Therapeutic cancer targeting peptides

Olulanu H. Aina, Thomas C. Sroka, Man Ling Chen, Kit Lam

Research output: Contribution to journalArticle

249 Scopus citations

Abstract

Antitumor monoclonal antibodies have shown clinical promise as cancer cell surface targeting agents. More tumor targeting antibodies are likely to be approved by the FDA in the next few years. However, there are two major limitations in antibody-targeted therapy: large size and nonspecific uptake of the antibody molecules by the liver and the reticuloendothelial system. These result in poor tumor penetration of antibody pharmaceuticals and dose-limiting toxicity to the liver and bone marrow. Peptides are excellent alternative targeting agents for human cancers, and they may alleviate some of the problems with antibody targeting. In the last decade, several investigators have successfully used combinatorial library methods to discover cell surface binding peptides that may be useful for cancer targeting. The phage-display library technique and the "one-bead one-compound" combinatorial library method are the two approaches that have been used. Cancer cell surface receptors or endothelial cell surface receptors of the neovasculature are the two popular therapeutic targets for cancer. Results from preclinical studies with some peptides are encouraging in their targeting potential.

Original languageEnglish (US)
Pages (from-to)184-199
Number of pages16
JournalBiopolymers - Peptide Science Section
Volume66
Issue number3
DOIs
StatePublished - 2002

Keywords

  • Cancer targeting
  • Cancer therapy
  • Chemical microarray
  • Combinatorial chemistry
  • Monoclonal antibody
  • Phage-display peptide library
  • Therapeutic peptide

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Biochemistry
  • Biophysics

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