Institute of Pharmaceutical Sciences, Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology Zürich, Wolfgang Pauli Strasse 10, CH-8093, Zürich, Switzerland.
Nat Rev Drug Discov. 2011 Sep 16;10(10):767-77. doi: 10.1038/nrd3554.
The high metabolic rate of tumours often leads to acidosis and hypoxia in poorly perfused regions. Tumour cells have thus evolved the ability to function in a more acidic environment than normal cells. Key pH regulators in tumour cells include: isoforms 2, 9 and 12 of carbonic anhydrase, isoforms of anion exchangers, Na+/HCO3- co-transporters, Na+/H+ exchangers, monocarboxylate transporters and the vacuolar ATPase. Both small molecules and antibodies targeting these pH regulators are currently at various stages of clinical development. These antitumour mechanisms are not exploited by the classical cancer drugs and therefore represent a new anticancer drug discovery strategy.
肿瘤的高代谢率常常导致血流灌注不良区域的酸中毒和缺氧。肿瘤细胞因此进化出了在比正常细胞更酸性的环境中发挥功能的能力。肿瘤细胞中的关键 pH 调节剂包括:碳酸酐酶同工型 2、9 和 12、阴离子交换体同工型、Na+/HCO3-共转运体、Na+/H+交换体、单羧酸转运体和液泡型 ATP 酶。针对这些 pH 调节剂的小分子和抗体目前处于临床开发的不同阶段。这些抗肿瘤机制未被经典的癌症药物所利用,因此代表了一种新的抗癌药物发现策略。
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