ATM regulation of IL-8 links oxidative stress to cancer cell migration and invasion

Elife. 2015 Jun 1:4:e07270. doi: 10.7554/eLife.07270.

Abstract

Ataxia-telangiectasia mutated (ATM) protein kinase regulates the DNA damage response (DDR) and is associated with cancer suppression. Here we report a cancer-promoting role for ATM. ATM depletion in metastatic cancer cells reduced cell migration and invasion. Transcription analyses identified a gene network, including the chemokine IL-8, regulated by ATM. IL-8 expression required ATM and was regulated by oxidative stress. IL-8 was validated as an ATM target by its ability to rescue cell migration and invasion defects in ATM-depleted cells. Finally, ATM-depletion in human breast cancer cells reduced lung tumors in a mouse xenograft model and clinical data validated IL-8 in lung metastasis. These findings provide insights into how ATM activation by oxidative stress regulates IL-8 to sustain cell migration and invasion in cancer cells to promote metastatic potential. Thus, in addition to well-established roles in tumor suppression, these findings identify a role for ATM in tumor progression.

Keywords: ATM; DNA damage; IL-8; ROS; cell biology; cell migration; chromosomes; genes; human; mouse.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Ataxia Telangiectasia Mutated Proteins / metabolism*
  • Blotting, Western
  • Breast Neoplasms / metabolism*
  • Cell Fractionation
  • Cell Movement / physiology*
  • Chromatin Immunoprecipitation
  • DNA Primers / genetics
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • Flow Cytometry
  • Gene Expression Regulation, Neoplastic / genetics
  • Gene Expression Regulation, Neoplastic / physiology*
  • Gene Regulatory Networks / genetics
  • Gene Regulatory Networks / physiology
  • Humans
  • Interleukin-8 / metabolism*
  • Luciferases
  • Lung Neoplasms / metabolism*
  • Lung Neoplasms / secondary
  • Mice
  • Microarray Analysis
  • Neoplasm Invasiveness / physiopathology*
  • Oxidative Stress / physiology*
  • Real-Time Polymerase Chain Reaction

Substances

  • DNA Primers
  • Interleukin-8
  • Luciferases
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.