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p53 expression in Wilms' tumor: a possible role as prognostic factor
A J Beniers1, T Efferth, L Füzesi
1Institute of Applied Biomedical Research, NL-6278 NA Gulpen-Wittem, The Netherlands. abeniers@cuci.nl
International Journal of Oncology
|December 15, 2000
Summary
p53 protein expression is linked to unfavorable histology and poor survival in Wilms tumor (WT). This study found p53 positivity in 7 of 21 WT cases, correlating with anaplasia and worse outcomes.
Area of Science:
- Oncology
- Molecular Pathology
- Cancer Genetics
Background:
- Wilms tumor (WT) is a pediatric kidney cancer.
- The prognostic significance of p53 tumor suppressor gene mutations in WT is not fully understood.
- Previous studies suggest a correlation between p53 mutations and anaplasia in WT.
Purpose of the Study:
- To investigate the role and prognostic significance of p53 expression in Wilms tumor.
- To determine the association between p53 expression, tumor histology, and patient survival.
- To identify specific p53 gene mutations in WT cases with altered p53 expression.
Main Methods:
- Immunohistochemical analysis of p53 expression in formalin-fixed paraffin-embedded tumor tissues from 21 WT patients.
- Categorization of tumor histology based on the presence of anaplasia (unfavorable histology).
- Correlation analysis of p53 expression with tumor stage, anaplasia, and patient survival.
- PCR/SSCP and DNA sequencing to analyze p53 gene mutations in selected cases.
Main Results:
- Seven out of 21 (33%) Wilms tumors showed positive p53 expression.
- p53 positivity was significantly correlated with the presence of anaplasia (unfavorable histology).
- p53 expression was also significantly associated with poorer patient survival.
- A specific base change (CGG --> TGG) in codon 282 of exon 8 of the p53 gene was identified in an immunopositive tumor.
Conclusions:
- p53 expression is a potential prognostic marker for poor outcome in Wilms tumor.
- The presence of p53 is closely associated with unfavorable histology, specifically anaplasia.
- Further research is warranted to fully elucidate the role of p53 in WT pathogenesis and progression.