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Comparative G-Protein-Coupled Estrogen Receptor (GPER) Systems in Diabetic and Cancer Conditions: A Review.
Muhammad, Aliyu; Forcados, Gilead Ebiegberi; Yusuf, Abdurrahman Pharmacy; Abubakar, Murtala Bello; Sadiq, Idris Zubairu; Elhussin, Isra; Siddique, Md Abu Talha; Aminu, Suleiman; Suleiman, Rabiatu Bako; Abubakar, Yakubu Saddeeq; Katsayal, Babangida Sanusi; Yates, Clayton C; Mahavadi, Sunila.
Afiliação
  • Muhammad A; Center for Cancer Research, Department of Biology, Tuskegee University, Tuskegee, AL 36088, USA.
  • Forcados GE; Department of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria P.M.B. 1044, Nigeria.
  • Yusuf AP; Biochemistry Division, National Veterinary Research Institute, Vom P.M.B. 01, Nigeria.
  • Abubakar MB; Department of Biochemistry, School of Life Sciences, Federal University of Technology, Minna P.M.B. 65, Nigeria.
  • Sadiq IZ; Department of Physiology, Faculty of Basic Medical Sciences, College of Health Sciences, Usmanu Danfodiyo University, Sokoto P.M.B. 2254, Nigeria.
  • Elhussin I; Centre for Advanced Medical Research & Training (CAMRET), Usmanu Danfodiyo University, Sokoto P.M.B. 2254, Nigeria.
  • Siddique MAT; Department of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria P.M.B. 1044, Nigeria.
  • Aminu S; Center for Cancer Research, Department of Biology, Tuskegee University, Tuskegee, AL 36088, USA.
  • Suleiman RB; Center for Cancer Research, Department of Biology, Tuskegee University, Tuskegee, AL 36088, USA.
  • Abubakar YS; Department of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria P.M.B. 1044, Nigeria.
  • Katsayal BS; Department of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria P.M.B. 1044, Nigeria.
  • Yates CC; Department of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria P.M.B. 1044, Nigeria.
  • Mahavadi S; Department of Biochemistry, Faculty of Life Sciences, Ahmadu Bello University, Zaria P.M.B. 1044, Nigeria.
Molecules ; 27(24)2022 Dec 15.
Article em En | MEDLINE | ID: mdl-36558071
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diabetes Mellitus / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article