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GPR68: An Emerging Drug Target in Cancer.
Wiley, Shu Z; Sriram, Krishna; Salmerón, Cristina; Insel, Paul A.
Afiliação
  • Wiley SZ; Department of Pharmacology, University of California, San Diego, La Jolla, CA 92093, USA. szwiley@ucsd.edu.
  • Sriram K; Department of Pharmacology, University of California, San Diego, La Jolla, CA 92093, USA. ksriram@ucsd.edu.
  • Salmerón C; Department of Pharmacology, University of California, San Diego, La Jolla, CA 92093, USA. crsalmeronsalvador@ucsd.edu.
  • Insel PA; Department of Pharmacology, University of California, San Diego, La Jolla, CA 92093, USA. pinsel@ucsd.edu.
Int J Mol Sci ; 20(3)2019 Jan 28.
Article em En | MEDLINE | ID: mdl-30696114
ABSTRACT
GPR68 (or ovarian cancer G protein-coupled receptor 1, OGR1) is a proton-sensing G-protein-coupled receptor (GPCR) that responds to extracellular acidity and regulates a variety of cellular functions. Acidosis is considered a defining hallmark of the tumor microenvironment (TME). GPR68 expression is highly upregulated in numerous types of cancer. Emerging evidence has revealed that GPR68 may play crucial roles in tumor biology, including tumorigenesis, tumor growth, and metastasis. This review summarizes current knowledge regarding GPR68-its expression, regulation, signaling pathways, physiological roles, and functions it regulates in human cancers (including prostate, colon and pancreatic cancer, melanoma, medulloblastoma, and myelodysplastic syndrome). The findings provide evidence for GPR68 as a potentially novel therapeutic target but in addition, we note challenges in developing drugs that target GPR68.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Acoplados a Proteínas G / Terapia de Alvo Molecular / Neoplasias Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Acoplados a Proteínas G / Terapia de Alvo Molecular / Neoplasias Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article