Immunology in the clinic review series; focus on cancer: multiple roles for the immune system in oncogene addiction

Clin Exp Immunol. 2012 Feb;167(2):188-94. doi: 10.1111/j.1365-2249.2011.04514.x.

Abstract

Despite complex genomic and epigenetic abnormalities, many cancers are irrevocably dependent on an initiating oncogenic lesion whose restoration to a normal physiological activation can elicit a dramatic and sudden reversal of their neoplastic properties. This phenomenon of the reversal of tumorigenesis has been described as oncogene addiction. Oncogene addiction had been thought to occur largely through tumour cell-autonomous mechanisms such as proliferative arrest, apoptosis, differentiation and cellular senescence. However, the immune system plays an integral role in almost every aspect of tumorigenesis, including tumour initiation, prevention and progression as well as the response to therapeutics. Here we highlight more recent evidence suggesting that oncogene addiction may be integrally dependent upon host immune-mediated mechanisms, including specific immune effectors and cytokines that regulate tumour cell senescence and tumour-associated angiogenesis. Hence, the host immune system is essential to oncogene addiction.

Publication types

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

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • CD4-Positive T-Lymphocytes / immunology
  • Cell Transformation, Neoplastic / immunology
  • Cellular Senescence / genetics
  • Combined Modality Therapy
  • Cytokines / physiology
  • Gene Knockdown Techniques
  • Humans
  • Immunotherapy
  • Mice
  • Mice, Transgenic
  • Molecular Targeted Therapy
  • Neoplasms / genetics
  • Neoplasms / immunology*
  • Neoplasms / pathology
  • Neoplasms / therapy
  • Neovascularization, Pathologic / drug therapy
  • Neovascularization, Pathologic / genetics
  • Neovascularization, Pathologic / immunology
  • Oncogene Proteins / antagonists & inhibitors
  • Oncogene Proteins / physiology*
  • Oncogenes*
  • Tumor Suppressor Proteins / physiology

Substances

  • Antineoplastic Agents
  • Cytokines
  • Oncogene Proteins
  • Tumor Suppressor Proteins