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糖尿病和癌症条件下比较 G 蛋白偶联雌激素受体(GPER)系统:综述。

Comparative G-Protein-Coupled Estrogen Receptor (GPER) Systems in Diabetic and Cancer Conditions: A Review.

机构信息

Center for Cancer Research, Department of Biology, Tuskegee University, Tuskegee, AL 36088, USA.

Department of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria P.M.B. 1044, Nigeria.

出版信息

Molecules. 2022 Dec 15;27(24):8943. doi: 10.3390/molecules27248943.

DOI:10.3390/molecules27248943
PMID:36558071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9786783/
Abstract

For many patients, diabetes Mellitus and Malignancy are frequently encountered comorbidities. Diabetes affects approximately 10.5% of the global population, while malignancy accounts for 29.4 million cases each year. These troubling statistics indicate that current treatment approaches for these diseases are insufficient. Alternative therapeutic strategies that consider unique signaling pathways in diabetic and malignancy patients could provide improved therapeutic outcomes. The G-protein-coupled estrogen receptor (GPER) is receiving attention for its role in disease pathogenesis and treatment outcomes. This review aims to critically examine GPER' s comparative role in diabetes mellitus and malignancy, identify research gaps that need to be filled, and highlight GPER's potential as a therapeutic target for diabetes and malignancy management. There is a scarcity of data on GPER expression patterns in diabetic models; however, for diabetes mellitus, altered expression of transport and signaling proteins has been linked to GPER signaling. In contrast, GPER expression in various malignancy types appears to be complex and debatable at the moment. Current data show inconclusive patterns of GPER expression in various malignancies, with some indicating upregulation and others demonstrating downregulation. Further research should be conducted to investigate GPER expression patterns and their relationship with signaling pathways in diabetes mellitus and various malignancies. We conclude that GPER has therapeutic potential for chronic diseases such as diabetes mellitus and malignancy.

摘要

对于许多患者来说,糖尿病和恶性肿瘤是经常同时出现的并发症。糖尿病影响了全球约 10.5%的人口,而恶性肿瘤每年的病例数则高达 2940 万。这些令人担忧的统计数据表明,目前对这些疾病的治疗方法还不够完善。考虑到糖尿病和恶性肿瘤患者独特信号通路的替代治疗策略可能会提供更好的治疗效果。G 蛋白偶联雌激素受体(GPER)因其在疾病发病机制和治疗结果中的作用而受到关注。本综述旨在批判性地研究 GPER 在糖尿病和恶性肿瘤中的比较作用,确定需要填补的研究空白,并强调 GPER 作为糖尿病和恶性肿瘤管理的治疗靶点的潜力。目前关于糖尿病模型中 GPER 表达模式的数据还很缺乏;然而,对于糖尿病来说,转运和信号蛋白的表达改变与 GPER 信号有关。相比之下,目前 GPER 在各种恶性肿瘤类型中的表达似乎比较复杂,存在争议。目前的数据显示,GPER 在各种恶性肿瘤中的表达模式不一致,有些表明上调,而有些则表明下调。应该进行进一步的研究来调查 GPER 在糖尿病和各种恶性肿瘤中的表达模式及其与信号通路的关系。我们得出结论,GPER 对糖尿病和恶性肿瘤等慢性疾病具有治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f6/9786783/3d4fdfce5825/molecules-27-08943-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f6/9786783/21f9f6244039/molecules-27-08943-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f6/9786783/3d4fdfce5825/molecules-27-08943-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f6/9786783/21f9f6244039/molecules-27-08943-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9f6/9786783/3d4fdfce5825/molecules-27-08943-g002.jpg

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