Nishiuchi, Shiori Tokushima University
Yagi, Kenta Tokushima University Tokushima University Educator and Researcher Directory
Saito, Hiroumi Tokushima University
Niimura, Takahiro Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Miyata, Koji Tokushima University
Sakamoto, Yoshika Tokushima University
Fukunaga, Kimiko Tokushima University
Ishida, Shunsuke Tokushima University
Aizawa, Fuka Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Goda, Mitsuhiro Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Chuma, Masayuki Asahikawa Medical University
Izawa-Ishizawa, Yuki Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Nawa, Hideki Shujitsu University
Kanda, Yasunari National Institute of Health Sciences
Thesis or Dissertation
Aim: Doxorubicin, an anthracycline anti-tumour agent, is an essential chemotherapeutic drug; however, the adverse events associated with doxorubicin usage, including cardiotoxicity, prevent patients from continuing treatment. Here, we used databases to explore existing approved drugs with potential preventative effects against doxorubicin-induced cardiac events and examined their efficacy and mechanisms.
Methods: The Gene Expression Omnibus (GEO), Library of Integrated Network-based Cellular Signatures (LINCS), and Food and Drug Administration Adverse Events Reporting System (FAERS) databases were used to extract candidate prophylactic drugs. Mouse models of doxorubicin-induced cardiac events were generated by intraperitoneal administration of 20 mg/kg of doxorubicin on Day 1 and oral administration of prophylactic candidate drugs for 6 consecutive days beginning the day before doxorubicin administration. On Day 6, mouse hearts were extracted and examined for mRNA expression of apoptosis-related genes.
Results: GEO analysis showed that doxorubicin administration upregulated 490 genes and downregulated 862 genes, and LINCS data identified sirolimus, verapamil, minoxidil, prednisolone, guanabenz, and mosapride as drugs capable of counteracting these genetic alterations. Examination of the effects of these drugs on cardiac toxicity using FAERS identified sirolimus and mosapride as new prophylactic drug candidates. In model mice, mosapride and sirolimus suppressed the Bax/Bcl-2 mRNA ratio, which is elevated in doxorubicin-induced cardiotoxicity. These drugs also suppressed the expression of inflammatory cytokines Il1b and Il6 and markers associated with myocardial fibrosis, including Lgal3 and Timp1.
Conclusion: These findings suggest that doxorubicin-induced cardiac events are suppressed by the administration of mosapride and sirolimus.
European Journal of Pharmacology
This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
|DOI (Published Version)|
|URL ( Publisher's Version )|
k3698_abstract.pdf 137 KB
k3698_review.pdf 89.4 KB
k3698_fulltext.pdf 594 KB
|MEXT report number||
Doctor of Medical Science