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

نویسندگان

  • Wei-Ta Chen
  • Nancy D Ebelt
  • Travis H Stracker
  • Blerta Xhemalce
  • Carla L Van Den Berg
  • Kyle M Miller
  • Joaquin M Espinosa
چکیده

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.

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عنوان ژورنال:

دوره 4  شماره 

صفحات  -

تاریخ انتشار 2015