Assessment of Luminal and Basal Phenotypes in Bladder Cancer

Charles C. Guo(The University of Texas MD Anderson Cancer Center), Jolanta Bondaruk(The University of Texas MD Anderson Cancer Center), Hui Yao(The University of Texas MD Anderson Cancer Center), Ziqiao Wang(The University of Texas MD Anderson Cancer Center), Li Zhang(University of Cincinnati), Sangkyou Lee(The University of Texas MD Anderson Cancer Center), June-Goo Lee(The University of Texas MD Anderson Cancer Center), David Cogdell(The University of Texas MD Anderson Cancer Center), Miao Zhang(The University of Texas MD Anderson Cancer Center), Guoliang Yang(The University of Texas MD Anderson Cancer Center), Vipulkumar Dadhania(The University of Texas MD Anderson Cancer Center), Woonyoung Choi(Johns Hopkins University), Peng Wei(The University of Texas MD Anderson Cancer Center), Jianjun Gao(The University of Texas MD Anderson Cancer Center), Dan Theodorescu(Cedars-Sinai Medical Center), Christopher J. Logothetis(The University of Texas MD Anderson Cancer Center), Colin P. Dinney(The University of Texas MD Anderson Cancer Center), Marek Kimmel(Rice University), John N. Weinstein(The University of Texas MD Anderson Cancer Center), David J. McConkey(Johns Hopkins University), Bogdan Czerniak(The University of Texas MD Anderson Cancer Center)
Scientific Reports
June 16, 2020
Cited by 171Open Access
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Abstract

Genomic profiling studies have demonstrated that bladder cancer can be divided into two molecular subtypes referred to as luminal and basal with distinct clinical behaviors and sensitivities to frontline chemotherapy. We analyzed the mRNA expressions of signature luminal and basal genes in bladder cancer tumor samples from publicly available and MD Anderson Cancer Center cohorts. We developed a quantitative classifier referred to as basal to luminal transition (BLT) score which identified the molecular subtypes of bladder cancer with 80-94% sensitivity and 83-93% specificity. In order to facilitate molecular subtyping of bladder cancer in primary care centers, we analyzed the protein expressions of signature luminal (GATA3) and basal (KRT5/6) markers by immunohistochemistry, which identified molecular subtypes in over 80% of the cases. In conclusion, we provide a tool for assessment of molecular subtypes of bladder cancer in routine clinical practice.


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