Deoxycytidine kinase expression underpins response to gemcitabine in bladder cancer.

ABSTRACT:

Purpose

In a recent phase II clinical trial, low-dose (100 mg/m(2)) gemcitabine showed promise as a radiosensitizer in bladder cancer, but underlying mechanisms lack elucidation. Here, we investigated the mechanism of radiosensitization by low-dose gemcitabine in bladder cancer cell lines.

Experimental design

Four bladder cancer cell lines were screened for radiosensitization by low-dose gemcitabine using clonogenic assay, and gemcitabine-resistant RT112gem and CALgem cells created by exposure to increasing gemcitabine doses. Four key gemcitabine-regulatory genes were knocked down by transient siRNA. Nude mice carrying CALgem subcutaneous xenografts were exposed to 100 mg/kg gemcitabine ± ionizing radiation (IR) and response assessed by tumor growth delay.

Results

Gem

SUBMITTER: Kerr M 

PROVIDER: S-EPMC4216732 | biostudies-literature | 2014 Nov

REPOSITORIES: biostudies-literature