Home LiteratureArticle Details
PMID: 10692563 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Triapine (3-aminopyridine-2-carboxaldehyde- thiosemicarbazone): A potent inhibitor of ribonucleotide reductase activity with broad spectrum antitumor activity.

Biochemical pharmacology ·Vol. 59 ·No. 8 ·2000-04-15 ·Pages 983-91

Finch RA, Liu M, Grill SP, Rose WC, Loomis R, Vasquez KM, Cheng Y, Sartorelli AC

Abstract

Previous studies from our laboratories have shown that (a) Triapine() is a potent inhibitor of ribonucleotide reductase activity and (b) hydroxyurea-resistant L1210 leukemia cells are fully sensitive to Triapine. In an analogous manner, Triapine was similarly active against the wild-type and a hydroxyurea-resistant subline of the human KB nasopharyngeal carcinoma. Triapine was active in vivo against the L1210 leukemia over a broad range of dosages and was curative for some mice. This agent also caused pronounced inhibition of the growth of the murine M109 lung carcinoma and human A2780 ovarian carcinoma xenografts in mice. Optimum anticancer activity required twice daily dosing due to the duration of inhibition of DNA synthesis which lasted about 10 hr in L1210 cells treated with Triapine in vivo. DNA synthesis in normal mouse tissues (i.e. duodenum and bone marrow) uniformly recovered faster than that in L1210 leukemia cells, demonstrating a pharmacological basis for the therapeutic index of this agent. Triapine was more potent than hydroxyurea in inhibiting DNA synthesis in L1210 cells in vivo, and the effects of Triapine were more pronounced. In addition, the duration of the inhibition of DNA synthesis in leukemia cells from mice treated with Triapine was considerably longer than in those from animals treated with hydroxyurea. Combination of Triapine with various classes of agents that damage DNA (e.g. etoposide, cisplatin, doxorubicin, and 1-acetyl-1,2-bis(methylsulfonyl)-2-(2-chloroethyl)hydrazine) resulted in synergistic inhibition of the L1210 leukemia, producing long-term survivors of tumor-bearing mice treated with several dosage levels of the combinations, whereas no enhancement of survival was found when Triapine was combined with gemcitabine or cytosine arabinoside. The findings demonstrate the superiority of Triapine over hydroxyurea as an anticancer agent and further suggest that prevention by Triapine of repair of DNA lesions created by agents that damage DNA may result in efficacious drug combinations for the treatment of cancer.

MeSH Terms
Animals Antineoplastic Agents/pharmacokinetics,pharmacology,therapeutic use Antineoplastic Combined Chemotherapy Protocols/therapeutic use Blood-Brain Barrier Cell Division/drug effects DNA/biosynthesis,drug effects Drug Resistance, Neoplasm Enzyme Inhibitors/pharmacokinetics,pharmacology,therapeutic use Humans Hydroxyurea/pharmacology KB Cells Leukemia L1210/drug therapy Mice Neoplasm Transplantation Neoplasms, Experimental/drug therapy Pyridines/pharmacokinetics,pharmacology,therapeutic use Ribonucleotide Reductases/antagonists & inhibitors Thiosemicarbazones/pharmacokinetics,pharmacology,therapeutic use Tumor Cells, Cultured
Chemicals
Antineoplastic Agents Enzyme Inhibitors Pyridines Thiosemicarbazones 3-aminopyridine-2-carboxaldehyde thiosemicarbazone DNA Ribonucleotide Reductases Hydroxyurea
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Finch R A
Department of Pharmacology, Cancer Center, Yale University School of Medicine, New Haven, CT, USA.
Liu M
Grill S P
Rose W C
Loomis R
Vasquez K M
Cheng Y
Sartorelli A C
Article Info
Journal
Biochemical pharmacology
Abbr.
Biochem Pharmacol
ISSN
0006-2952
Published
2000-04-15
Pages
983-91
Language
English
Region
England
NLM ID
0101032
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]