Stepwise molecular mechanisms responsible for chemoresistance in bladder cancer cells

Cited 8 time in scopus
Metadata Downloads
Title
Stepwise molecular mechanisms responsible for chemoresistance in bladder cancer cells
Author(s)
J Y Mun; Seung Woo Baek; M S Jeong; In Hwan Jang; S R Lee; J Y You; J A Kim; G E Yang; Y H Choi; T N Kim; In-Sun Chu; S H Leem
Bibliographic Citation
Cell Death Discovery, vol. 8, pp. 450-450
Publication Year
2022
Abstract
Chemotherapy resistance is an obstacle to cancer therapy and is considered a major cause of recurrence. Thus, understanding the mechanisms of chemoresistance is critical to improving the prognosis of patients. Here, we have established a stepwise gemcitabine-resistant T24 bladder cancer cell line to understand the molecular mechanisms of chemoresistance within cancer cells. The characteristics of the stepwise chemoresistance cell line were divided into 4 phases (parental, early, intermediate, and late phases). These four phase cells showed increasingly aggressive phenotypes in vitro and in vivo experiments with increasing phases and revealed the molecular properties of the biological process from parent cells to phased gemcitabine-resistant cell line (GRC). Taken together, through the analysis of gene expression profile data, we have characterized gene set of each phase indicating the response to anticancer drug treatment. Specifically, we identified a multigene signature (23 genes including GATA3, APOBEC3G, NT5E, MYC, STC1, FOXD1, SMAD9) and developed a chemoresistance score consisting of that could predict eventual responsiveness to gemcitabine treatment. Our data will contribute to predicting chemoresistance and improving the prognosis of bladder cancer patients.
ISSN
2058-7716
Publisher
Springer-Nature Pub Group
Full Text Link
http://dx.doi.org/10.1038/s41420-022-01242-8
Type
Article
Appears in Collections:
Division of A.I. & Biomedical Research > Metabolic Regulation Research Center > 1. Journal Articles
Files in This Item:
  • There are no files associated with this item.


Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.