Identification of the interferon-inducible double-stranded RNA-dependent protein kinase as a regulator of cellular response to bulky adducts

Cancer Res. 2000 Dec 15;60(24):6800-4.

Abstract

The double-stranded RNA-dependent protein kinase PKR plays a central role in IFN-mediated antiviral response. The ability of PKR mutants to transform rodent fibroblasts led to the hypothesis that PKR acts as a tumor suppressor. Recent studies have identified an expanding network of PKR signaling partners, including signal transducers and activators of transcription 1 (STAT1), p53, and IkappaB-kinase. Here we demonstrate that PKR is involved in the cellular response to genotoxic stress. PKR-deficient mouse-embryonic fibroblasts (PKR-/-) are hypersensitive to bulky adduct DNA damage caused by cisplatin, melphalan, and UV radiation but not to other DNA-damaging agents such as Adriamycin. PKR-deficient cells are highly susceptible to cisplatin-induced apoptosis. They demonstrate retarded cisplatin adduct removal kinetics. Most strikingly, PKR localizes to the nucleus rapidly upon cisplatin treatment. Restoration of PKR in PKR-/- cells results in resistance to cisplatin and enhanced cell capacity to remove cisplatin DNA adducts. We conclude that PKR has a function in the regulation of cellular response to bulky adduct-inducing agents, possibly by modulating DNA repair mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents, Alkylating / pharmacokinetics
  • Apoptosis
  • Cisplatin / pharmacokinetics
  • DNA / drug effects
  • DNA / radiation effects
  • DNA Adducts / metabolism*
  • DNA Repair
  • Dose-Response Relationship, Drug
  • Doxorubicin / pharmacokinetics
  • Fibroblasts / metabolism
  • Fibroblasts / pathology
  • Genotype
  • Humans
  • Immunoblotting
  • Immunohistochemistry
  • Interferons / metabolism*
  • Kinetics
  • Melphalan / pharmacokinetics
  • Mice
  • Microscopy, Fluorescence
  • RNA, Double-Stranded / metabolism*
  • Retroviridae / genetics
  • Signal Transduction
  • Time Factors
  • Tumor Cells, Cultured
  • Ultraviolet Rays
  • eIF-2 Kinase / genetics
  • eIF-2 Kinase / metabolism*
  • eIF-2 Kinase / physiology*

Substances

  • Antineoplastic Agents
  • Antineoplastic Agents, Alkylating
  • DNA Adducts
  • RNA, Double-Stranded
  • Doxorubicin
  • DNA
  • Interferons
  • eIF-2 Kinase
  • Cisplatin
  • Melphalan