Fiume Luigi, Manerba Marcella, Vettraino Marina, Di Stefano Giuseppina
Department of Experimental, Diagnostic & Specialty Medicine, University of Bologna, via San Giacomo, 14-40126 Bologna, Italy.
Future Med Chem. 2014 Mar;6(4):429-45. doi: 10.4155/fmc.13.206.
In the attempt of developing innovative anticancer treatments, growing interest has recently focused on the peculiar metabolic properties of cancer cells. In this context, LDH, which converts pyruvate to lactate at the end of glycolysis, is emerging as one of the most interesting molecular targets for the development of new inhibitors. In fact, because LDH activity is not needed for pyruvate metabolism through the TCA cycle, inhibitors of this enzyme should spare glucose metabolism of normal non-proliferating cells, which usually completely degrade the glucose molecule to CO2. This review is aimed at summarizing the available data on LDH biology in normal and neoplastic cells, which support the anticancer therapeutic approach based on LDH inhibition. These data encouraged pharmaceutical industries and academic institutions in the search of small-molecule inhibitors and promising candidates have recently been identified. The availability of inhibitors with drug-like properties will allow the evaluation in the near future of the real potential of LDH inhibition in anticancer treatment, also making the identification of the most responsive neoplastic conditions possible.
在开发创新型抗癌治疗方法的尝试中,近来人们越来越关注癌细胞独特的代谢特性。在此背景下,在糖酵解末端将丙酮酸转化为乳酸的乳酸脱氢酶(LDH),正成为开发新型抑制剂最受关注的分子靶点之一。事实上,由于通过三羧酸循环进行丙酮酸代谢并不需要LDH活性,这种酶的抑制剂应不会影响正常非增殖细胞的葡萄糖代谢,正常非增殖细胞通常会将葡萄糖分子完全降解为二氧化碳。这篇综述旨在总结关于正常细胞和肿瘤细胞中LDH生物学的现有数据,这些数据支持基于LDH抑制的抗癌治疗方法。这些数据促使制药行业和学术机构寻找小分子抑制剂,最近已确定了有前景的候选物。具有类药物性质的抑制剂的出现,将使在不久的将来评估LDH抑制在抗癌治疗中的实际潜力成为可能,也使识别最敏感的肿瘤情况成为可能。