Therapeutic intervention by the simultaneous inhibition of DNA repair and type I or type II DNA topoisomerases: one strategy, many outcomes
Abstract
Many anticancer drugs reduce the integrity of DNA, forming strand breaks. This can cause mutations and cancer or cell death if the lesions are not repaired. Interestingly, DNA repair-deficient cancer cells (e.g., those with BRCA1/2 mutations) have been shown to exhibit increased sensitivity to chemotherapy. Based on this observation, a new therapeutic approach termed 'synthetic lethality' has been developed, in which radiation therapy or cytotoxic anticancer agents are employed in conjunction with selective inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1). Such combinations can cause severe genomic instability in transformed cells resulting in cell death. The synergistic effects of combining PARP-1 inhibition with anticancer drugs have been demonstrated. However, the outcome of this therapeutic strategy varies significantly between cancer types, suggesting that synthetic lethality may be influenced by additional cellular factors. This review focuses on the outcomes of the combined action of PARP-1 inhibitors and agents that affect the activity of DNA topoisomerases.
Citations
-
1 4
CrossRef
-
0
Web of Science
-
1 7
Scopus
Authors (2)
Cite as
Full text
full text is not available in portal
Keywords
Details
- Category:
- Articles
- Type:
- artykuł w czasopiśmie wyróżnionym w JCR
- Published in:
-
Future Medicinal Chemistry
no. 4,
pages 51 - 72,
ISSN: 1756-8919 - Language:
- English
- Publication year:
- 2012
- Bibliographic description:
- Węsierska-Gądek J., Składanowski A.: Therapeutic intervention by the simultaneous inhibition of DNA repair and type I or type II DNA topoisomerases: one strategy, many outcomes// Future Medicinal Chemistry. -Vol. 4, nr. iss. 1 (2012), s.51-72
- DOI:
- Digital Object Identifier (open in new tab) 10.4155/fmc.11.175
- Verified by:
- Gdańsk University of Technology
seen 110 times
Recommended for you
PARP inhibition potentiates the cytotoxic activity of C-1305, a selective inhibitor of topoisomerase II, in human BRCA1-positive breast cancer cells
- J. Węsierska-Gądek,
- N. Zulehner,
- F. Ferk
- + 3 authors
From DNA damage to G2 arrest: the many roles of topoisomerase II. W: Prog-ress in Cell Cycle Research. Ed. Meijer L., Jezequel A., Roberge M. London: Plenum Publ. Comp. Ltd**2003 vol. 5 chapt. 30 s. 295-300 Od uszkodzeń DNA do bloku w G2: wiele ról dla topoizomerazy II.
- A. E. Escargueil,
- A. K. Larsen,
- A. Składanowski
Catalytic topoisomerase II inhibitors in cancer therapy.
- A. E. Escargueil,
- A. K. Larsen,
- A. Składanowski