Synergistic antitumor activity from two-stage delivery of targeted toxins and endosome-disrupting nanoparticles

Biomacromolecules. 2013 Apr 8;14(4):1093-102. doi: 10.1021/bm3019906. Epub 2013 Mar 11.

Abstract

Plant-derived Type I toxins are candidate anticancer therapeutics requiring cytosolic delivery into tumor cells. We tested a concept for two-stage delivery, whereby tumor cells precoated with an antibody-targeted gelonin toxin were killed by exposure to endosome-disrupting polymer nanoparticles. Co-internalization of particles and tumor cell-bound gelonin led to cytosolic delivery and >50-fold enhancement of toxin efficacy. This approach allows the extreme potency of gelonin to be focused on tumors with significantly reduced potential for off-target toxicity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Antibodies
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents, Phytogenic / administration & dosage*
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Cell Line, Tumor
  • Dextrans / metabolism
  • Drug Carriers*
  • Endosomes / metabolism*
  • Humans
  • Mice
  • Nanoparticles
  • Neoplasms / drug therapy*
  • Phalloidine / administration & dosage*
  • Ribosome Inactivating Proteins, Type 1 / administration & dosage*
  • Ribosome Inactivating Proteins, Type 1 / chemistry
  • Ribosome Inactivating Proteins, Type 1 / pharmacology

Substances

  • Antibodies
  • Antineoplastic Agents
  • Antineoplastic Agents, Phytogenic
  • Dextrans
  • Drug Carriers
  • Ribosome Inactivating Proteins, Type 1
  • Phalloidine
  • GEL protein, Gelonium multiflorum