Topoisomerase I-DNA Complex Stability Induced by Camptothecins and Its Role in Drug Activity&#

ISSN: 1875-5992 (Online)
ISSN: 1871-5206 (Print)

Volume 17, 14 Issues, 2017

Download PDF Flyer

Anti-Cancer Agents in Medicinal Chemistry

Formerly: Current Medicinal Chemistry - Anti-Cancer Agents

This journal supports open access

Aims & ScopeAbstracted/Indexed in

Ranking and Category:
  • 27th of 59 in Chemistry, Medicinal

Submit Abstracts Online Submit Manuscripts Online

Michelle Prudhomme
Institut de Chimie de Clermont-Ferrand
Université Clermont Auvergne

View Full Editorial Board

Subscribe Purchase Articles Order Reprints

Current: 2.722
5 - Year: 2.849

Topoisomerase I-DNA Complex Stability Induced by Camptothecins and Its Role in Drug Activity&#

Anti-Cancer Agents in Medicinal Chemistry, 4(4): 327-334.

Author(s): Randy M. Wadkins, David Bearss, Govindarajan Manikumar, Mansukhlal C. Wani, Monroe E. Wall and Daniel D Von Hoff.

Affiliation: University of Mississippi, Dept. of Chemistry and Biochemistry, Coulter Hall, Room 409, University, MS 38677


The mechanism of cytotoxicity of the camptothecin family of antitumor drugs is thought to be the consequence of a collision between moving replication forks and camptothecin-stabilized cleavable DNA-topoisomerase I complexes. One property of camptothecin analogs relevant to their potent antitumor activity is the slow reversal of the cleavable complexes formed with these drugs. The persistence of cleavable complexes with time may be an essential property for increasing the likelihood of a collision between the replication fork and a cleavable complex, giving rise to lethal DNA lesions. In this paper, we examined a number of camptothecin analogs forming cleavable complexes with distinctly different stabilities. Absolute reaction rate analysis was carried out for each derivative. Our results indicate that the stability of the cleavable complex is dominated by the activation entropy (ΔS†) of the reversal process. We measured the relative lipophilicity of the CPT analogs by reverse-phase HPLC, but the ΔS† of complex reversal is not directly related to the lipophilicity of the CPT analog being used. We suggest that solvent ordering around the 7- through 10-position of the CPT ring may be responsible for reversal rates dependence on ΔS†. We demonstrate that the cleavable complex stability conferred by each camptothecin analog is directly correlated with the induction of apoptosis and cytotoxicity to tumor cells.


topoisomerase I, camptothecin, cleavable complex, stability, water solubility, kinetics, entropic control.

Purchase Online Order Reprints Order Eprints Rights and Permissions

Article Details

Volume: 4
Issue Number: 4
First Page: 327
Last Page: 334
Page Count: 8
DOI: 10.2174/1568011043352894
Price: $58

Related Journals

Webmaster Contact: Copyright © 2016 Bentham Science