Research Papers:
Association of miR-548c-5p, miR-7-5p, miR-210-3p, miR-128-3p with recurrence in systemically untreated breast cancer
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Abstract
Ines Block1, Mark Burton1,2, Kristina P. Sørensen1, Lars Andersen1,2, Martin J. Larsen1,2, Martin Bak3, Søren Cold4, Mads Thomassen1,2, Qihua Tan2,5 and Torben A. Kruse1,2
1Department of Clinical Genetics, Odense University Hospital, Odense, Denmark
2Human Genetics, Department of Clinical Research, University of Southern Denmark, Odense, Denmark
3Department of Pathology, Odense University Hospital, Odense, Denmark
4Department of Oncology, Odense University Hospital, Odense, Denmark
5Epidemiology, Department of Public Health, University of Southern Denmark, Odense, Denmark
Correspondence to:
Ines Block, email: [email protected]
Keywords: low-risk breast cancer; microRNA; prognosis; lymph node negative; estrogen receptor positive
Received: September 24, 2017 Accepted: January 02, 2018 Published: January 09, 2018
ABSTRACT
Current prognostic markers allocate the majority of lymph node (LN) negative and estrogen receptor (ER) positive breast cancer patients into the high-risk group. Accordingly, most patients receive systemic treatments although approximately 40% of these patients may have been cured by surgery and radiotherapy alone. Two studies identified seven prognostic microRNAs in systemically untreated, LN negative and ER positive breast cancer patients which may allow more precise patient classification. However, six of the seven microRNAs were analyzed in both studies but only found to be prognostic in one study. To validate their prognostic potential, we analyzed microRNA expression in an independent cohort (n = 110) using a pair-matched study design minimizing dependence of classical markers. The expression of hsa-miR-548c-5p was significantly associated with abridged disease-free survival (hazard ratio [HR]:1.96, p = 0.027). Contradicting published results, high hsa-miR-516-3p expression was associated with favorable outcome (HR:0.29, p = 0.0068). The association is probably time-dependent indicating later relapse. Additionally, re-analysis of previously published expression data of two matching cohorts (n = 100, n = 255) supports an association of hsa-miR-128-3p with shortened disease-free survival (HR:2.48, p = 0.0033) and an upregulation of miR-7-5p (p = 0.0038; p = 0.039) and miR-210-3p (p = 0.031) in primary tumors of patients who experienced metastases. Further analysis may verify the prognostic potential of these microRNAs.
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