Bläsius Felix Marius, Meller Sebastian, Stephan Carsten, Jung Klaus, Ellinger Jörg, Glocker Michael O, Thiesen Hans-Jürgen, Tolkach Yuri, Kristiansen Glen
Institute of Pathology, University Hospital Bonn, Bonn, Germany.
Clinic of Urology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Oncotarget. 2017 Aug 24;8(43):75076-75086. doi: 10.18632/oncotarget.20507. eCollection 2017 Sep 26.
Reduced expression of Cadherin-Related Family Member 5 (CDHR5) was recently found implied in carcinogenesis of colon cancer, but its role in other tumors is unknown. We aimed to analyze the expression of CDHR5 in different subtypes of renal cell carcinoma. CDHR5 expression was immunohistochemically examined using tissue micro arrays (TMAs) covering 279 patients with primary renal cell carcinoma. Additionally, expression data from the TCGA (The Cancer Genome Atlas) of an independent cohort of 489 clear-cell RCC cases was evaluated. CDHR5 protein expression was found in 74.9% of cases, with higher levels seen in clear cell and papillary RCC. In the univariate analysis CDHR5 expression was significantly associated with a longer overall survival of RCC patients at the protein (p = 0.026, HR = 0.56) and transcript levels (TCGA-cohort: p = 0.0002, HR = 0.55). Importantly, differences in survival times were confirmed independently in multivariate analyses in a model with common clinicopathological variables at the transcript level (p = 0.0097, HR = 0.65). Investigation of the putative functional role of CDHR5 using TCGA data and Enrichment analysis for Gene Ontology and Pathways revealed associations with many metabolic and some tumor growth-associated processes and pathways. CDHR5 expression appears to be a promising and new independent prognostic biomarker in renal cell carcinoma.
最近发现钙黏蛋白相关家族成员5(CDHR5)表达降低与结肠癌的致癌作用有关,但其在其他肿瘤中的作用尚不清楚。我们旨在分析CDHR5在不同亚型肾细胞癌中的表达情况。使用覆盖279例原发性肾细胞癌患者的组织微阵列(TMA)对CDHR5表达进行免疫组织化学检测。此外,还评估了来自489例透明细胞肾细胞癌独立队列的癌症基因组图谱(TCGA)的表达数据。在74.9%的病例中发现了CDHR5蛋白表达,在透明细胞和乳头状肾细胞癌中表达水平更高。在单变量分析中,CDHR5表达与肾细胞癌患者在蛋白水平(p = 0.026,HR = 0.56)和转录水平(TCGA队列:p = 0.0002,HR = 0.55)的较长总生存期显著相关。重要的是,在转录水平上,在包含常见临床病理变量的多变量分析模型中独立证实了生存时间的差异(p = 0.0097,HR = 0.65)。使用TCGA数据以及基因本体和通路富集分析对CDHR5的假定功能作用进行研究,发现其与许多代谢过程以及一些肿瘤生长相关过程和通路有关。CDHR5表达似乎是肾细胞癌中一个有前景的新的独立预后生物标志物。