Smad2/3 linker phosphorylation is a possible marker of cancer stem cells and correlates with carcinogenesis in a mouse model of colitis-associated colorectal cancer

J Crohns Colitis. 2015 Jul;9(7):565-74. doi: 10.1093/ecco-jcc/jjv073. Epub 2015 Apr 23.

Abstract

Background: Epithelial cells affected by somatic mutations undergo transition from a tumour-suppressive to a carcinogenic Smad pathway during sporadic colorectal carcinogenesis, and the specific linker threonine phosphorylation of Smad2/3 in colon epithelial cells indicates stem-like cells. This study extends previous observations to a model of colitis-associated colorectal cancer.

Methods: After Crl:CD-1 mice received an administration of azoxymethane [AOM], the mice were given dextran sodium sulfate [DSS] for 7 days. AOM/DSS-treated mice [AOM/DSS mice] were killed at 10 or 20 weeks. After macroscopic observations, a histopathological analysis was conducted. Immunohistochemical staining was performed using the avidin-biotin immunoperoxidase method [pSmad3C-Ser, pSmad3L-Ser, c-Myc] and immunofluorescent methods [Ki67, β-catenin, CDK4, cyclin D1, Sox9, pSmad2/3L-Thr].

Results: The colons from AOM/DSS mice were shorter than those from control mice. The number of colon tumours at Week 20 was higher than at Week 10. The inflammation scores for AOM/DSS mice were greater than those for control mice. Immunostaining-positive cells (staining by Ki67, β-catenin [nuclear and cytoplasmic], cyclin D1, and Sox9) were diffusely distributed in colon tumours. The percentage of pSmad3L-Ser-positive cells in colon tumours was higher than in sites of pre-neoplastic colitis, and that in sites of pre-neoplastic colitis was higher than in control mice. pSmad2/3L-Thr-positive cells were sparsely detected around crypt bases in non-neoplastic colon epithelia and at the tops of tumours, and immunohistochemical co-localisation of pSmad2/3L-Thr with Ki67 was not observed. Immunohistochemical co-localisation of pSmad2/3L-Thr with β-catenin and CDK4 was observed.

Conclusions: pSmad3L-Ser signalling is an early event in colitis-associated colorectal cancer, and pSmad2/3L-Thr immunostaining-positive cells might be cancer stem cells.

Keywords: Mouse model; Smad; cancer stem cell; carcinogenesis; colitis-associated colorectal cancer; phosphorylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Azoxymethane
  • Biomarkers, Tumor / metabolism
  • Carcinogenesis / metabolism*
  • Carcinogenesis / pathology
  • Colitis / metabolism*
  • Colitis / pathology
  • Colorectal Neoplasms / chemically induced
  • Colorectal Neoplasms / chemistry
  • Colorectal Neoplasms / metabolism*
  • Colorectal Neoplasms / pathology
  • Cyclin D1 / analysis
  • Dextran Sulfate
  • Disease Models, Animal
  • Ki-67 Antigen / analysis
  • Male
  • Mice
  • Neoplastic Stem Cells / metabolism*
  • Phosphorylation
  • Proto-Oncogene Proteins c-myc / analysis
  • SOX9 Transcription Factor / analysis
  • Serine / metabolism
  • Signal Transduction
  • Smad2 Protein / metabolism*
  • Smad3 Protein / analysis
  • Smad3 Protein / metabolism*
  • beta Catenin / analysis

Substances

  • Biomarkers, Tumor
  • Ki-67 Antigen
  • Myc protein, mouse
  • Proto-Oncogene Proteins c-myc
  • SOX9 Transcription Factor
  • Smad2 Protein
  • Smad2 protein, mouse
  • Smad3 Protein
  • Smad3 protein, mouse
  • Sox9 protein, mouse
  • beta Catenin
  • Cyclin D1
  • Serine
  • Dextran Sulfate
  • Azoxymethane