Borden Katherine L B
Department of Pathology and Cell Biology, Institute for Research in Immunology and Cancer, Université de Montréal, Montréal, Canada.
Cancer Res. 2014 Dec 15;74(24):7175-80. doi: 10.1158/0008-5472.CAN-14-2607. Epub 2014 Dec 4.
Cancer cells rapidly evolve a multitude of defense mechanisms to evade the effects of the oncologist's drug arsenal. Unfortunately, clinical strategies to overcome these lag far behind. This mismatch likely underlies our inability to implement new durable treatment strategies. Here, a new form of multidrug resistance, inducible drug glucuronidation, is discussed. This form was discovered while developing means to target a specific oncogene, the eukaryotic translation initiation factor 4E (eIF4E), with its inhibitor ribavirin. In two clinical studies, ribavirin treatment led to substantial clinical responses, but all responding patients eventually relapsed. In most cases, this was due to the overexpression of the sonic hedgehog transcription factor Gli1, which elevated the UDP glucuronsyltransferase UGT1A enzymes. UGT1As add glucuronic acid to many drugs. Indeed, these cells are resistant to not only ribavirin, but also Ara-C, and likely other drugs. Inhibition of Gli1 reduced UGT1As, eliminated drug glucuronides, and renewed sensitivity to ribavirin and Ara-C. These studies highlight that cancer cells and their resistant counterparts metabolize drugs differently from each other as well as from normal cells. Likely, these inducible modifications go beyond glucuronidation. Understanding the extent of inducible drug modifications and the pathways that drive expression of the corresponding enzymatic machinery will better position us to finally make resistance futile.
癌细胞会迅速进化出多种防御机制,以逃避肿瘤学家药物库的作用。不幸的是,克服这些问题的临床策略远远落后。这种不匹配可能是我们无法实施新的持久治疗策略的根本原因。在此,将讨论一种新形式的多药耐药性,即诱导性药物葡糖醛酸化。这种形式是在开发用利巴韦林抑制特定致癌基因——真核翻译起始因子4E(eIF4E)的方法时发现的。在两项临床研究中,利巴韦林治疗带来了显著的临床反应,但所有有反应的患者最终都复发了。在大多数情况下,这是由于音猬因子转录因子Gli1的过度表达,它会使尿苷二磷酸葡糖醛酸基转移酶UGT1A酶升高。UGT1A会将葡糖醛酸添加到许多药物上。实际上,这些细胞不仅对利巴韦林耐药,对阿糖胞苷也耐药,可能对其他药物也耐药。抑制Gli1可降低UGT1A,消除药物葡糖醛酸化物,并恢复对利巴韦林和阿糖胞苷的敏感性。这些研究突出表明,癌细胞及其耐药对应物对药物的代谢方式与正常细胞不同,也彼此不同。很可能,这些诱导性修饰不仅仅局限于葡糖醛酸化。了解诱导性药物修饰的程度以及驱动相应酶机制表达的途径,将使我们更好地最终使耐药性变得无效。