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Regulation of autophagy by microRNAs in human breast cancer
Zhi Xiong Chong1, Swee Keong Yeap2, Wan Yong Ho3
1Faculty of Science and Engineering, University of Nottingham Malaysia, 43500, Semenyih, Selangor, Malaysia.
Abstract:
Breast cancer is the most common solid cancer that affects female population globally. MicroRNAs (miRNAs) are short non-coding RNAs that can regulate post-transcriptional modification of multiple downstream genes. Autophagy is a conserved cellular catabolic activity that aims to provide nutrients and degrade un-usable macromolecules in mammalian cells. A number of in vitro, in vivo and clinical studies have reported that some miRNAs could modulate autophagy activity in human breast cancer cells, and these would influence human breast cancer progression and treatment response. Therefore, this review was aimed to discuss the roles of autophagy-regulating miRNAs in influencing breast cancer development and treatment response. The review would first introduce autophagy types and process, followed by the discussion of the roles of different miRNAs in modulating autophagy in human breast cancer, and to explore how would this miRNA-autophagy regulatory process affect the disease progression or treatment response. Lastly, the potential applications and challenges of utilizing autophagy-regulating miRNAs as breast cancer biomarkers and novel therapeutic agents would be discussed.
Insights
MicroRNAs (miRNAs) regulate autophagy, a cellular process, impacting breast cancer progression and treatment. This review explores how autophagy-modulating miRNAs influence breast cancer development and therapeutic strategies.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Breast cancer is a leading global cancer in women.
- MicroRNAs (miRNAs) are key regulators of gene expression.
- Autophagy is a cellular degradation process crucial for cell homeostasis.
Purpose of the Study:
- To review the role of autophagy-regulating miRNAs in breast cancer.
- To discuss the impact of miRNA-modulated autophagy on breast cancer progression.
- To explore therapeutic and biomarker potential of these miRNAs.
Main Methods:
- Literature review of in vitro, in vivo, and clinical studies.
- Analysis of miRNA roles in modulating autophagy in breast cancer cells.
- Synthesis of findings on disease progression and treatment response.
Main Results:
- Specific miRNAs significantly modulate autophagy in breast cancer.
- Altered autophagy by miRNAs affects tumor development and therapy outcomes.
- miRNA-autophagy interactions present potential therapeutic targets.
Conclusions:
- Autophagy-regulating miRNAs are critical players in breast cancer.
- Targeting miRNA-autophagy pathways may offer novel treatment strategies.
- Further research is needed to harness miRNAs as biomarkers and therapeutics.
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