Recent trends in cancer drug resistance reversal strategies using nanoparticles

Expert Opin Drug Deliv. 2012 Mar;9(3):287-301. doi: 10.1517/17425247.2012.665365.

Abstract

Introduction: Resistance to chemotherapy is a major obstacle in the successful amelioration of tumors in many cancer patients. Resistance is either intrinsic or acquired, involving mechanisms such as genetic aberrations, decreased influx and increased efflux of drugs. Strategies for the reversal of resistance involve the alteration of enzymes responsible for drug resistance, the modulation of proteins regulating apoptosis mechanisms and improving the uptake of drugs using nanotechnology. Novel strides in the reversal of drug resistance are emerging, involving the use of nanotechnology, targeting stem cells, etc.

Areas covered: This paper reviews the most recent cancer drug reversal strategies involving nanotechnology for targeting cancer cells and cancer stem cells (CSCs), for enhanced uptake of micro- and macromolecular inhibitors.

Expert opinion: Nanotechnology used in conjunction with existing therapies, such as gene therapy and P-glycoprotein inhibition, has been shown to improve the reversal of drug resistance; the mechanisms involved in this include specific targeting of drugs and nucleotide therapeutics, enhanced cellular uptake of drugs and improved bioavailability of drugs with poor physicochemical characteristics. Important strategies in the reversal of drug resistance include: a multifunctional nanoparticulate system housing a targeting moiety; therapeutics to kill resistant cancer cells and CSCs; cytotoxic drugs and a tumor microenvironment stimuli-responsive element, to release the encapsulated therapeutics.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage
  • Aptamers, Nucleotide / administration & dosage
  • Drug Carriers / administration & dosage*
  • Drug Resistance / drug effects
  • Drug Resistance, Multiple
  • Drug Resistance, Neoplasm / drug effects*
  • Humans
  • MicroRNAs / administration & dosage
  • MicroRNAs / antagonists & inhibitors
  • Molecular Targeted Therapy / instrumentation
  • Molecular Targeted Therapy / methods*
  • Nanoparticles / administration & dosage*
  • Neoplasms / drug therapy*
  • Neoplastic Stem Cells / drug effects
  • RNA, Small Interfering / administration & dosage
  • Tumor Microenvironment

Substances

  • Antineoplastic Agents
  • Aptamers, Nucleotide
  • Drug Carriers
  • MicroRNAs
  • RNA, Small Interfering