Information Theory: New Look at Oncogenic Signaling Pathways

Trends Cell Biol. 2019 Nov;29(11):862-875. doi: 10.1016/j.tcb.2019.08.005. Epub 2019 Oct 17.

Abstract

Sustained pro-proliferative signaling is one of the hallmarks of cancer. Although it is generally understood that the oncogenic signaling pathways are overactivated, or at least abnormally activated, in cancer cells, important mechanistic details of such abnormal activation remain unresolved. Among these details are such aspects of signaling as robustness, redundancy, signal amplification, and others, which touch upon the domain of information theory - the field of mathematics and engineering dealing with properties of information storage, encoding, and transmission. Information theory only recently has started to be applied to intracellular signaling. Here, we overview the recent advances provided by the information theory, focusing on the nuclear factor (NF)-κB, extracellular signal-regulated kinase (ERK), and G-protein-coupled receptor (GPCR) pathways, which are frequently hijacked in cancer. Furthermore, we show how viewing previously untouched mechanics of oncogenic signaling through information theory applications may evolve into novel ways of anticancer drug discovery.

Keywords: ERK; GPCR; NF-κB; cancer; drug discovery; information theory; signaling.

Publication types

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

MeSH terms

  • Carcinogenesis / pathology*
  • Cell Proliferation
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Humans
  • Information Theory*
  • NF-kappa B / metabolism
  • Neoplasms / pathology*
  • Receptors, G-Protein-Coupled / metabolism
  • Signal Transduction / physiology*

Substances

  • NF-kappa B
  • Receptors, G-Protein-Coupled
  • Extracellular Signal-Regulated MAP Kinases