Epithelial-specific loss of PTEN results in colorectal juvenile polyp formation and invasive cancer

Am J Pathol. 2014 Jan;184(1):86-91. doi: 10.1016/j.ajpath.2013.10.003. Epub 2013 Nov 6.

Abstract

Cowden syndrome (CS) is a rare autosomal dominant cancer-prone disorder caused by germ-line mutation of the phosphatase and tensin homolog mutated on chromosome 10 (PTEN) tumor-suppressor gene. Affected patients commonly develop juvenile polyps, and show an elevated risk of developing colorectal cancers. The etiology of these peculiar polyps remains unclear, although previous work has suggested somatic PTEN alterations in the stroma of juvenile polyps. After a long latency period, we find epithelial-specific PTEN deletion to cause formation of juvenile polyps in the colorectum without stromal PTEN loss. More important, we find that these lesions closely recapitulate all of the characteristic histopathological features of juvenile polyps seen in patients with CS, including stromal alterations and dysplastic transformation to colorectal carcinoma. The stromal alterations we identify after epithelial-specific PTEN loss suggest that PTEN may be involved in altered epithelial-mesenchymal cross talk, which, in turn, predisposes to colorectal neoplasia and polyposis. Our transgenic model is the first to recapitulate colorectal juvenile polyposis in patients with CS. We conclude that stromal PTEN loss is not a prerequisite for the formation of juvenile polyps, and that colorectal juvenile polyps in CS are bona fide neoplastic precursor lesions.

MeSH terms

  • Animals
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / pathology
  • Disease Models, Animal*
  • Hamartoma Syndrome, Multiple / genetics
  • Hamartoma Syndrome, Multiple / pathology
  • Immunohistochemistry
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology
  • Intestinal Polyposis / congenital
  • Intestinal Polyposis / genetics
  • Intestinal Polyposis / pathology
  • Intestinal Polyps / genetics*
  • Intestinal Polyps / pathology
  • Mice
  • Mice, Transgenic
  • Neoplastic Syndromes, Hereditary / genetics
  • Neoplastic Syndromes, Hereditary / pathology
  • PTEN Phosphohydrolase / genetics*
  • Precancerous Conditions / genetics*
  • Precancerous Conditions / pathology
  • Stromal Cells / metabolism
  • Stromal Cells / pathology

Substances

  • PTEN Phosphohydrolase
  • Pten protein, mouse

Supplementary concepts

  • Juvenile polyposis syndrome