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Long non-coding RNAs in breast cancer metastasis
Priya Mondal1,2, Syed Musthapa Meeran1,2
1Laboratory of Cancer Epigenetics, Department of Biochemistry, CSIR-Central Food Technological Research Institute, Mysore, 570020, India.
Non-Coding RNA Research
|December 9, 2020
Summary
Long non-coding RNAs (lncRNAs) are key epigenetic modifiers regulating breast cancer metastasis. This review details how lncRNAs influence metastasis through miRNA sponging and gene expression, impacting survival rates.
Area of Science:
- Oncology
- Molecular Biology
- Epigenetics
Background:
- Breast cancer is a leading cause of cancer death in women, with metastasis significantly reducing survival rates.
- Metastasis involves complex processes including epithelial-mesenchymal transition (EMT), invasion, and colonization.
- Epigenetic modifications, particularly by long non-coding RNAs (lncRNAs), are implicated in tumor progression and metastasis.
Purpose of the Study:
- To review the critical role of lncRNAs in regulating breast cancer metastasis.
- To elucidate the molecular mechanisms by which lncRNAs influence metastatic processes.
- To identify key lncRNAs involved in breast cancer invasion and metastasis.
Main Methods:
- Literature review focusing on lncRNA functions in cancer metastasis.
- Analysis of studies detailing lncRNA interactions with miRNAs and mRNAs.
- Examination of lncRNA's impact on gene expression and cell signaling pathways.
Main Results:
- lncRNAs act as epigenetic modifiers, significantly impacting breast cancer metastasis.
- Mechanisms include miRNA sponging, mRNA degradation/silencing, and modulation of gene expression.
- Specific lncRNAs regulate genes and pathways crucial for invasion and secondary site colonization.
Conclusions:
- lncRNAs are pivotal regulators of breast cancer metastasis through diverse epigenetic mechanisms.
- Understanding lncRNA functions offers potential therapeutic targets for metastatic breast cancer.
- Further research into lncRNA roles can improve treatment strategies and patient outcomes.
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