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Common cancer stem cell gene variants predict colon cancer recurrence.

机译:常见的癌症干细胞基因变异预测结肠癌的复发。

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PURPOSE: Recent evidence suggests that cancer stem cells (CSC) are responsible for key elements of colon cancer progression and recurrence. Germline variants in CSC genes may result in altered gene function and/or activity, thereby causing interindividual differences in a patient's tumor recurrence capacity and chemoresistance. We investigated germline polymorphisms in a comprehensive panel of CSC genes to predict time to tumor recurrence (TTR) in patients with stage III and high-risk stage II colon cancer. EXPERIMENTAL DESIGN: A total of 234 patients treated with 5-fluorouracil-based chemotherapy at the University of Southern California were included in this study. Whole blood samples were analyzed for germline polymorphisms in genes that have been previously associated with colon CSC (CD44, Prominin-1, DPP4, EpCAM, ALCAM, Msi-1, ITGB1, CD24, LGR5, and ALDH1A1) by PCR-RFLP or direct DNA-sequencing. RESULTS: The minor alleles of CD44 rs8193 C>T, ALCAM rs1157 G>A, and LGR5 rs17109924 T>C were significantly associated with increased TTR (9.4 vs. 5.4 years; HR, 0.51; 95% CI: 0.35-0.93; P = 0.022; 11.3 vs. 5.7 years; HR, 0.56; 95% CI: 0.33-0.94; P = 0.024, and 10.7 vs. 5.7 years; HR, 0.33; 95% CI: 0.12-0.90; P = 0.023, respectively) and remained significant in the multivariate analysis stratified by ethnicity. In recursive partitioning, a specific gene variant profile including LGR5 rs17109924, CD44 rs8193, and ALDH1A1 rs1342024 represented a high-risk subgroup with a median TTR of 1.7 years (HR, 6.71, 95% CI: 2.71-16.63, P < 0.001). CONCLUSION: This is the first study identifying common germline variants in colon CSC genes as independent prognostic markers for stage III and high-risk stage II colon cancer patients. Clin Cancer Res; 17(21); 6934-43. (c)2011 AACR.
机译:目的:最近的证据表明,癌症干细胞(CSC)是结肠癌进展和复发的关键因素。 CSC基因中的种系变异可能导致基因功能和/或活性改变,从而导致患者的肿瘤复发能力和化学耐药性出现个体差异。我们调查了全面的CSC基因组中的种系多态性,以预测III期和高危II期结肠癌患者的肿瘤复发时间(TTR)。实验设计:这项研究共包括234名在南加州大学接受基于5氟尿嘧啶的化学疗法治疗的患者。通过PCR-RFLP或直接分析全血样品中先前与结肠CSC(CD44,Prominin-1,DPP4,EpCAM,ALCAM,Msi-1,ITGB1,CD24,LGR5和ALDH1A1)相关的基因的种系多态性DNA测序。结果:CD44 rs8193 C> T,ALCAM rs1157 G> A和LGR5 rs17109924 T> C的次要等位基因与TTR增加显着相关(9.4 vs. 5.4岁; HR,0.51; 95%CI:0.35-0.93; P = 0.022; 11.3 vs. 5.7年; HR,0.56; 95%CI:0.33-0.94; P = 0.024; and 10.7 vs. 5.7年; HR,0.33; 95%CI:0.12-0.90; P = 0.023)并且在按族裔分层的多变量分析中仍然很重要。在递归分区中,包括LGR5 rs17109924,CD44 rs8193和ALDH1A1 rs1342024的特定基因变异谱代表高风险亚组,中位TTR为1.7年(HR,6.71、95%CI:2.71-16.63,P <0.001)。结论:这是第一项鉴定结肠CSC基因中常见种系变异体作为III期和高危II期结肠癌患者独立预后标志物的研究。临床癌症研究; 17(21); 6934-43。 (c)2011年美国机修协会。

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