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<title>European Journal of Pharmaceutical Sciences 1 September 2024</title>
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<dateIssued>2024</dateIssued>
<issuance>monographic</issuance>
<edition>1 September 2024</edition>
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<languageTerm type="text">Indonesia</languageTerm>
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<note>ABSTRACT
Doxorubicin (DOX) is an anthracycline chemotherapy drug widely employed in the treatment of various cancers,
known for its potent antineoplastic properties but often associated with dose-dependent cardiotoxicity, limiting

its clinical use. This review explores the complex molecular details that determine the heart-protective effec-
tiveness of carvedilol in relation to cardiotoxicity caused by DOX. The harmful effects of DOX on heart cells could

include oxidative stress, DNA damage, iron imbalance, disruption of autophagy, calcium imbalance, apoptosis,
dysregulation of topoisomerase 2-beta, arrhythmogenicity, and inflammatory responses. This review carefully
reveals how carvedilol serves as a strong protective mechanism, strategically reducing each aspect of cardiac
damage caused by DOX. Carvedilol&rsquo;s antioxidant capabilities involve neutralizing free radicals and adjusting
crucial antioxidant enzymes. It skillfully manages iron balance, controls autophagy, and restores the calcium
balance essential for cellular stability. Moreover, the anti-apoptotic effects of carvedilol are outlined through the
adjustment of Bcl-2 family proteins and activation of the Akt signaling pathway. The medication also controls

topoisomerase 2-beta and reduces the renin-angiotensin-aldosterone system, together offering a thorough de-
fense against cardiotoxicity induced by DOX. These findings not only provide detailed understanding into the</note>
<subject authority=""><topic>Inflammation</topic></subject>
<subject authority=""><topic>Cardiotoxicity</topic></subject>
<subject authority=""><topic>Doxorubicin</topic></subject>
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<physicalLocation>PERPUSTAKAAN SEKOLAH TINGGI ILMU KESEHATAN SAMARINDA REPOSITORY</physicalLocation>
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<sublocation>Perpus.Akfarsam (Jurnal Farmasi Internasional)</sublocation>
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