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Our findings point to a novel cardioprotective role for circulating CgA against doxorubicin-induced cardiotoxicity. Monitoring plasma levels of CgA and/or its fragments before and after chemotherapy in cancer patients might provide important prognostic information regarding drug-related cardiotoxicity. Furthermore, administration of exogenous CgA to patients might represent a novel pharmacological strategy to limit cardiac damage typically associated with anthracycline therapy, particularly in patients with reduced plasma levels of this protein.

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This page is a summary of: Physiological levels of chromogranin A prevent doxorubicin-induced cardiotoxicity without impairing its anticancer activity, The FASEB Journal, April 2019, Federation of American Societies For Experimental Biology (FASEB),
DOI: 10.1096/fj.201802707r.
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