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Clinicopathological Analysis of miRNA Expression in Breast Cancer Tissues by Using miRNA In Situ Hybridization
Published on: June 7, 2016
MiRNAs and Other Epigenetic Changes as Biomarkers in Triple Negative Breast Cancer
Andrea Mathe1,2, Rodney J Scott3,4,5, Kelly A Avery-Kiejda6,7
1Centre for Information Based Medicine, Hunter Medical Research Institute, Newcastle, NSW 2305, Australia. andrea.mathe@uon.edu.au.
Abstract:
Triple negative breast cancer (TNBC) is characterised by the lack of receptors for estrogen (ER), progesterone (PR), and human epidermal growth factor 2 (HER2). Since it cannot be treated by current endocrine therapies which target these receptors and due to its aggressive nature, it has one of the worst prognoses of all breast cancer subtypes. The only treatments remain chemo- and/or radio-therapy and surgery and because of this, novel biomarkers or treatment targets are urgently required to improve disease outcomes. MicroRNAs represent an attractive candidate for targeted therapies against TNBC, due to their natural ability to act as antisense interactors and regulators of entire gene sets involved in malignancy and their superiority over mRNA profiling to accurately classify disease. Here we review the current knowledge regarding miRNAs as biomarkers in TNBC and their potential use as therapeutic targets in this disease. Further, we review other epigenetic changes and interactions of these changes with microRNAs in this breast cancer subtype, which may lead to the discovery of new treatment targets for TNBC.
Insights
Triple negative breast cancer (TNBC) lacks key receptors, making it hard to treat. MicroRNAs show promise as biomarkers and therapeutic targets for this aggressive cancer.
Area of Science:
- Oncology
- Molecular Biology
- Epigenetics
Background:
- Triple negative breast cancer (TNBC) lacks estrogen, progesterone, and HER2 receptors.
- TNBC has an aggressive nature and poor prognosis, necessitating novel treatment strategies.
- Current treatments for TNBC are limited to chemotherapy, radiotherapy, and surgery.
Purpose of the Study:
- To review current knowledge on microRNAs (miRNAs) as biomarkers for TNBC.
- To explore the potential of miRNAs as therapeutic targets in TNBC.
- To examine epigenetic changes and their interaction with miRNAs in TNBC for new treatment discovery.
Main Methods:
- Literature review of current research on miRNAs and TNBC.
- Analysis of miRNA roles in gene regulation and malignancy.
- Investigation of epigenetic modifications in breast cancer subtypes.
Main Results:
- MicroRNAs are effective regulators of gene sets involved in malignancy.
- miRNAs demonstrate superiority over mRNA profiling for accurate disease classification.
- Epigenetic changes, interacting with miRNAs, offer potential new therapeutic avenues.
Conclusions:
- MicroRNAs are promising biomarkers for TNBC diagnosis and prognosis.
- Targeting miRNAs presents a viable therapeutic strategy for TNBC.
- Further research into miRNA-epigenetic interactions may uncover novel TNBC treatments.
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