Key result
Quercetin pretreatment protected H9C2 cardiomyocytes from doxorubicin-induced cytotoxicity, reducing the apoptotic rate from 61.4% to 9.5%.
Why the study?
Does quercetin prevent doxorubicin-induced cytotoxicity in H9C2 cardiomyocytes?
Does quercetin prevent doxorubicin-induced cytotoxicity in H9C2 cardiomyocytes?
Quercetin protects cardiomyocytes from doxorubicin-induced toxicity in vitro by inhibiting apoptosis and modulating protein folding and cytoskeleton rearrangement.
Answers are grounded in this paper and cite their sources.
No immediate clinical implications; leaves open translation of in vitro protection to doxorubicin cardiotoxicity in patients.
BACKGROUND: Cancer has continually been the leading cause of death worldwide for decades. Thus, scientists have actively devoted themselves to studying cancer therapeutics. Doxorubicin is an efficient drug used in cancer therapy, but also produces reactive oxygen species (ROS) that induce severe cytotoxicity against heart cells. Quercetin, a plant-derived flavonoid, has been proven to contain potent antioxidant and anti-inflammatory properties. Thus, this in vitro study investigated whether quercetin can decrease doxorubicin-induced cytotoxicity and promote cell repair systems in cardiomyocyte H9C2 cells. RESULTS: Proteomic analysis and a cell biology assay were performed to investigate the quercetin-induced responses. Our data demonstrated that quercetin treatment protects the cardiomyocytes in a doxorubicin-induced heart damage model. Quercetin significantly facilitated cell survival by inhibiting cell apoptosis and maintaining cell morphology by rearranging the cytoskeleton. Additionally, 2D-DIGE combined with MALDI-TOF MS analysis indicated that quercetin might stimulate cardiomyocytes to repair damage after treating doxorubicin by modulating metabolic activation, protein folding and cytoskeleton rearrangement. CONCLUSION: Based on a review of the literature, this study is the first to report detailed protective mechanisms for the action of quercetin against doxorubicin-induced cardiomyocyte toxicity based on in-depth cell biology and proteomic analysis.
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Chen et al. (2013) studied Doxorubicin-induced cytotoxicity. Quercetin vs. Doxorubicin alone was evaluated on Apoptotic rate. Quercetin pretreatment protected H9C2 cardiomyocytes from doxorubicin-induced cytotoxicity, reducing the apoptotic rate from 61.4% to 9.5%.
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