Effect of ulinastatin on the expression and distribution of high mobility group box 1 in human colon carcinoma cells in vitro

Mol Med Rep. 2015 Mar;11(3):2041-7. doi: 10.3892/mmr.2014.2921. Epub 2014 Nov 11.

Abstract

The aim of the present study was to investigate the in vitro effects of ulinastatin (UTI) on the proliferation, invasion, apoptosis, expression and distribution of high mobility group box 1 (HMGB1) and the expression of nuclear factor κB (NF‑κB) in human colon carcinoma LoVo cells. The cells were divided into control (untreated), UTI1 (400 U/ml UTI), UTI2 (800 U/ml UTI) and UTI3 (1,600 U/ml UTI) groups. The cell proliferation, invasion, apoptosis and the gene and protein expression of HMGB1 and NF‑κB were detected using a tetrazolium assay, Transwell cell invasion assays, a caspase‑3 activity assay, western blot analysis and reverse transcription quantitative polymerase chain reaction, respectively. The distribution of HMGB1 was detected using immunofluorescence. LoVo cell proilferation decreased the most in the UTI3 group followed, in order, by the UTI2, UTI1 and control groups. UTI inhibited invasion in LoVo cells and the inhibitory effect was enhanced as the UTI concentration increased. The activity of caspase‑3 increased the least in the control group followed, in order, by the UTI1, UTI2 and UTI3 groups. UTI inhibited the expression of HMGB1 and NF‑κB, and decreased the cytoplasmic distribution of HMGB1. Thus, UTI inhibited LoVo cell proliferation and induced LoVo cell apoptosis, the mechanism of which may be associated with a decreased in the expression of HMGB1 and NF‑κB, and the cytoplasmic distribution of HMGB1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma / genetics*
  • Carcinoma / metabolism
  • Caspase 3 / metabolism
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Colonic Neoplasms / genetics*
  • Colonic Neoplasms / metabolism
  • Gene Expression Regulation, Neoplastic / drug effects
  • Glycoproteins / pharmacology*
  • HMGB1 Protein / genetics*
  • Humans
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Trypsin Inhibitors / pharmacology*

Substances

  • Glycoproteins
  • HMGB1 Protein
  • NF-kappa B
  • Trypsin Inhibitors
  • Caspase 3
  • urinastatin