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鉴定 Claudin-4 和 E-钙黏蛋白评分预测乳腺癌的预后。

Identification of a claudin-4 and E-cadherin score to predict prognosis in breast cancer.

机构信息

Second Department of Pathology, Semmelweis University, Budapest, Hungary.

出版信息

Cancer Sci. 2011 Dec;102(12):2248-54. doi: 10.1111/j.1349-7006.2011.02085.x. Epub 2011 Oct 12.

DOI:10.1111/j.1349-7006.2011.02085.x
PMID:21883696
Abstract

The elevated expression of claudins (CLDN) and E-cadherin (CDH-1) was found to correlate with poor prognostic features. Our aim was to perform a comprehensive analysis to assess their potential to predict prognosis in breast cancer. The expression of CLDN-1, -3-5, -7, -8, -10, -15, -18, and E-cadherin at the mRNA level was evaluated in correlation with survival in datasets containing expression measurements of 1809 breast cancer patients. The breast cancer tissues of 197 patients were evaluated with tissue microarray technique and immunohistochemical method for CLDN-1-5, -7, and E-cadherin protein expression. An additional validation set of 387 patients was used to test the accuracy of the resulting prognostic score. Based on the bioinformatic screening of publicly-available datasets, the metagene of CLDN-3, -4, -7, and E-cadherin was shown to have the most powerful predictive power in the survival analyses. An immunohistochemical protein profile consisting of CLDN-2, -4, and E-cadherin was able to predict outcome in the most effective manner in the training set. Combining the overlapping members of the above two methods resulted in the claudin-4 and E-cadherin score (CURIO), which was able to accurately predict relapse-free survival in the validation cohort (P = 0.029). The multivariate analysis, including clinicopathological variables and the CURIO, showed that the latter kept its predictive power (P = 0.040). Furthermore, the CURIO was able to further refine prognosis, separating good versus poor prognosis subgroups in luminal A, luminal B, and triple-negative breast cancer intrinsic subtypes. In breast cancer, the CURIO provides additional prognostic information besides the routinely utilized diagnostic approaches and factors.

摘要

CLDN(紧密连接蛋白)和 E-cadherin(E-钙黏蛋白)的高表达与不良预后特征相关。我们的目的是进行全面分析,以评估它们在乳腺癌预后预测中的潜力。在包含 1809 例乳腺癌患者表达测量数据的数据集 中,评估了 CLDN-1、-3-5、-7、-8、-10、-15、-18 和 E-cadherin 的 mRNA 水平表达与生存的相关性。采用组织微阵列技术和免疫组织化学方法,对 197 例乳腺癌患者的 CLDN-1-5、-7 和 E-cadherin 蛋白表达进行了评估。还使用了 387 例患者的验证集来测试所得预后评分的准确性。基于公开数据集的生物信息学筛选,CLDN-3、-4、-7 和 E-cadherin 的 metagene 在生存分析中显示出最强的预测能力。由 CLDN-2、-4 和 E-cadherin 组成的免疫组织化学蛋白谱在训练集中能够以最有效的方式预测结局。将上述两种方法的重叠成员结合起来,产生了紧密连接蛋白-4 和 E-cadherin 评分(CURIO),它能够在验证队列中准确预测无复发生存率(P=0.029)。包括临床病理变量和 CURIO 的多变量分析表明,后者保持其预测能力(P=0.040)。此外,CURIO 能够进一步细化预后,在管腔 A、管腔 B 和三阴性乳腺癌内在亚型中,将良好预后与不良预后亚组分开。在乳腺癌中,CURIO 提供了常规诊断方法和因素之外的额外预后信息。

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