Research Papers:

Mitochondrial DNA content in breast cancer: Impact on in vitro and in vivo phenotype and patient prognosis

Marjolein J.A. Weerts _, Anieta M. Sieuwerts, Marcel Smid, Maxime P. Look, John A. Foekens, Stefan Sleijfer and John W.M. Martens

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Oncotarget. 2016; 7:29166-29176. https://doi.org/10.18632/oncotarget.8688

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Marjolein J.A. Weerts1, Anieta M. Sieuwerts1, Marcel Smid1, Maxime P. Look1, John A. Foekens1, Stefan Sleijfer1, John W.M. Martens1

1Department of Medical Oncology and Cancer Genomics, Erasmus MC Cancer Institute, Erasmus University Medical Center, Rotterdam, The Netherlands

Correspondence to:

Marjolein J.A. Weerts, email: [email protected]

Keywords: breast cancer, mitochondrial DNA, mtDNA content, epithelial-to-mesenchymal transition, distant metastasis

Received: November 27, 2015     Accepted: March 28, 2016     Published: April 11, 2016


Reduced mitochondrial DNA (mtDNA) content in breast cancer cell lines has been associated with transition towards a mesenchymal phenotype, but its clinical consequences concerning breast cancer dissemination remain unidentified. Here, we aimed to clarify the link between mtDNA content and a mesenchymal phenotype and its relation to prognosis of breast cancer patients. We analyzed mtDNA content in 42 breast cancer cell lines and 207 primary breast tumor specimens using a combination of quantitative PCR and array-based copy number analysis. By associating mtDNA content with expression levels of genes involved in epithelial-to-mesenchymal transition (EMT) and with the intrinsic breast cancer subtypes, we could not identify a relation between low mtDNA content and mesenchymal properties in the breast cancer cell lines or in the primary breast tumors. In addition, we explored the relation between mtDNA content and prognosis in our cohort of primary breast tumor specimens that originated from patients with lymph node-negative disease who did not receive any (neo)adjuvant systemic therapy. When patients were divided based on the tumor quartile levels of mtDNA content, those in the lowest quarter (≤ 350 mtDNA molecules per cell) showed a poorer 10-year distant metastasis-free survival than patients with > 350 mtDNA molecules per cell (HR 0.50 [95% CI 0.29–0.87], P = 0.015). The poor prognosis was independent of established clinicopathological markers (HR 0.54 [95% CI 0.30–0.97], P = 0.038). We conclude that, despite a lack of evidence between mtDNA content and EMT, low mtDNA content might provide meaningful prognostic value for distant metastasis in breast cancer.

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