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Monitoring of Nanodrug Accumulation in Murine Breast Cancer Metastases
Published on: August 23, 2024
microRNAs targeting cellular cholesterol: implications for combating anticancer drug resistance
Bernice Monchusi1, Mandeep Kaur1
1School of Molecular and Cell Biology, University of Witwatersrand, Wits, Johannesburg, South Africa.
Abstract:
Over sixty percent of all mammalian protein-coding genes are estimated to be regulated by microRNAs (miRNAs), and unsurprisingly miRNA dysregulation has been linked with cancer. Aberrant miRNA expression in cancer cells has been linked with tumourigenesis and drug resistance. In the past decade, increasing number of studies have demonstrated that cholesterol accumulation fuels tumour growth and contributes to drug resistance, therefore, miRNAs controlling cholesterol metabolism and homeostasis are obvious hypothetical targets for investigating their role in cholesterol-mediated drug resistance in cancer. In this review, we have collated published evidences to consolidate this hypothesis and have scrutinized it by utilizing computational tools to explore the role of miRNAs in cholesterol-mediated drug resistance in breast cancer cells. We found that hsa-miR-128 and hsa-miR-223 regulate genes mediating lipid signalling and cholesterol metabolism, cancer drug resistance and breast cancer genes. The analysis demonstrates that targeting these miRNAs in cancer cells presents an opportunity for developing new strategies to combat anticancer drug resistance.
Insights
MicroRNAs (miRNAs) regulate genes involved in cholesterol metabolism. Targeting specific miRNAs like hsa-miR-128 and hsa-miR-223 may overcome drug resistance in breast cancer.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- Over 60% of mammalian protein-coding genes are regulated by microRNAs (miRNAs).
- miRNA dysregulation is linked to cancer, influencing tumorigenesis and drug resistance.
- Cholesterol accumulation fuels tumor growth and contributes to drug resistance in cancer cells.
Purpose of the Study:
- To investigate the role of miRNAs in cholesterol-mediated drug resistance in breast cancer.
- To consolidate evidence on miRNAs controlling cholesterol metabolism and their link to cancer drug resistance.
- To explore potential therapeutic strategies targeting miRNAs for overcoming drug resistance.
Main Methods:
- Literature review and collation of published evidence.
- Computational tools analysis to explore miRNA roles.
- Focus on breast cancer cells and cholesterol metabolism.
Main Results:
- hsa-miR-128 and hsa-miR-223 were identified as key regulators.
- These miRNAs target genes involved in lipid signaling, cholesterol metabolism, and breast cancer pathways.
- Evidence supports their role in mediating cholesterol-driven drug resistance.
Conclusions:
- miRNAs controlling cholesterol metabolism are implicated in cancer drug resistance.
- Targeting hsa-miR-128 and hsa-miR-223 presents a potential strategy to combat drug resistance in breast cancer.
- Further research into miRNA-based therapies could enhance cancer treatment outcomes.
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