Drug intelligence / Profile preview

5-fluorouracil + cisplatin + dexrazoxane + doxorubicin + vincristine

Development stage
Unknown
Lead developer
Michigan State University
Modality
Small Molecules
Administration
Intravenous
01

Overview

This is a combination chemotherapy regimen consisting of five agents: 5-fluorouracil, cisplatin, dexrazoxane, doxorubicin, and vincristine. Each component has a distinct mechanism of action targeting cancer cells: - 5-fluorouracil is an antimetabolite that inhibits thymidylate synthase, blocking DNA synthesis. - Cisplatin is a platinum-based compound that forms DNA crosslinks and induces apoptosis. - Dexrazoxane acts as a cardioprotective agent by chelating iron and reducing free radical formation; it is often used to mitigate the cardiotoxicity associated with anthracyclines like doxorubicin. - Doxorubicin is an anthracycline antibiotic that intercalates into DNA and inhibits topoisomerase II, leading to DNA damage. - Vincristine disrupts microtubule formation during mitosis. This multi-agent regimen aims to maximize anti-tumor efficacy by combining drugs with complementary mechanisms. Such regimens are primarily used in pediatric oncology for conditions like hepatoblastoma or other solid tumors where aggressive multi-drug therapy may be indicated[1][2][6]. The addition of dexrazoxane specifically helps reduce the risk of cardiac toxicity from doxorubicin.

02

Targets

TS (Thymidylate synthase)TOP2A (DNA topoisomerase II)DNATUBB (Tubulin (alpha and beta subunits))TOP2B (DNA topoisomerase II beta)

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