NAC1/HMGB1 Signaling Pathway Is Associated with Epithelial-mesenchymal Transition, Invasion, and Metastasis of Lung Cancer Cell Line

Ann Clin Lab Sci. 2018 Sep;48(5):559-564.

Abstract

Objective: This study aims to investigate the role of NAC1/HMGB1 signaling pathway in the epithelial-mesenchymal transition (EMT), invasion, and metastasis of lung cancer cell line.

Methods: Human lung cancer cell line A549 was used in this study. They were randomly divided into normal control group, sh-NAC1 empty vector group (sh-NAC1 NC), expression empty vector group (NAC1 NC), NAC1-shRNA and NAC1 over-expression group (NAC1). NAC1 and HMGB1 expression levels were detected by qRT-PCR method. Cell proliferation was detected by CCK8 kit. Cell cycles were detected by flow cytometry method. Cell invasion was detected by Transwell method. The expression levels of E-cadherin, N-cadherin, NAC1, and HMGB1 were detected by qRT-PCR and Western blotting methods.

Results: Compared with the control group, the expression level of NAC1 and cell proliferation in NAC1-shRNA group decreased, cells in G1 phase increased and cells in S phase decreased. In NAC1-shRNA group, E-cadherin expression levels increased and the expression levels of N-cadherin, HMGB1 and Vimentin decreased. In NAC1 group, the expression level of NAC1 and cell proliferation increased, cells in S phase increased and cells in G1 phase decreased, E-cadherin expression levels decreased and the expression levels of N-cadherin, HMGB1 and Vimentin increased. All these differences are statistically significant.

Conclusions: The expression of NAC1 and HMGB1 in lung cancer cells may affect the occurrence of EMT, the NAC1/ HMGB1 signaling pathway is associated with the EMT, invasion, and metastasis of lung cancer cells.

Keywords: A549; E-cadherin; EMT; HMGB1 signaling pathway; N-cadherin; NAC1.

MeSH terms

  • Antigens, CD / analysis
  • Cadherins / analysis
  • Cell Cycle
  • Cell Line, Tumor
  • Cell Proliferation
  • Epithelial-Mesenchymal Transition*
  • HMGB1 Protein / physiology*
  • Humans
  • Lung Neoplasms / pathology*
  • Neoplasm Invasiveness
  • Neoplasm Metastasis
  • Neoplasm Proteins / analysis
  • Neoplasm Proteins / physiology*
  • Repressor Proteins / analysis
  • Repressor Proteins / physiology*
  • Signal Transduction / physiology*
  • Vimentin / analysis

Substances

  • Antigens, CD
  • CDH1 protein, human
  • Cadherins
  • HMGB1 Protein
  • HMGB1 protein, human
  • NACC1 protein, human
  • Neoplasm Proteins
  • Repressor Proteins
  • VIM protein, human
  • Vimentin