Molecular classification of urothelial carcinoma: global mRNA classification versus tumour-cell phenotype classification

被引:270
作者
Sjodahl, Gottfrid [1 ]
Eriksson, Pontus [2 ]
Liedberg, Fredrik [1 ]
Hoglund, Mattias [2 ]
机构
[1] Lund Univ, Skane Univ Hosp, Div Urol Res, Dept Translat Med, Malmo, Sweden
[2] Lund Univ, Div Oncol & Pathol, Dept Clin Sci, Lund, Sweden
基金
瑞典研究理事会;
关键词
bladder cancer; molecular classification; tumour-cell phenotypes; pseudo-differentiation; BLADDER-CANCER; GENE; EXPRESSION; SUBTYPES; DIFFERENTIATION; IDENTIFICATION; PATHWAYS; TAXONOMY;
D O I
10.1002/path.4886
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Global mRNA expression analysis is efficient for phenotypic profiling of tumours, and has been used to define molecular subtypes for almost every major tumour type. A key limitation is that most tumours are communities of both tumour and non-tumour cells. This problem is particularly pertinent for analysis of advanced invasive tumours, which are known to induce major changes and responses in both the tumour and the surrounding tissue. To identify bladder cancer tumour-cell phenotypes and compare classification by tumour-cell phenotype with classification by global gene expression analysis, we analysed 307 advanced bladder cancers (cystectomized) both by genome gene expression analysis and by immunohistochemistry with antibodies for 28 proteins. According to systematic analysis of gene and protein expression data, focusing on key molecular processes, we describe five tumour-cell phenotypes of advanced urothelial carcinoma: urothelial-like, genomically unstable, basal/SCC-like, mesenchymal-like, and small-cell/neuroendocrine-like. We provide molecular pathological definitions for each subtype. Tumours expressing urothelial differentiation factors show inconsistent and abnormal protein expression of terminal differentiation markers, suggesting pseudo-differentiation. Cancers with different tumour-cell phenotypes may co-cluster (converge), and cases with identical tumour-cell phenotypes may cluster apart (diverge), in global mRNA analyses. This divergence/convergence suggests that broad global commonalities related to the invasive process may exist between muscle-invasive tumours regardless of specific tumour-cell phenotype. Hence, there is a systematic disagreement in subtype classification determined by global mRNA profiling and by immunohistochemical profiling at the tumour-cell level. We suggest that a combination of molecular pathology (tumour-cell phenotype) and global mRNA profiling (context) is required for adequate subtype classification of muscle-invasive bladder cancer. (C) 2017 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.
引用
收藏
页码:113 / 125
页数:13
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