Expression of p53 in adrenocortical tumours: clinicopathological correlations

J Pathol. 1997 Feb;181(2):146-52. doi: 10.1002/(SICI)1096-9896(199702)181:2<146::AID-PATH744>3.0.CO;2-7.

Abstract

There are limited data to suggest that abnormalities of p53 expression may be a late event in the development of adrenocortical tumours. This has been investigated further by examining a series of adrenocortical adenomas and carcinomas by immunohistochemistry for p53 expression and a subset for evidence of mutation in exons 5-8 of the p53 gene using polymerase chain reaction/single strand conformational polymorphism (PCR/SSCP). In carcinomas, the findings have been correlated with survival data and with tumour ploidy. Immunopositivity for p53 was seen in 4 of 34 adenomas and 22 of 42 carcinomas. Mobility shifts were identified in 1 of 4 adenomas and 10 of 21 carcinomas. There was no correlation between immunostaining pattern or PCR/SSCP evidence of mutation and either survival or disease-free survival in carcinoma. There was also no correlation between p53 status and tumour ploidy. While these findings support a role for p53 in tumour progression, abnormal p53 expression does not appear to have any significant prognostic effect in carcinoma.

MeSH terms

  • Adrenal Cortex Neoplasms / genetics
  • Adrenal Cortex Neoplasms / metabolism*
  • Adrenal Cortex Neoplasms / surgery
  • Adrenocortical Adenoma / genetics
  • Adrenocortical Adenoma / metabolism*
  • Adrenocortical Adenoma / surgery
  • Adrenocortical Carcinoma / genetics
  • Adrenocortical Carcinoma / metabolism*
  • Adult
  • Biomarkers, Tumor / metabolism*
  • Female
  • Genes, p53
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Mutation
  • Neoplasm Proteins / metabolism
  • Ploidies
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Survival Rate
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • Biomarkers, Tumor
  • Neoplasm Proteins
  • Tumor Suppressor Protein p53