Apoptosis Induced by Topoisomerase Inhibitors

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

Volume 17, 14 Issues, 2017

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Anti-Cancer Agents in Medicinal Chemistry

Formerly: Current Medicinal Chemistry - Anti-Cancer Agents

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  • 27th of 59 in Chemistry, Medicinal

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

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Apoptosis Induced by Topoisomerase Inhibitors

Anti-Cancer Agents in Medicinal Chemistry, 3(4): 271-290.

Author(s): Olivier Sordet, Qasim A. Khan, Kurt W. Kohn and Yves Pommier.

Affiliation: Bldg. 37, Rm. 5068, NIH, Bethesda MD 20892-4255, USA.


Topoisomerase inhibitors are among the most efficient inducers of apoptosis. The main pathways leading from topoisomerase-mediated DNA damage to cell death involve activation of caspases in the cytoplasm by proapoptotic molecules released from mitochondria. In some cells, apoptotic response also involves the death receptor Fas (APO-1 / CD95). The engagement of these apoptotic effector pathways is tightly controlled by upstream regulatory pathways that respond to DNA lesions-induced by topoisomerase inhibitors in cells undergoing apoptosis. These include the proapoptotic Chk2, c-Abl and SAPK / JNK pathways, the survival PI(3)kinase-Akt-dependent pathway and the transcription factors p53 and NF-κB. Initiation of cellular responses to DNA lesions-induced by topoisomerase inhibitors is ensured by the protein kinases DNA-PK, ATM and ATR, which bind to DNA breaks. These kinases commonly called “DNA sensors” mediate their effects (DNA repair, cell cycle arrest and / or apoptosis) by phosphorylating a large number of substrates, including several downstream kinases such as c-Abl and the checkpoint protein Chk2. c-Abl induces apoptosis by activating cell death pathways (e.g., SAPK, p53 and p73) and inhibiting cell survival pathways [e.g., PI(3)kinase]. The DNA-damage regulating kinase Chk2, in addition to its role in cell cycle arrest and / or DNA repair, can induce apoptosis by phosphorylation / activation of the promyelocytic leukemia (PML) protein and p53. Finally, we will review the recent observations that support a role for topoisomerases in chromatin fragmentation during the execution phase of apoptosis.


topoisomerase, apoptosis, c-abl, chk2.

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Article Details

Volume: 3
Issue Number: 4
First Page: 271
Last Page: 290
Page Count: 20
DOI: 10.2174/1568011033482378
Price: $58
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