Expressions of IGF-1, ERK, GLUT4, IRS-1 in metabolic syndrome complicated with colorectal cancer and their associations with the clinical characteristics of CRC

Cancer Biomark. 2018;21(4):883-891. doi: 10.3233/CBM-170942.

Abstract

Background: Epidemiological data have revealed that colorectal cancer (CRC) risk is increased in patients with Metabolic syndrome.

Objective: To explore the expressions of IGF-1, ERK, GLUT4, IRS-1 in MS patients with CRC and their associations with the clinical characteristics of CRC.

Methods: We investigated the expressions of IGF-1, ERK, GLUT4 and IRS-1 in greater omental adipose tissues of 168 MS patients with/without CRC, 85 CRC patients without MS and 98 healthy controls by RT-PCR, and analyzed the relationships between their expressions and clinical characteristics of CRC.

Results: The expression levels of IGF-1 and ERK in MS patients with/without CRC were higher while the expression levels of GLUT4 were lower compared with CRC patients without MS and healthy controls (P< 0.01). The expression levels of IGF-1 and ERK in MS patients with CRC were higher while expression levels of GLUT4 were lower compared to MS patients without CRC (P< 0.01). Expression levels of ERK, IGF-1, GLUT4 were associated with clinical characteristics of CRC, including tumor size, distant metastasis and advanced stages (III/IV) (P< 0.05).

Conclusions: Expressions of IGF-1, ERK and GLUT4 in greater omental adipose tissues might be useful biomarkers and predictive targets in the diagnosis of CRC.

Keywords: ERK; GLUT4; IGF-1; Metabolic syndrome; colorectal cancer.

MeSH terms

  • Adipose Tissue / metabolism
  • Adipose Tissue / pathology
  • Adult
  • Aged
  • Biomarkers, Tumor / analysis*
  • Colorectal Neoplasms / complications*
  • Colorectal Neoplasms / pathology
  • Extracellular Signal-Regulated MAP Kinases / analysis
  • Extracellular Signal-Regulated MAP Kinases / biosynthesis
  • Female
  • Glucose Transporter Type 4 / analysis
  • Glucose Transporter Type 4 / biosynthesis
  • Humans
  • Insulin Receptor Substrate Proteins / analysis
  • Insulin Receptor Substrate Proteins / biosynthesis
  • Insulin-Like Growth Factor I / analysis
  • Insulin-Like Growth Factor I / biosynthesis
  • Male
  • Metabolic Syndrome / complications*
  • Middle Aged
  • Omentum / metabolism
  • Omentum / pathology

Substances

  • Biomarkers, Tumor
  • Glucose Transporter Type 4
  • IGF1 protein, human
  • IRS1 protein, human
  • Insulin Receptor Substrate Proteins
  • SLC2A4 protein, human
  • Insulin-Like Growth Factor I
  • Extracellular Signal-Regulated MAP Kinases