Noncoding RNAs in doxorubicin-induced cardiotoxicity and their potential as biomarkers and therapeutic targets

Hong-Ge Fa1,2, Wen-Guang Chang2, Xue-Juan Zhang3

  • 1School of Basic Medical Sciences, Qingdao University, Qingdao, 266021, China.

Insights

Doxorubicin (DOX) cancer treatment causes cardiotoxicity. Noncoding RNAs (ncRNAs) are increasingly studied for their role in DOX cardiotoxicity, offering potential diagnostic and therapeutic strategies.

Area of Science:

  • Cardiovascular Biology
  • Cancer Therapeutics
  • Molecular Biology

Background:

  • Anthracyclines like doxorubicin (DOX) are effective cancer drugs but cause cardiotoxicity, limiting their use.
  • DOX-induced cardiotoxicity significantly impacts cancer survivor health, necessitating better understanding and management.
  • The precise molecular mechanisms underlying DOX cardiotoxicity remain incompletely understood.

Purpose of the Study:

  • To review current research on noncoding RNAs (ncRNAs) in DOX-induced cardiotoxicity.
  • To explore the potential of ncRNAs as diagnostic biomarkers and therapeutic targets for DOX cardiotoxicity.
  • To discuss discrepancies and limitations in the current understanding and application of ncRNAs in this context.

Main Methods:

  • Literature review of studies on ncRNAs (miRNAs, lncRNAs, circRNAs) and DOX cardiotoxicity.
  • Analysis of molecular events and regulatory roles of ncRNAs in cardiovascular system.
  • Synthesis of findings regarding diagnostic and therapeutic prospects.

Main Results:

  • ncRNAs, including microRNAs (miRNAs), long noncoding RNAs (lncRNAs), and circular RNAs (circRNAs), play significant regulatory roles in DOX-induced cardiotoxicity.
  • Emerging evidence highlights the potential of specific ncRNAs as biomarkers for early detection and as therapeutic targets.
  • Research is actively exploring these ncRNAs for clinical applications in managing cardiotoxicity.

Conclusions:

  • ncRNAs represent a promising area for understanding and combating DOX-induced cardiotoxicity.
  • Further research is needed to validate ncRNAs as reliable biomarkers and effective therapeutic agents.
  • Addressing current limitations and discrepancies will be crucial for clinical translation.

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