The role of insulin-like growth factor 1 and its receptor in the formation and development of colorectal carcinoma

J Int Med Res. 2013 Aug;41(4):1228-35. doi: 10.1177/0300060513487631. Epub 2013 Jun 25.

Abstract

Objective: To investigate the role of insulin-like growth factor (IGF)-1 and its receptor (IGF1R) in the formation and development of colorectal carcinoma.

Methods: Colorectal tissue and matching serum samples were collected from patients with adenomatous polyps or carcinoma and healthy control subjects. IGF1R mRNA levels were determined via quantitative real-time reverse transcription-polymerase chain reaction. Serum IGF1 was quantified using enzyme-linked immunosorbent assay.

Results: Serum IGF1 concentrations and mucosal IGF1R mRNA levels were significantly higher in patients with adenomatous polyps (n = 24) or carcinoma (n = 13) compared with healthy control subjects (n = 13). There was a significant positive correlation between serum IGF1 and mucosal IGF1R mRNA in patients with adenomatous polyps.

Conclusions: High circulating IGF1 concentrations and mucosal IGF1R expression may play important roles in both the formation and development of colorectal carcinoma. IGF1 and its receptor may be activated before carcinogenesis, and may promote the growth and malignant transformation of adenomatous polyps. IGF1 and IGF1R may be useful biomarkers for evaluating the stage and risk of carcinogenesis.

Keywords: Insulin-like growth factor 1; colorectal carcinoma; colorectal polyps; enzyme-linked immunosorbent assay; insulin-like growth factor receptor; quantitative real-time RT–PCR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / diagnosis
  • Adenocarcinoma / genetics*
  • Adenocarcinoma / metabolism
  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / genetics*
  • Biomarkers, Tumor / metabolism
  • Carcinogenesis / genetics*
  • Carcinogenesis / metabolism
  • Case-Control Studies
  • Colonic Neoplasms / diagnosis
  • Colonic Neoplasms / genetics*
  • Colonic Neoplasms / metabolism
  • Disease Progression
  • Female
  • Gene Expression
  • Humans
  • Insulin-Like Growth Factor I / genetics*
  • Insulin-Like Growth Factor I / metabolism
  • Male
  • Middle Aged
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • Receptor, IGF Type 1 / genetics*
  • Receptor, IGF Type 1 / metabolism

Substances

  • Biomarkers, Tumor
  • RNA, Messenger
  • Insulin-Like Growth Factor I
  • Receptor, IGF Type 1