Evasion of anti-growth signaling: A key step in tumorigenesis and potential target for treatment and prophylaxis by natural compounds

Semin Cancer Biol. 2015 Dec:35 Suppl:S55-S77. doi: 10.1016/j.semcancer.2015.02.005. Epub 2015 Mar 6.

Abstract

The evasion of anti-growth signaling is an important characteristic of cancer cells. In order to continue to proliferate, cancer cells must somehow uncouple themselves from the many signals that exist to slow down cell growth. Here, we define the anti-growth signaling process, and review several important pathways involved in growth signaling: p53, phosphatase and tensin homolog (PTEN), retinoblastoma protein (Rb), Hippo, growth differentiation factor 15 (GDF15), AT-rich interactive domain 1A (ARID1A), Notch, insulin-like growth factor (IGF), and Krüppel-like factor 5 (KLF5) pathways. Aberrations in these processes in cancer cells involve mutations and thus the suppression of genes that prevent growth, as well as mutation and activation of genes involved in driving cell growth. Using these pathways as examples, we prioritize molecular targets that might be leveraged to promote anti-growth signaling in cancer cells. Interestingly, naturally occurring phytochemicals found in human diets (either singly or as mixtures) may promote anti-growth signaling, and do so without the potentially adverse effects associated with synthetic chemicals. We review examples of naturally occurring phytochemicals that may be applied to prevent cancer by antagonizing growth signaling, and propose one phytochemical for each pathway. These are: epigallocatechin-3-gallate (EGCG) for the Rb pathway, luteolin for p53, curcumin for PTEN, porphyrins for Hippo, genistein for GDF15, resveratrol for ARID1A, withaferin A for Notch and diguelin for the IGF1-receptor pathway. The coordination of anti-growth signaling and natural compound studies will provide insight into the future application of these compounds in the clinical setting.

Keywords: Anti-growth signaling; Cancer prevention; Hallmark of cancer; Reversible and irreversible evasion; Tumor suppressor.

Publication types

  • Review

MeSH terms

  • Carcinogenesis / genetics*
  • Cell Proliferation / genetics*
  • DNA-Binding Proteins
  • Growth Differentiation Factor 15 / genetics
  • Hippo Signaling Pathway
  • Humans
  • Kruppel-Like Transcription Factors / genetics
  • Molecular Targeted Therapy
  • Neoplasms / genetics*
  • Neoplasms / therapy*
  • Nuclear Proteins / genetics
  • PTEN Phosphohydrolase / genetics
  • Protein Serine-Threonine Kinases / genetics
  • Retinoblastoma Protein / genetics
  • Signal Transduction*
  • Somatomedins / genetics
  • Transcription Factors / genetics
  • Tumor Suppressor Protein p53 / genetics

Substances

  • ARID1A protein, human
  • DNA-Binding Proteins
  • GDF15 protein, human
  • Growth Differentiation Factor 15
  • KLF5 protein, human
  • Kruppel-Like Transcription Factors
  • Nuclear Proteins
  • Retinoblastoma Protein
  • Somatomedins
  • TP53 protein, human
  • Transcription Factors
  • Tumor Suppressor Protein p53
  • Protein Serine-Threonine Kinases
  • PTEN Phosphohydrolase
  • PTEN protein, human