AI Article Synopsis

  • Doxorubicin is a common breast cancer drug, but cancer cells can develop resistance through mechanisms like ABC transporter overexpression and changes in cell processes.
  • A comprehensive literature review was conducted to investigate the impact of microRNAs on doxorubicin resistance in breast cancer.
  • MicroRNAs influence resistance by regulating key cellular pathways, suggesting that targeted therapies using these molecules could help combat drug resistance and improve treatment outcomes.

Article Abstract

Objectives: Resistance to chemotherapeutic drugs is a serious challenge for effective therapy of cancers. Doxorubicin is a drug which is typically used for breast cancer treatment. Several mechanisms are involved in resistance to doxorubicin including overexpression of ATP-binding cassette (ABC) transporters, altering apoptosis, autophagy and cell cycle arrest. In this review, we focus on the potential effects of microRNAs on doxorubicin resistance in breast cancer.

Methods: Literature review focusing on the 'microRNAs and doxorubicin drug resistance in breast cancer' was conducted comprehensively. The search was performed in PubMed, Scopus, Google and Google Scholar databases and reference lists of relevant articles were also included.

Key Findings: MicroRNAs play essential role in resistance of breast cancer to doxorubicin by affecting several key cellular pathways, including overexpression of ABC transporters, altering apoptosis, autophagy and cell signaling pathways, cell cycle arrest, epithelial to mesenchymal transition (EMT) and cancer stem cells (CSCs).

Conclusions: Cancer treatment methods are moving from conventional therapies to targeted therapies such as using microRNAs. MiRNAs can act as regulatory molecules to overcome breast cancer doxorubicin resistance by controlling the expression levels of genes involved in different cellular pathways. Thus, exact elucidation of their role in different cellular processes can help overcome the breast cancer development and drug resistance.

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Source
http://dx.doi.org/10.1093/jpp/rgaa031DOI Listing

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