Mboge Mam Y, Mahon Brian P, McKenna Robert, Frost Susan C
University of Florida, College of Medicine, Department of Biochemistry and Molecular Biology, P.O. Box 100245, Gainesville, FL 32610, USA.
Metabolites. 2018 Feb 28;8(1):19. doi: 10.3390/metabo8010019.
The pH of the tumor microenvironment drives the metastatic phenotype and chemotherapeutic resistance of tumors. Understanding the mechanisms underlying this pH-dependent phenomenon will lead to improved drug delivery and allow the identification of new therapeutic targets. This includes an understanding of the role pH plays in primary tumor cells, and the regulatory factors that permit cancer cells to thrive. Over the last decade, carbonic anhydrases (CAs) have been shown to be important mediators of tumor cell pH by modulating the bicarbonate and proton concentrations for cell survival and proliferation. This has prompted an effort to inhibit specific CA isoforms, as an anti-cancer therapeutic strategy. Of the 12 active CA isoforms, two, CA IX and XII, have been considered anti-cancer targets. However, other CA isoforms also show similar activity and tissue distribution in cancers and have not been considered as therapeutic targets for cancer treatment. In this review, we consider all the CA isoforms and their possible role in tumors and their potential as targets for cancer therapy.
肿瘤微环境的pH值驱动肿瘤的转移表型和化疗耐药性。了解这种pH依赖性现象背后的机制将改善药物递送,并有助于确定新的治疗靶点。这包括了解pH值在原发性肿瘤细胞中所起的作用,以及使癌细胞得以生长的调节因子。在过去十年中,碳酸酐酶(CAs)已被证明是肿瘤细胞pH值的重要调节因子,通过调节碳酸氢盐和质子浓度来维持细胞存活和增殖。这促使人们努力抑制特定的CA同工型,作为一种抗癌治疗策略。在12种活性CA同工型中,CA IX和CA XII这两种同工型被视为抗癌靶点。然而,其他CA同工型在癌症中也表现出类似的活性和组织分布,但尚未被视为癌症治疗的靶点。在这篇综述中,我们考虑了所有的CA同工型及其在肿瘤中的可能作用以及作为癌症治疗靶点的潜力。