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Prognostic significance of recurrent chromosomal aberrations detected by comparative genomic hybridization in sporadic colorectal cancer.

机译:通过比较基因组杂交检测散发性结直肠癌中复发性染色体畸变的预后意义。

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Colorectal carcinomas are characterized by frequent recurrent gains and losses of chromosomal material, especially gains of chromosome arms 20q and 13q, and losses of chromosome arms 18q and 4q. These may be important in the development and progression of colorectal carcinomas. Chromosomal aberrations detected by comparative genomic hybridization in 67 sporadic colorectal carcinomas were examined for their possible associations with patient survival. Dukes' stage, tumor DNA ploidy status, and TP53 genotype/phenotype were also examined for the same. Patients with losses of chromosomal arms 1p, 4q, 8p, 14q, or 18q or gain of chromosomal arm 20q had significantly shorter survival times than those without these aberrations (univariate relative risk 3.45, 2.71, 3.32, 3.26, 3.32, 3.91, respectively), as did patients with more than six chromosomal aberrations per tumor than those with fewer than six aberrations (univariate relative risk 3.26, P = 0.013). DNA aneuploidy and Dukes' stage C + D resulted in poor patient survival (univariate relative risk 3.58, 3.39, respectively). Dukes' stage C + D, 1p loss and 8p loss emerged as the only independent prognostic parameters (relative risk 3.22, 2.53, 2.45, respectively) when entered into multivariate survival analysis together with other significant parameters from univariate survival analysis. Loss of chromosome arm 1p, 4q, 8p, 14q, or 18q or gain of chromosome arm 20q thus results in shortened survival times in colorectal cancer patients. 1p loss and 8p loss were shown to be independent predictors of poor prognosis.
机译:大肠癌的特征是频繁反复获得和丢失染色体物质,尤其是染色体臂20q和13q的获得,以及染色体臂18q和4q的丢失。这些对于大肠癌的发生和发展可能是重要的。检查通过比较基因组杂交在67例散发性结直肠癌中检测到的染色体畸变与患者生存的可能关联。还检查了Dukes分期,肿瘤DNA倍性状态和TP53基因型/表型。染色体臂缺失1p,4q,8p,14q或18q或染色体臂缺失20q的患者的生存时间比没有这些畸变的患者显着更短(分别为相对风险3.45、2.71、3.32、3.26、3.32、3.91)与每个肿瘤的染色体畸变多于六个的患者相比,每个肿瘤的染色体畸变多于六个的患者(单因素相对危险度3.26,P = 0.013)。 DNA非整倍性和Dukes的C + D期导致患者生存不良(相对风险分别为3.58、3.39)。当进入多变量生存分析以及来自单变量生存分析的其他重要参数时,Dukes的C + D期,1p丢失和8p丢失是唯一的独立预后参数(相对风险分别为3.22、2.53、2.45)。染色体臂1p,4q,8p,14q或18q的丢失或染色体臂20q的获得因此导致大肠癌患者的生存时间缩短。 1p丢失和8p丢失是不良预后的独立预测因子。

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