P53 and beta-catenin in colorectal cancer progression

Research output: Contribution to journalArticle

Abstract

Recently a possible cross talk about the relationship between p53 and beta-catenin has been suggested by the observation that colorectal cancers accumulating beta-catenin (as a result of APC mutations) also exhibit high frequency p53 mutations. Our aim was to evaluate the pattern of both the proteins and match these with the morphological changes in colorectal carcinogenesis. Immunohistochemical patterns of p53 and beta catenin were studied using the natural carcinogenetic model of malignant colorectal sporadic adenoma in 27 formalin-fixed paraffin-embedded polyps. We found a progressive increase of p53 and beta-catenin staining from normal, to dysplastic, and to cancerous epithelium. We noted, in dysplastic and cancerous epithelium, but not in normal tissue, the translocation of beta-catenin from the cytoplasm to the nucleus, and in dysplastic epithelium, a significant correlation between p53 over expression and beta-catenin patterns. Beta-catenin cytoplasmic accumulation seemed to drive p53 over expression already in the early stages of carcinogenesis, while nuclear beta-catenin translocation appeared to be related to a pattern of invasion of neoplastic cell.

Original languageEnglish
Pages (from-to)1932-1936
Number of pages5
JournalCurrent Pharmaceutical Design
Volume9
Issue number24
DOIs
Publication statusPublished - 2003

Fingerprint

beta Catenin
Colorectal Neoplasms
Epithelium
Carcinogenesis
Mutation Rate
Polyps
Adenoma
Paraffin
Formaldehyde
Cytoplasm
Staining and Labeling
Mutation

Keywords

  • Beta-catenin
  • Colorectal adenoma
  • Immunohistochemistry
  • p53

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology, Toxicology and Pharmaceutics(all)

Cite this

P53 and beta-catenin in colorectal cancer progression. / Valentini, Anna Maria; Pirrelli, Michele; Renna, Letizia; Armentano, Raffaele; Caruso, Maria Lucia.

In: Current Pharmaceutical Design, Vol. 9, No. 24, 2003, p. 1932-1936.

Research output: Contribution to journalArticle

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