Xing Jinliang, Wu Xifeng, Vaporciyan Ara A, Spitz Margaret R, Gu Jian
Department of Epidemiology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Cancer. 2008 Jun 15;112(12):2756-64. doi: 10.1002/cncr.23533.
The double-strand break (DSB) repair capacity has been implicated in the survival of patients in several cancer types. However, little is known about the prognostic importance of the key DSB repair genes-ataxia-telangiectasia mutated (ATM), DNA-dependent protein kinase catalytic subunit (DNA-PKcs), and the Ku heterodimeric regulatory complex 86-kD subunit (Ku80)-in nonsmall cell lung cancer (NSCLC). To address this issue, the authors determined the messenger RNA (mRNA) expression of these genes in patients NSCLC and assessed their prognostic relevance.
mRNA expression levels of ATM, DNA-PKcs, and Ku80 were measured in tumor and adjacent normal tissues from 140 patients with NSCLC by using quantitative real-time polymerase chain reaction analysis. Then, a Cox proportional hazards regression model and Kaplan-Meier plots were used to evaluate the association between the tumor:normal (T/N) expression ratios of the 3 genes and the overall survival rate and duration in patients with NSCLC.
mRNA expression of ATM and DNA-PKcs, but not of Ku80, was significantly higher in tumor tissues than in adjacent normal tissues (P=.003 and P<.001, respectively). The high T/N expression ratios of ATM and DNA-PKcs were associated significantly with a 1.82-fold increased risk of death (95% confidence interval, 1.05-2.70) and a 2.13-fold increased risk of death (95% confidence interval, 1.21-3.76), respectively. However, no significant association with risk was observed for Ku80. Kaplan-Meier analyses revealed that patients with high T/N expression ratios of ATM or DNA-PKcs had notably shorter median survival than patients with low ratios.
The current findings suggested that the T/N expression ratios of ATM and DNA-PKcs may be useful for identifying NSCLC patients with a poor prognosis who may benefit from more aggressive therapy.
双链断裂(DSB)修复能力与多种癌症类型患者的生存率有关。然而,对于关键的DSB修复基因——共济失调毛细血管扩张症突变基因(ATM)、DNA依赖蛋白激酶催化亚基(DNA-PKcs)以及Ku异源二聚体调节复合物86-kD亚基(Ku80)——在非小细胞肺癌(NSCLC)中的预后重要性,人们了解甚少。为解决这一问题,作者测定了这些基因在NSCLC患者中的信使核糖核酸(mRNA)表达,并评估了它们的预后相关性。
采用定量实时聚合酶链反应分析,测量了140例NSCLC患者肿瘤组织及相邻正常组织中ATM、DNA-PKcs和Ku80的mRNA表达水平。然后,使用Cox比例风险回归模型和Kaplan-Meier曲线来评估这3个基因的肿瘤与正常组织(T/N)表达比值与NSCLC患者总生存率及生存时间之间的关联。
肿瘤组织中ATM和DNA-PKcs的mRNA表达显著高于相邻正常组织(分别为P = 0.003和P < 0.001),而Ku80的mRNA表达无显著差异。ATM和DNA-PKcs的高T/N表达比值分别与死亡风险增加1.82倍(95%置信区间,1.05 - 2.70)和2.13倍(95%置信区间,1.21 - 3.76)显著相关。然而,未观察到Ku80与风险有显著关联。Kaplan-Meier分析显示,ATM或DNA-PKcs的T/N表达比值高的患者中位生存期明显短于比值低的患者。
目前的研究结果表明,ATM和DNA-PKcs的T/N表达比值可能有助于识别预后不良的NSCLC患者,这些患者可能从更积极的治疗中获益。