MolecularModelling Lab (MML), Department of Pharmaceutical Sciences and Drug Research, Punjabi University , Patiala , India.
Department of Chemistry, Bar-IIan University , Ramat Gan , Israel.
Drug Metab Rev. 2019 May;51(2):196-223. doi: 10.1080/03602532.2019.1632886. Epub 2019 Jul 1.
Regardless of continuous research to develop effective chemotherapies and improve patient's prognosis, cancer still remains one of the most deadly diseases worldwide. The reduction in the pace of successfully developing an effective anti-cancer drug is due to the rapid emergence of drug resistance exhibited by tumor cells. One of the resistance mechanisms which is least considered and somewhat overlooked is chemoresistance via drug metabolizing enzymes (DMEs). Therefore, this review emphasizes on pharmacokinetic resistance specifically the DMEs associated chemoresistance, in which drug molecule is rapidly metabolized by DMEs resulting in diminished potential of anti-cancer drugs. The current review will be covering DMEs that are associated with chemoresistance such as ALDH1A1, GST-π, DPD, CYP1B1 and so forth. Although several strategies have been developed to solve this problem such as prodrug designing, analog designing, DMEs inhibitors designing and development of specific pharmaceutical formulations but the inhibition of DMEs is still not considered significantly. Considering the significance of DMEs in chemoresistance, this review shed light on the mechanism of DMEs associated resistance at molecular level, their reported inhibitors that can be used as an adjuvant therapy and strategies (like prodrug designing, analog designing etc.) used so far to combat this problem.
尽管不断进行研究以开发有效的化疗药物并改善患者的预后,但癌症仍然是全球最致命的疾病之一。成功开发有效抗癌药物的步伐放缓,是由于肿瘤细胞迅速表现出耐药性。耐药机制之一是药物代谢酶(DMEs)介导的化疗耐药性,这一机制尚未得到充分考虑,也有些被忽视。因此,本篇综述重点介绍了药代动力学耐药性,特别是与 DMEs 相关的化疗耐药性,即药物分子被 DMEs 迅速代谢,从而降低了抗癌药物的潜在效果。本篇综述将涵盖与化疗耐药性相关的 DMEs,如 ALDH1A1、GST-π、DPD、CYP1B1 等。尽管已经开发了几种策略来解决这个问题,如前药设计、类似物设计、DMEs 抑制剂设计和特定药物制剂的开发,但 DMEs 的抑制作用仍未得到充分考虑。鉴于 DMEs 在化疗耐药性中的重要性,本篇综述从分子水平上阐明了 DMEs 相关耐药性的机制、已报道的可用作辅助治疗的抑制剂,以及迄今为止用于解决该问题的策略(如前药设计、类似物设计等)。