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Involvement of metformin and AMPK in the radioresponse and prognosis of luminal versus basal-like breast cancer treated with radiotherapy

Zhang, Yimin; Storr, Sarah J.; Johnson, Kerstie; Green, Andrew R.; Rakha, Emad A.; Ellis, Ian O.; Morgan, David A.L.; Martin, Stewart G.

Involvement of metformin and AMPK in the radioresponse and prognosis of luminal versus basal-like breast cancer treated with radiotherapy Thumbnail


Authors

Yimin Zhang

Profile image of SARAH STORR

SARAH STORR sarah.storr@nottingham.ac.uk
Assistant Professor

Kerstie Johnson

EMAD RAKHA Emad.Rakha@nottingham.ac.uk
Professor of Breast Cancer Pathology

Ian O. Ellis

David A.L. Morgan

STEWART MARTIN STEWART.MARTIN@NOTTINGHAM.AC.UK
Professor of Cancer and Radiation Biology



Abstract

Metformin is under evaluation as a potential anticancer agent. Expression of total and phospho(Thr172)-adenosine monophosphate-activated kinase-α (AMPKα and pAMPKα(Thr172) respectively), a main metformin target, was examined in radiotherapy treated breast cancers and metformin’s ability to modulate Trx system expression and breast cancer radiosensitivity evaluated in vitro.

AMPKα and pAMPKα(Thr172) expression was assessed using a discovery (n=166) and validation cohort (n=609). Metformin’s role in regulating radioresponse, and Trx family expression, was examined via clonogenic assays and Western blots. Intracellular reactive oxygen species (ROS) levels, cell cycle progression and apoptosis were assessed by flow cytometry.

High AMPKα expression associated with improved local recurrence-free (P=0.019), relapse-free (P=0.016) and breast cancer-specific survival (P=0.000065) and was, from multivariate analysis, an independent prognostic factor from the discovery cohort. From the validation cases AMPKα expression associated with relapse-free and breast cancer-specific survival in luminal breast cancers. Metformin substantially increased radiosensitivity, intracellular ROS levels and reduced Trx expression, in luminal breast cancer cells, but had little effect on basal phenotype cells.

In conclusion, high AMPKα expression associates with improved prognosis, especially in luminal breast cancer. Metformin preferentially radiosensitises luminal breast cancer cells, potentially due to alterations to intracellular ROS levels via modulation of Trx family protein expression.

Journal Article Type Article
Acceptance Date Nov 4, 2014
Publication Date Nov 4, 2014
Deposit Date Aug 14, 2018
Publicly Available Date Oct 19, 2018
Electronic ISSN 1949-2553
Publisher Impact Journals
Peer Reviewed Peer Reviewed
Volume 5
Issue 24
DOI https://doi.org/10.18632/oncotarget.2683
Keywords metformin; AMPK; radiosensitivity; breast cancer; luminal phenotype
Public URL https://nottingham-repository.worktribe.com/output/1100826
Publisher URL http://www.oncotarget.com/index.php?journal=oncotarget&page=article&op=view&path[]=2683&path[]=5134
PMID 25427448

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