University of Texas M. D. Anderson Cancer Center, Department of Epidemiology, Houston, TX 77030, USA.
Expert Opin Drug Metab Toxicol. 2009 Jul;5(7):745-55. doi: 10.1517/17425250902973711.
NSCLC is the leading cause of cancer-related death in the US. Patients with NSCLC are mostly treated with platinum-based chemotherapy, often in combination with radiation therapy. However, the development of chemo-resistance is a major hurdle limiting treatment success. In this review, we summarize the current understanding of the genetic factors modulating chemoresistance to platinum chemotherapeutics and their association with clinical outcomes for NSCLC patients. We focus on candidate pathways responsible for drug influx and efflux, metabolism and detoxification, DNA damage repair, and other downstream cellular processes that modulate the effect of platinum-based therapy. We also discuss the application of pathway-based polygenic and genome-wide approaches in identifying genetic factors involved in NSCLC clinical outcomes. Overall, current studies have shown that the effects of each individual polymorphism on clinical outcomes are modest suggesting that a more comprehensive approach that incorporates polygenetic, phenotypic, epidemiologic and clinical variables will be necessary to predict prognosis for NSCLC patients receiving platinum-based chemotherapeutics.
非小细胞肺癌是美国癌症相关死亡的主要原因。大多数非小细胞肺癌患者接受铂类化疗,通常与放射治疗联合使用。然而,化疗耐药的发展是限制治疗成功的主要障碍。在这篇综述中,我们总结了目前对调节铂类化疗药物耐药性的遗传因素的理解,以及它们与非小细胞肺癌患者临床结局的关系。我们重点讨论了负责药物内流和外排、代谢和解毒、DNA 损伤修复以及其他调节铂类治疗效果的下游细胞过程的候选途径。我们还讨论了基于途径的多基因和全基因组方法在确定参与非小细胞肺癌临床结局的遗传因素中的应用。总的来说,目前的研究表明,每个个体多态性对临床结局的影响都很小,这表明需要更全面的方法,将多基因、表型、流行病学和临床变量结合起来,以预测接受铂类化疗的非小细胞肺癌患者的预后。