Circulating Micro-RNAs Predict the Risk of Recurrence in Triple-Negative Breast Cancer
- Jouni Kujala 1, Maria Tengström 2, Sami Heikkinen 3, Mari Taipale 3,4, Veli-Matti Kosma 1,5, Jaana M Hartikainen 1,6,7, Arto Mannermaa 1,5,7
- 1Institute of Clinical Medicine, Clinical Pathology and Forensic Medicine, University of Eastern Finland, FI-70211 Kuopio, Finland.
- 2Cancer Center, Department of Oncology, Kuopio University Hospital, FI-70029 Kuopio, Finland.
- 3Institute of Biomedicine, School of Medicine, University of Eastern Finland, FI-70211 Kuopio, Finland.
- 4A. I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, FI-70211 Kuopio, Finland.
- 5Biobank of Eastern Finland, Kuopio University Hospital, FI-70029 Kuopio, Finland.
- 6Genome Center of Eastern Finland, Institute of Clinical Medicine, University of Eastern Finland, FI-70211 Kuopio, Finland.
- 7Multidisciplinary Cancer Research Community (Cancer RC), University of Eastern Finland, FI-70211 Kuopio, Finland.
- 0Institute of Clinical Medicine, Clinical Pathology and Forensic Medicine, University of Eastern Finland, FI-70211 Kuopio, Finland.
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View abstract on PubMed
Summary
This summary is machine-generated.Triple-negative breast cancer (TNBC) recurrence risk can be assessed using circulating micro-RNAs (cmiRNAs) from liquid biopsies. Three specific cmiRNAs show potential as prognostic biomarkers for predicting TNBC recurrence and survival outcomes.
Area Of Science
- Oncology
- Molecular Biology
- Biomarker Discovery
Background
- Triple-negative breast cancer (TNBC) is an aggressive subtype characterized by high recurrence rates.
- Liquid biopsies offer a non-invasive method for detecting cancer biomarkers.
- Circulating micro-RNAs (cmiRNAs) are emerging as potential prognostic indicators in various cancers.
Purpose Of The Study
- To investigate the utility of serum cmiRNAs as prognostic biomarkers for TNBC recurrence.
- To compare cmiRNA expression profiles between recurrent and non-recurrent TNBC cases.
- To identify specific cmiRNAs associated with recurrence-free survival in TNBC.
Main Methods
- Serum samples from 14 recurrent and 19 non-recurrent TNBC patients were analyzed for cmiRNA sequencing.
- Differential expression analysis was performed to identify cmiRNAs associated with recurrence status.
- Multivariable survival analysis was used to assess the association of cmiRNAs with recurrence-free survival.
- Correlation analysis was conducted between serum and matched tumor cmiRNA expression profiles.
Main Results
- Ten differentially expressed (DE) cmiRNAs were identified between recurrent and non-recurrent TNBC cases.
- Three cmiRNAs (miR-21-5p, miR-16-5p, miR-26b-5p) were significantly associated with recurrence-free survival.
- Serum and matched tumor cmiRNA expression profiles showed a positive correlation.
- DE cmiRNAs were linked to cancer-related signaling pathways and improved recurrence risk prediction models.
Conclusions
- Recurrent and non-recurrent TNBC exhibit distinct serum cmiRNA expression profiles.
- Specific cmiRNAs, including miR-21-5p, miR-16-5p, and miR-26b-5p, can serve as prognostic biomarkers for TNBC recurrence risk.
- Serum cmiRNAs hold promise for non-invasive assessment and management of TNBC recurrence.
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