Justus Calvin R, Dong Lixue, Yang Li V
Department of Oncology, Brody School of Medicine, East Carolina University Greenville, NC, USA.
Department of Oncology, Brody School of Medicine, East Carolina University Greenville, NC, USA ; Department of Internal Medicine, Brody School of Medicine, East Carolina University Greenville, NC, USA ; Department of Anatomy and Cell Biology, Brody School of Medicine, East Carolina University Greenville, NC, USA.
Front Physiol. 2013 Dec 5;4:354. doi: 10.3389/fphys.2013.00354.
The tumor microenvironment is acidic due to glycolytic cancer cell metabolism, hypoxia, and deficient blood perfusion. It is proposed that acidosis in the tumor microenvironment is an important stress factor and selection force for cancer cell somatic evolution. Acidic pH has pleiotropic effects on the proliferation, migration, invasion, metastasis, and therapeutic response of cancer cells and the function of immune cells, vascular cells, and other stromal cells. However, the molecular mechanisms by which cancer cells and stromal cells sense and respond to acidic pH in the tumor microenvironment are poorly understood. In this article the role of a family of pH-sensing G protein-coupled receptors (GPCRs) in tumor biology is reviewed. Recent studies show that the pH-sensing GPCRs, including GPR4, GPR65 (TDAG8), GPR68 (OGR1), and GPR132 (G2A), regulate cancer cell metastasis and proliferation, immune cell function, inflammation, and blood vessel formation. Activation of the proton-sensing GPCRs by acidosis transduces multiple downstream G protein signaling pathways. Since GPCRs are major drug targets, small molecule modulators of the pH-sensing GPCRs are being actively developed and evaluated. Research on the pH-sensing GPCRs will continue to provide important insights into the molecular interaction between tumor and its acidic microenvironment and may identify new targets for cancer therapy and chemoprevention.
由于癌细胞的糖酵解代谢、缺氧和血液灌注不足,肿瘤微环境呈酸性。有人提出,肿瘤微环境中的酸中毒是癌细胞体细胞进化的重要应激因素和选择力量。酸性pH值对癌细胞的增殖、迁移、侵袭、转移和治疗反应以及免疫细胞、血管细胞和其他基质细胞的功能具有多效性作用。然而,癌细胞和基质细胞感知并响应肿瘤微环境中酸性pH值的分子机制仍知之甚少。本文综述了一类pH敏感的G蛋白偶联受体(GPCRs)在肿瘤生物学中的作用。最近的研究表明,pH敏感的GPCRs,包括GPR4、GPR65(TDAG8)、GPR68(OGR1)和GPR132(G2A),调节癌细胞的转移和增殖、免疫细胞功能、炎症和血管形成。酸中毒激活质子敏感的GPCRs可转导多个下游G蛋白信号通路。由于GPCRs是主要的药物靶点,目前正在积极开发和评估pH敏感GPCRs的小分子调节剂。对pH敏感GPCRs的研究将继续为肿瘤与其酸性微环境之间的分子相互作用提供重要见解,并可能为癌症治疗和化学预防确定新的靶点。