore the possible pathways.
近年来,由于分子靶向治疗具有高效、低副作用的特点,引起了研究人员的广泛关注。研究人员试图寻找更特异的方法来治疗疾病。已经发现,癌症、肥胖症和代谢综合征等疾病的治疗有不同的靶点。找到一个潜在的靶点对于减轻当前治疗的副作用非常重要。G 蛋白偶联受体(GPCR)是一大类跨膜蛋白,在许多器官中表达,通过与不同配体(包括神经递质、肽和脂质)结合,激活内部信号转导级联反应。由于 GPCR 在细胞中的关键作用,它可能是一个潜在的靶点。G 蛋白偶联受体 75(GPR75)是 GPCR 家族的一个新成员,在肥胖症、癌症和代谢综合征等许多疾病中发挥着重要作用。到目前为止,已经检测到三种配体与 GPR75 结合,包括 20-HETE、CCL5 和 RANTES。最近的研究表明,20-HETE 通过 GPR75 触发包括 PI3K/Akt 和 RAS/MAPK 在内的信号通路,导致前列腺癌细胞更具侵袭性表型。此外,PI3K/Akt 和 RAS/MAPK 信号通路激活 NF-κB,这在癌症发展的各种途径中都很重要,如增殖、迁移和凋亡。这些发现表明,在人类中抑制 GPR75 会导致胰岛素敏感性和葡萄糖耐量增加,同时减少体脂肪储存。根据这些发现,GPR75 可能成为肥胖症、代谢综合征和癌症等疾病药物治疗的潜在靶点。在这篇综述中,我们旨在讨论 GPR75 在癌症、代谢综合征和肥胖症中的治疗作用,并强调可能的途径。