Lascombe Isabelle, Clairotte Anne, Fauconnet Sylvie, Bernardini Stéphane, Wallerand Hervé, Kantelip Bernadette, Bittard Hugues
Tissue and Cell Biology Engineering, Besançon, France.
Clin Cancer Res. 2006 May 1;12(9):2780-7. doi: 10.1158/1078-0432.CCR-05-2387.
Loss of intercellular adhesion and increased cell motility promote tumor cell invasion and spreading. In bladder cancer, loss or reduced E-cadherin expression has been associated with poor survival, and aberrant expression of N-cadherin has been associated with the invasive phenotype of bladder carcinoma cells. The purpose of this study was to investigate whether N-cadherin expression was associated with the bladder tumor progression.
E-cadherin and N-cadherin expression was evaluated by immunohistochemistry in 101 tumors (pT1 and pT2-T3) and by reverse transcription-PCR analysis and immunohistochemistry in 28 other fresh frozen tumors (pT(a), pT1, and pT2-T3).
N-cadherin expression was absent in normal urothelium, appeared in stage pT1, and increased in pT2-pT3 tumors. In most cases, increased N-cadherin expression in invasive tumors was associated with loss of E-cadherin expression. Progression-free survival and multivariate analyses revealed that N-cadherin expression is an independent prognostic marker for pT1 tumor progression. Analysis of the 28 frozen tumors by immunohistochemistry and reverse transcription-PCR showed a good correlation between protein and gene expression in pT1 and pT2-T3 tumors. Interestingly, in pT(a) tumors, N-cadherin was not immunodetected, whereas mRNA was present in 50% of cases.
Regulatory defects in the N-cadherin promoter, abnormalities at the translational, or protein processing levels could explain the discrepancies between protein and mRNA expression. Most importantly, this study identified N-cadherin as a novel prognostic marker of progression in superficial urothelial tumors. Clearly, N-cadherin acts in an invasive mode in bladder cancer, but whether it has a primary role in urothelial neoplastic progression has yet to be investigated.
细胞间黏附丧失和细胞运动性增加促进肿瘤细胞侵袭和扩散。在膀胱癌中,E-钙黏蛋白表达缺失或降低与生存率低相关,而N-钙黏蛋白的异常表达与膀胱癌细胞的侵袭表型相关。本研究的目的是调查N-钙黏蛋白表达是否与膀胱肿瘤进展相关。
通过免疫组织化学评估101例肿瘤(pT1和pT2-T3)中E-钙黏蛋白和N-钙黏蛋白的表达,并通过逆转录-聚合酶链反应分析和免疫组织化学评估另外28例新鲜冷冻肿瘤(pT(a)、pT1和pT2-T3)中二者的表达。
正常尿路上皮中不存在N-钙黏蛋白表达,在pT1期出现,并在pT2-pT3期肿瘤中增加。在大多数情况下,侵袭性肿瘤中N-钙黏蛋白表达增加与E-钙黏蛋白表达缺失相关。无进展生存期和多变量分析显示,N-钙黏蛋白表达是pT1期肿瘤进展的独立预后标志物。通过免疫组织化学和逆转录-聚合酶链反应对28例冷冻肿瘤进行分析,结果显示pT1和pT2-T3期肿瘤中蛋白质和基因表达之间具有良好的相关性。有趣的是,在pT(a)期肿瘤中,未检测到N-钙黏蛋白免疫反应性,而50%的病例中存在mRNA。
N-钙黏蛋白启动子的调控缺陷、翻译或蛋白质加工水平的异常可以解释蛋白质和mRNA表达之间的差异。最重要的是,本研究确定N-钙黏蛋白是浅表性尿路上皮肿瘤进展的一种新的预后标志物。显然,N-钙黏蛋白在膀胱癌中以侵袭模式发挥作用,但其在尿路上皮肿瘤进展中是否起主要作用还有待研究。