Cervantes-Madrid Diana, Romero Yair, Dueñas-González Alfonso
Instituto Nacional de Cancerología, 14080 Mexico City, DF, Mexico.
Facultad de Ciencias, Universidad Nacional Autónoma de México, 04510 Mexico City, DF, Mexico.
Biomed Res Int. 2015;2015:690492. doi: 10.1155/2015/690492. Epub 2015 Sep 6.
Abnormal metabolism is another cancer hallmark. The two most characterized altered metabolic pathways are high rates of glycolysis and glutaminolysis, which are natural targets for cancer therapy. Currently, a number of newer compounds to block glycolysis and glutaminolysis are being developed; nevertheless, lonidamine and 6-diazo-5-oxo-L-norleucine (DON) are two old drugs well characterized as inhibitors of glycolysis and glutaminolysis, respectively, whose clinical development was abandoned years ago when the importance of cancer metabolism was not fully appreciated and clinical trial methodology was less developed. In this review, a PubMed search using the words lonidamine and 6-diazo-5-oxo-L-norleucine (DON) was undertaken to analyse existing information on the preclinical and clinical studies of these drugs for cancer treatment. Data show that they exhibit antitumor effects; besides there is also the suggestion that they are synergistic. We conclude that lonidamine and DON are safe and potentially effective drugs that need to be reevaluated in combination as metabolic therapy of cancer.
代谢异常是癌症的另一个标志。两种最具特征的代谢途径改变是糖酵解和谷氨酰胺分解速率升高,它们是癌症治疗的天然靶点。目前,正在开发许多新型化合物来阻断糖酵解和谷氨酰胺分解;然而,氯尼达明和6-重氮-5-氧代-L-正亮氨酸(DON)是两种老药,分别被明确为糖酵解和谷氨酰胺分解的抑制剂,其临床开发在多年前就被放弃了,当时癌症代谢的重要性尚未得到充分认识,临床试验方法也不够完善。在本综述中,通过在PubMed上搜索氯尼达明和6-重氮-5-氧代-L-正亮氨酸(DON)这两个词,分析了有关这些药物用于癌症治疗的临床前和临床研究的现有信息。数据表明它们具有抗肿瘤作用;此外,也有迹象表明它们具有协同作用。我们得出结论,氯尼达明和DON是安全且可能有效的药物,需要作为癌症代谢疗法联合重新评估。