Chemotherapy and signaling: How can targeted therapies supercharge cytotoxic agents?

Cancer Biol Ther. 2010 Nov 1;10(9):839-53. doi: 10.4161/cbt.10.9.13738. Epub 2010 Nov 1.

Abstract

In recent years, oncologists have begun to conclude that chemotherapy has reached a plateau of efficacy as a primary treatment modality, even if toxicity can be effectively controlled. Emerging specific inhibitors of signaling and metabolic pathways (i.e., targeted agents) contrast with traditional chemotherapy drugs in that the latter primarily interfere with the DNA biosynthesis and the cell replication machinery. In an attempt to improve on the efficacy, combination of targeted drugs with conventional chemotherapeutics has become a routine way of testing multiple new agents in early phase clinical trials. This review discusses the recent advances including integrative systematic biology and RNAi approaches to counteract the chemotherapy resistance and to buttress the selectivity, efficacy and personalization of anti-cancer drug therapy.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Cell Death
  • Chemotherapy, Adjuvant
  • Drug Resistance, Neoplasm
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Microtubules / drug effects
  • Molecular Targeted Therapy*
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism
  • Protein Kinases / metabolism
  • RNA Interference
  • Signal Transduction / drug effects*

Substances

  • Antineoplastic Agents
  • Intracellular Signaling Peptides and Proteins
  • Protein Kinases