ARF Confers a Context-Dependent Response to Chemotherapy in Muscle-Invasive Bladder Cancer

Cancer Res. 2017 Feb 15;77(4):1035-1046. doi: 10.1158/0008-5472.CAN-16-2621. Epub 2017 Jan 12.

Abstract

Muscle-invasive bladder cancer (MIBC) generally responds poorly to treatment and tends to exhibit significant mortality. Here we show that expression of the tumor suppressor p14ARF (ARF) is upregulated in aggressive subtypes of MIBC. Accumulation of ARF in the nucleolus is associated with poor outcome and attenuated response to chemotherapy. In both genetically engineered mouse models and murine xenograft models of human MIBC, we demonstrate that tumors expressing ARF failed to respond to treatment with the platinum-based chemotherapy agent cisplatin. Resistance was mediated in part by the integrin-binding protein ITGB3BP (CENPR) and reflected ARF-dependent impairment of protein translation, which was exaggerated by drug treatment. Overall, our results highlight a context-dependent role for ARF in modulating the drug response of bladder cancer. Cancer Res; 77(4); 1035-46. ©2017 AACR.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Cell Line, Tumor
  • Cisplatin / therapeutic use
  • DNA Damage
  • Drug Resistance, Neoplasm
  • Female
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Middle Aged
  • Neoplasm Invasiveness
  • Nuclear Proteins / physiology
  • Tumor Suppressor Protein p14ARF / analysis
  • Tumor Suppressor Protein p14ARF / physiology*
  • Tumor Suppressor Protein p53 / physiology
  • Urinary Bladder Neoplasms / drug therapy*
  • Urinary Bladder Neoplasms / pathology
  • Xenograft Model Antitumor Assays

Substances

  • ITGB3BP protein, human
  • Nuclear Proteins
  • Tumor Suppressor Protein p14ARF
  • Tumor Suppressor Protein p53
  • Cisplatin