Literature DB >> 7913577

p53 protein and c-erbB-2 protein (p185) expression in endometrial adenocarcinoma of endometrioid type. An immunohistochemical examination on paraffin sections.

A L Nielsen1, H C Nyholm.   

Abstract

The expression of both the nuclear protein p53 tumor suppressor gene product and the transmembrane C-erbB-2 protein oncogene product (p185) correlates to risk factors and outcomes in different tumor types. Their value as prognosticators in endometrial adenocarcinoma of endometrioid type (EC) has not been determined. Paraffin sections were examined immunohistochemically to study the expression of p53 protein and p185 in 112 patients with EC. p53 protein was overaccumulated in 34% and p185 in 13% of the tumors. p53 protein correlated with mitotic count and nuclear grade. Both p53 protein and p185 correlated significantly with outcome. However, they did not correlate with each other or with architectural grade or stage (which defines a high risk group), indicating a role as adjuvant prognosticators in EC. Stage and outcome did correlate, however. Both p53 protein and p185 antibodies work well on routine, formalin-fixed, paraffin-embedded tissue and are easily used in routine diagnostic procedures.

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Year:  1994        PMID: 7913577     DOI: 10.1093/ajcp/102.1.76

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  3 in total

1.  Comparison of benign and malignant endometrial lesions for their p53 state, using immunohistochemistry and temperature-gradient gel electrophoresis.

Authors:  L Riethdorf; C Begemann; S Riethdorf; K Milde-Langosch; T Löning
Journal:  Virchows Arch       Date:  1996-04       Impact factor: 4.064

Review 2.  The clinical significance of p53 aberrations in human tumours.

Authors:  S Bosari; G Viale
Journal:  Virchows Arch       Date:  1995       Impact factor: 4.064

3.  Overexpression of p53 protein is an independent prognostic indicator in human endometrial carcinoma.

Authors:  R Soong; S Knowles; K E Williams; I G Hammond; S J Wysocki; B J Iacopetta
Journal:  Br J Cancer       Date:  1996-08       Impact factor: 7.640

  3 in total

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