Key result
Curcumin alleviates doxorubicin cardiotoxicity via antioxidant and anti-inflammatory pathways in preclinical models.
Why the study?
The study was designed to review the potential chemoprotective effects of curcumin against doxorubicin-induced cardiotoxicity.
Does curcumin prevent doxorubicin-induced cardiotoxicity in preclinical models?
Systematic Review (n=18)
Does curcumin prevent doxorubicin-induced cardiotoxicity in preclinical models?
Curcumin coadministration demonstrates potential cardioprotective effects against doxorubicin-induced cardiotoxicity in preclinical models through antioxidant, antiapoptotic, and anti-inflammatory mechanisms.
May support adjunctive curcumin with doxorubicin; leaves clinical translation open pending human trials.
OBJECTIVE: This study aimed to review the potential chemoprotective effects of curcumin against the doxorubicin-induced cardiotoxicity. METHODS: According to the PRISMA guideline, a comprehensive systematic search was performed in different electronic databases (Web of Science, PubMed, and Scopus) up to July 2021. One hundred and sixty-four studies were screened in accordance with a predefined set of inclusion and exclusion criteria. Eighteen eligible articles were finally included in the current systematic review. RESULTS: According to the in vitro and in vivo findings, it was found that doxorubicin administration leads to decreased cell survival, increased mortality, decreased bodyweight, heart weight, and heart to the bodyweight ratio compared to the control groups. However, curcumin cotreatment demonstrated an opposite pattern in comparison with the doxorubicin-treated groups alone. Other findings showed that doxorubicin significantly induces biochemical changes in the cardiac cells/tissue. Furthermore, the histological changes on the cardiac tissue were observed following doxorubicin treatment. Nevertheless, for most of the cases, these biochemical and histological changes mediated by doxorubicin were reversed near to control groups following curcumin coadministration. CONCLUSION: It can be mentioned that coadministration of curcumin alleviates the doxorubicin-induced cardiotoxicity. Curcumin exerts these cardioprotective effects through different mechanisms of antioxidant, antiapoptosis, and anti-inflammatory. Since the finding presented in this systematic review are based on in vitro and in vivo studies, suggesting the use of curcumin in cancer patients as a cardioprotector agent against cardiotoxicity mediated by doxorubicin requires further clinical studies.
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Zhang et al. (2022) conducted a systematic review in Doxorubicin-induced cardiotoxicity (n=18). Curcumin vs. Doxorubicin alone was evaluated on Cardiotoxicity (cell survival, mortality, biochemical and histological changes). Coadministration of curcumin alleviates doxorubicin-induced cardiotoxicity through antioxidant, antiapoptotic, and anti-inflammatory mechanisms in in vitro and in vivo models.
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