Published online Aug 26, 2016. doi: 10.4252/wjsc.v8.i8.260
Peer-review started: March 22, 2016
First decision: April 20, 2016
Revised: April 25, 2016
Accepted: June 27, 2016
Article in press: June 29, 2016
Published online: August 26, 2016
Processing time: 153 Days and 16.1 Hours
Core tip: A subset of bladder cancer cells, known as urothelial cancer stem cells, have abilities to self-renew, generate tumor heterogeneity via differentiation, and are actually responsible for tumor relapse and metastasis formation. Delineating the mechanistic complexity between epithelial plasticity and cancer stemness in malignant transformation of urothelial carcinoma provides the basis for designing rational therapies. Differentiation and elimination therapies targeting the potential biomarkers could prove to be clinically beneficial by suppressing the cancer stemness and inhibiting epithelial-to-mesenchymal transition phenotype and would provide novel opportunities for targeted therapeutic approaches in the clinical management of patients.
