Overexpression of ING5 inhibits HGF-induced proliferation, invasion and EMT in thyroid cancer cells via regulation of the c-Met/PI3K/Akt signaling pathway

Biomed Pharmacother. 2018 Feb:98:265-270. doi: 10.1016/j.biopha.2017.12.045. Epub 2017 Dec 27.

Abstract

The inhibitor of growth 5 (ING5), a novel member of the ING family, is involved in diverse biological processes such as cell growth, apoptosis and DNA repair. Recently, ING5 has been reported to be associated with cancer development. However, its specific role in thyroid cancer has yet to be elucidated. In this study, we found that the expression of ING5 was significantly down-regulated in human thyroid cancer tissues and cell lines. In addition, overexpression of ING5 markedly inhibited hepatocyte growth factor (HGF)-induced proliferation, invasion and epithelial-mesenchymal transition (EMT) of thyroid cancer cells as well as suppressed the tumor growth and metastasis in vivo. Furthermore, our data showed that the c-Met/PI3K/Akt signaling pathway was responsible for the inhibitory effect of ING5 on the thyroid cancer. Taken together, these findings provided an essential basis for the tumor-suppression role of ING5 in thyroid cancer.

Keywords: EMT; ING5; Invasion; Proliferation; Thyroid cancer.

MeSH terms

  • Animals
  • Cell Proliferation / drug effects
  • Cell Proliferation / physiology
  • Epithelial-Mesenchymal Transition / drug effects
  • Epithelial-Mesenchymal Transition / physiology*
  • Gene Expression Regulation, Neoplastic
  • Hepatocyte Growth Factor / antagonists & inhibitors
  • Hepatocyte Growth Factor / pharmacology
  • Humans
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neoplasm Invasiveness / pathology
  • Phosphatidylinositol 3-Kinases / physiology*
  • Proto-Oncogene Proteins c-akt / physiology*
  • Proto-Oncogene Proteins c-met / physiology*
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Thyroid Neoplasms / metabolism*
  • Thyroid Neoplasms / pathology
  • Transcription Factors / biosynthesis*
  • Transcription Factors / genetics
  • Tumor Suppressor Proteins / biosynthesis*
  • Tumor Suppressor Proteins / genetics

Substances

  • ING5 protein, human
  • Transcription Factors
  • Tumor Suppressor Proteins
  • Hepatocyte Growth Factor
  • Phosphatidylinositol 3-Kinases
  • MET protein, human
  • Proto-Oncogene Proteins c-met
  • Proto-Oncogene Proteins c-akt