Anthracyclines and ellipticines as DNA-damaging anticancer drugs: recent advances
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
21839775
DOI
10.1016/j.pharmthera.2011.07.006
PII: S0163-7258(11)00164-1
Knihovny.cz E-resources
- MeSH
- DNA Adducts MeSH
- Anthracyclines pharmacology therapeutic use MeSH
- Ellipticines pharmacology therapeutic use MeSH
- Humans MeSH
- Neoplasms drug therapy metabolism MeSH
- Nanoparticles therapeutic use MeSH
- Drug Carriers therapeutic use MeSH
- DNA Damage * MeSH
- Antineoplastic Agents pharmacology therapeutic use MeSH
- Reactive Oxygen Species metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- DNA Adducts MeSH
- Anthracyclines MeSH
- Ellipticines MeSH
- Drug Carriers MeSH
- Antineoplastic Agents MeSH
- Reactive Oxygen Species MeSH
Over the past forty years, anthracyclines and ellipticines have attracted attention as promising cytostatics. In this review, we focus on their mechanisms of cytoxicity, DNA-damaging effects and adverse side-effects. We also summarize ways to enhance the therapeutic effects of these drugs together with a decrease in their adverse effects. Current drug design strategies are focused on drug bioavailability and their tissue targeting, whereas drug delivery to specific intracellular compartments is rarely addressed. Therefore, therapies utilizing the antineoplastic activities of anthracyclines and ellipticines combined with novel strategies such as nanotechnologies for safer drug delivery, as well as strategies based on gene therapy, could significantly contribute to medical practice.
References provided by Crossref.org
Formation of DNA adducts by ellipticine and its micellar form in rats - a comparative study
A novel insight into the cardiotoxicity of antineoplastic drug doxorubicin