The roles of selenium, insulin-like growth factor binding protein 2 and suppressor of cytokine signaling 3 in the pathogenesis of Kashin-Beck disease

Biomarkers. 2016 Jul;21(5):409-15. doi: 10.3109/1354750X.2016.1141990. Epub 2016 Apr 21.

Abstract

We aimed to verify the levels of IGFBP2 and SOCS3 in cartilage and chondrocytes of Kashin-Beck disease (KBD) patients and the effects of different selenium concentrations on the protein expression levels. Chondrocytes were cultured with sodium selenite in vitro. Immunohistochemistry and western blotting were used to verify the protein expressions. IGFBP2 and SOCS3 were up-regulated in KBD chondrocytes and decreased with increasing selenium concentrations. IGFBP2 expressed highest in the middle zone of KBD cartilage, SOCS3 expressed higher in the middle and deep zone. IGFBP2 and SOCS3 may be the biomarkers for KBD diagnosis and evaluating the effect of selenium supplement.

Keywords: Biomarker; IGF-1 signaling pathway; IGFBP2; SOCS3; chondrocyte; osteoarthropathy.

MeSH terms

  • Biomarkers, Pharmacological / analysis
  • Cartilage, Articular / metabolism
  • Cartilage, Articular / pathology
  • Cells, Cultured
  • Chondrocytes / metabolism
  • Chondrocytes / pathology
  • Gene Expression Regulation / drug effects
  • Humans
  • Insulin-Like Growth Factor Binding Protein 2 / analysis
  • Insulin-Like Growth Factor Binding Protein 2 / physiology*
  • Kashin-Beck Disease / drug therapy
  • Kashin-Beck Disease / etiology
  • Kashin-Beck Disease / pathology*
  • Selenium / pharmacology*
  • Selenium / therapeutic use
  • Suppressor of Cytokine Signaling 3 Protein / analysis
  • Suppressor of Cytokine Signaling 3 Protein / physiology*

Substances

  • Biomarkers, Pharmacological
  • Insulin-Like Growth Factor Binding Protein 2
  • Suppressor of Cytokine Signaling 3 Protein
  • Selenium