Department of Pathology, Seoul National University College of Medicine, Seoul 03080, Korea.
Seoul National University Biomedical Informatics (SNUBI), Division of Biomedical Informatics and Systems Biomedical Informatics National Core Research Center, Seoul National University College of Medicine, Seoul 03080, Korea.
Int J Mol Sci. 2019 Jan 29;20(3):570. doi: 10.3390/ijms20030570.
Immunohistochemical (IHC) staining for CK5/6 and CK20 was reported to be correlated with the prognosis of early urothelial carcinoma in a way contrary to that of advanced tumors for unknown reasons. We aimed to characterize the gene expression profiles of subgroups of non-muscle-invasive papillary high-grade upper tract urothelial carcinoma (UTUC) classified by CK5/6 and CK20 expression levels: group 1 (CK5/6-high/CK20-low), group 2 (CK5/6-high/CK20-high), and group 3 (CK5/6-low/CK20-high). Expression of group 3 was predictive of worse prognosis of non-muscle-invasive papillary high-grade UTUC. Transcriptional analysis revealed 308 differentially expressed genes across the subgroups. Functional analyses of the genes identified cell adhesion as a common process differentially enriched in group 3 compared to the other groups, which could explain its high-risk phenotype. Late cell cycle/proliferation signatures were also enriched in group 3 and in some of the other groups, which may be used as a prognostic biomarker complementary to CK5/6 and CK20. Group 2, characterized by low levels of genes associated with mitogen-activated protein kinase and tumor necrosis factor signaling pathways, was hypothesized to represent the least cancerous subtype considering its normal urothelium-like IHC pattern. This study would facilitate the application of easily accessible prognostic biomarkers in practice.
免疫组织化学(IHC)染色 CK5/6 和 CK20 的结果与早期尿路上皮癌的预后相关,这与晚期肿瘤的结果相反,但原因尚不清楚。我们旨在通过 CK5/6 和 CK20 表达水平对非肌肉浸润性高级别乳头状上尿路尿路上皮癌(UTUC)的亚组进行基因表达谱特征分析:第 1 组(CK5/6 高/CK20 低),第 2 组(CK5/6 高/CK20 高)和第 3 组(CK5/6 低/CK20 高)。第 3 组的表达预示着非肌肉浸润性高级别乳头状 UTUC 的预后较差。转录分析显示,308 个基因在亚组间存在差异表达。对基因的功能分析表明,与其他亚组相比,第 3 组的细胞黏附是一个共同的差异富集过程,这可以解释其高风险表型。晚期细胞周期/增殖特征也在第 3 组和其他一些亚组中富集,这可能作为 CK5/6 和 CK20 的补充预后生物标志物。第 2 组的特征是与丝裂原活化蛋白激酶和肿瘤坏死因子信号通路相关的基因水平较低,考虑到其正常尿路上皮样 IHC 模式,假设其为最具癌症特征的亚型。这项研究将有助于在实践中应用易于获得的预后生物标志物。