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MiRNAs-mediated cisplatin resistance in breast cancer
Abstract:
Cisplatin is a widely used chemotherapeutic agent in breast cancer treatments with inevitable rapidly acquired resistance or intrinsically resistance. Enormous evidence points to the bioprocesses of resistant formation consisting of diverse miRNAs direct and indirect actions on relevant encoding genes. In this report, we overview detailed information on the miRNAs effect on cisplatin-induced resistance, including alterations in cell survival, modification of DNA damage response, changes in cellular uptake or efflux of the drug, altered DNA methylation, and perturbations in the miRNA biogenesis pathway. This will provide potential miRNA-targeted strategies for the treatment of breast cancer therapy and requires further clinical application.
Insights
MicroRNAs (miRNAs) play a crucial role in cisplatin resistance in breast cancer by affecting drug response and cell survival. Understanding these miRNA mechanisms can lead to novel targeted therapies for improved breast cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Cisplatin is a key chemotherapy for breast cancer.
- Acquired or intrinsic cisplatin resistance is a major clinical challenge.
- MicroRNAs (miRNAs) are implicated in the development of drug resistance.
Purpose of the Study:
- To review the multifaceted roles of miRNAs in cisplatin resistance in breast cancer.
- To elucidate how miRNAs influence key cellular processes related to drug resistance.
Main Methods:
- Literature review of studies investigating miRNA involvement in cisplatin resistance.
- Analysis of miRNA-mediated effects on cell survival, DNA damage, drug transport, and epigenetic modifications.
Main Results:
- miRNAs modulate breast cancer cell survival and response to cisplatin.
- miRNAs impact DNA damage response pathways.
- miRNAs influence drug uptake/efflux and DNA methylation patterns.
- Alterations in miRNA biogenesis pathways contribute to resistance.
Conclusions:
- miRNAs are critical regulators of cisplatin resistance in breast cancer.
- Targeting specific miRNAs offers potential therapeutic strategies.
- Further clinical investigation is needed to translate these findings into effective treatments.
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