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Updated: Feb 3, 2026

Clinicopathological Analysis of miRNA Expression in Breast Cancer Tissues by Using miRNA In Situ Hybridization
Published on: June 7, 2016
miRNA and long non-coding RNA: molecular function and clinical value in breast and ovarian cancers
Konstantina Panoutsopoulou1, Margaritis Avgeris1, Andreas Scorilas1
1a Department of Biochemistry and Molecular Biology, Faculty of Biology , National and Kapodistrian University of Athens , Athens , Greece.
Introduction:
The elucidation of tumor molecular hallmarks and the identification of novel molecular markers are of first translational priority in breast and ovarian cancer research, aiming to support personalized disease treatment and monitoring decisions. Recent high-throughput studies have revealed that ~ 80% of the genome is transcribed into RNAs without protein-coding potential, namely non-coding RNAs (ncRNAs), challenging the concept of 'junk DNA'. Undoubtedly, microRNAs (miRNAs) and long non-coding RNAs (lncRNAs) represent the best-studied family classes, emerging as the most powerful gene-expression regulators at epigenetic, transcriptional and post-transcriptional levels. Areas covered: Cancer research has highlighted the active implication of ncRNAs, most notably of miRNAs and lncRNAs, in almost every aspect of the cancer cells' biology as well as their deregulated expression in both breast and ovarian tumors. In the present manuscript we discuss the existing knowledge regarding the involvement of miRNAs and lncRNAs in the molecular background of breast and ovarian malignancies, to highlight their clinical utility in improving disease management. Expert commentary: miRNAs and lncRNAs represent central mediators of cancer cells' phenotype, and promising molecular markers and therapeutic targets to support precision medicine in breast and ovarian cancers.
Insights
Non-coding RNAs (ncRNAs), including microRNAs (miRNAs) and long non-coding RNAs (lncRNAs), play crucial roles in breast and ovarian cancers. These powerful gene regulators offer potential as biomarkers and therapeutic targets for personalized cancer medicine.
Area of Science:
- Oncology
- Molecular Biology
- Genomics
Background:
- Tumor molecular hallmarks and novel markers are critical for personalized breast and ovarian cancer treatment.
- Approximately 80% of the genome is transcribed into non-coding RNAs (ncRNAs), challenging the 'junk DNA' concept.
- MicroRNAs (miRNAs) and long non-coding RNAs (lncRNAs) are key regulators of gene expression at multiple levels.
Purpose of the Study:
- To review the involvement of miRNAs and lncRNAs in the molecular basis of breast and ovarian cancers.
- To highlight the clinical utility of ncRNAs in improving disease management.
- To discuss ncRNAs as potential molecular markers and therapeutic targets for precision medicine.
Main Methods:
- Literature review of existing knowledge on ncRNAs in cancer research.
- Analysis of high-throughput studies on genome transcription and ncRNA function.
- Synthesis of information on miRNA and lncRNA deregulation in breast and ovarian tumors.
Main Results:
- ncRNAs, particularly miRNAs and lncRNAs, are actively implicated in various aspects of cancer cell biology.
- Aberrant expression of miRNAs and lncRNAs is observed in both breast and ovarian tumors.
- These ncRNAs are central mediators of cancer cell phenotype.
Conclusions:
- miRNAs and lncRNAs are significant regulators in breast and ovarian malignancies.
- They hold promise as molecular markers for disease monitoring.
- ncRNAs represent promising therapeutic targets for precision oncology in breast and ovarian cancers.
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