Tumor-related interleukins: old validated targets for new anti-cancer drug development

Mol Cancer. 2017 Sep 19;16(1):153. doi: 10.1186/s12943-017-0721-9.

Abstract

In-depth knowledge of cancer molecular and cellular mechanisms have revealed a strong regulation of cancer development and progression by the inflammation which orchestrates the tumor microenvironment. Immune cells, residents or recruited, in the inflammation milieu can have rather contrasting effects during cancer development. Accumulated clinical and experimental data support the notion that acute inflammation could exert an immunoprotective effect leading to tumor eradication. However, chronic immune response promotes tumor growth and invasion. These reactions are mediated by soluble mediators or cytokines produced by either host immune cells or tumor cells themselves. Herein, we provide an overview of the current understanding of the role of the best-validated cytokines involved in tumor progression, IL-1, IL-4 and IL-6; in addition to IL-2 cytokines family, which is known to promote tumor eradication by immune cells. Furthermore, we summarize the clinical attempts to block or bolster the effect of these tumor-related interleukins in anti-cancer therapy development.

Keywords: Anti-cancer; Cancer; Cytokines; Immune cells; Tumor microenvironment.

Publication types

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

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Biomarkers
  • Drug Discovery
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunomodulation
  • Interleukin-2 / genetics
  • Interleukin-2 / metabolism
  • Interleukin-2 / pharmacology
  • Interleukin-2 / therapeutic use
  • Interleukins / genetics*
  • Interleukins / metabolism*
  • Interleukins / pharmacology
  • Interleukins / therapeutic use
  • Molecular Targeted Therapy
  • Neoplasms / drug therapy
  • Neoplasms / genetics*
  • Neoplasms / metabolism*
  • Neoplasms / pathology
  • Signal Transduction
  • Tumor Microenvironment / drug effects
  • Tumor Microenvironment / genetics
  • Tumor Microenvironment / immunology

Substances

  • Antineoplastic Agents
  • Biomarkers
  • Interleukin-2
  • Interleukins