Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, MD 20892, USA.
Curr Pharm Biotechnol. 2011 Apr;12(4):609-20. doi: 10.2174/138920111795163887.
Multidrug resistance caused by the overexpression of ABC drug transporters is a major obstacle in clinical cancer chemotherapy. For several years, it appeared that direct inhibition of ABC transporters would be the cheapest and most efficient way to combat this problem. Unfortunately, progress in finding a potent, selective inhibitor to modulate ABC transporters and restore drug sensitivity in multidrug-resistant cancer cells has been slow and challenging. Candidate drugs should ideally be selective, potent and relatively non-toxic. Many researchers in recent years have turned their attention to utilizing natural products as the building blocks for the development of the next generation of inhibitors, especially after the disappointing results obtained from inhibitors of the first three generations at the clinical trial stage. The first step is to discover natural substances (distinct from the first three generation inhibitors) that are potent, selective and relatively non-toxic in order to be used clinically. Here, we present a brief overview of the prospect of using natural products to modulate the function of ABC drug transporters clinically and their impact on human physiology and pharmacology.
多药耐药性是由 ABC 药物转运蛋白的过度表达引起的,是临床癌症化疗的主要障碍。多年来,直接抑制 ABC 转运蛋白似乎是解决这一问题的最便宜、最有效的方法。不幸的是,寻找一种有效的、选择性的抑制剂来调节 ABC 转运蛋白并恢复多药耐药癌细胞的药物敏感性的进展缓慢且具有挑战性。候选药物在理想情况下应该是选择性的、有效的且相对无毒的。近年来,许多研究人员将注意力转向利用天然产物作为开发下一代抑制剂的基础,尤其是在第一代至第三代抑制剂在临床试验阶段获得令人失望的结果之后。第一步是发现具有强大、选择性和相对无毒的天然物质(与前三代抑制剂不同),以便在临床上使用。在这里,我们简要概述了使用天然产物调节 ABC 药物转运蛋白的功能的临床前景,以及它们对人体生理学和药理学的影响。