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Studies on anticancer activities of antimicrobial peptides.

Abstract
In spite of great advances in cancer therapy, there is considerable current interest in developing anticancer agents with a new mode of action because of the development of resistance by cancer cells towards current anticancer drugs. A growing number of studies have shown that some of the cationic antimicrobial peptides (AMPs), which are toxic to bacteria but not to normal mammalian cells, exhibit a broad spectrum of cytotoxic activity against cancer cells. Such studies have considerably enhanced the significance of AMPs, both synthetic and from natural sources, which have been of importance both for an increased understanding of the immune system and for their potential as clinical antibiotics. The electrostatic attraction between the negatively charged components of bacterial and cancer cells and the positively charged AMPs is believed to play a major role in the strong binding and selective disruption of bacterial and cancer cell membranes, respectively. However, it is unclear why some host defense peptides are able to kill cancer cells when others do not. In addition, it is not clear whether the molecular mechanism(s) underlying the antibacterial and anticancer activities of AMPs are the same or different. In this article, we review various studies on different AMPs that exhibit cytotoxic activity against cancer cells. The suitability of cancer cell-targeting AMPs as cancer therapeutics is also discussed.
AuthorsDavid W Hoskin, Ayyalusamy Ramamoorthy
JournalBiochimica et biophysica acta (Biochim Biophys Acta) Vol. 1778 Issue 2 Pg. 357-75 (Feb 2008) ISSN: 0006-3002 [Print] Netherlands
PMID18078805 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Anti-Infective Agents
  • Antineoplastic Agents
  • Peptides
Topics
  • Amino Acid Sequence
  • Animals
  • Anti-Infective Agents (chemistry, pharmacology)
  • Antineoplastic Agents (pharmacology)
  • Male
  • Mice
  • Molecular Sequence Data
  • Peptides (chemistry, pharmacology)

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