Author:
Guo Charles C.,Bondaruk Jolanta,Yao Hui,Wang Ziqiao,Zhang Li,Lee Sangkyou,Lee June-Goo,Cogdell David,Zhang Miao,Yang Guoliang,Dadhania Vipulkumar,Choi Woonyoung,Wei Peng,Gao Jianjun,Theodorescu Dan,Logothetis Christopher,Dinney Colin,Kimmel Marek,Weinstein John N.,McConkey David J.,Czerniak Bogdan
Abstract
AbstractGenomic 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.
Publisher
Springer Science and Business Media LLC