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Expression of E-cadherin and its relation to the p53 protein status in human breast carcinomas
Authors:I K Bukholm  Jahn M Nesland  Rolf Kåresen  U Jacobsen  Anne-Lise Børresen-Dale
Institution:Department of Genetics, The Norwegian Radium Hospital, Montebello, N-0310 Oslo, Norway Tel./Fax: (47)22-93.4440, NO
Department of Pathology, the Norwegian Radium Hospital, University of Oslo, Oslo, Norway, NO
Department of Surgery, Ullev?l Hospital, Norway, NO
Department of Surgery, Buskerud Central Hospital, Norway, NO
Abstract: In breast carcinomas the TP53 gene is altered in 10–30% of cases. Alteration of the gene may lead to a general genomic instability, detected as deletions and/or amplifications at the gene level, and as altered expression at the mRNA and protein level. We have demonstrated a strong association between down-regulation of E-cadherin protein expression and alterations of the p53 protein, detected as TP53 gene mutation and/or protein accumulation in tumour samples from 210 patients with breast carcinomas (P <0.001). Investigation of allelic imbalance using microsatellite markers located near the E-cadherin locus was also performed. A higher frequency of loss of heterozygosity in the microsatellite marker closest to the E-cadherin locus was observed in samples with down-regulation of E-cadherin protein expression. A higher frequency of down-regulation of the E-cadherin protein expression was found in invasive lobular carcinomas than in invasive ductal carcinomas, although this difference was of borderline significant (P=0.084). Cases in the present series were also immunostained for c-erbB-2 protein overexpression. A significant association between p53 protein accumulation and cerbB-2 protein overexpression was seen (P=0.036). The results of the present study indicate that p53 protein may play a role in regulation of E-cadherin protein expression. Received: 29 May 1997)Accepted: 10 June 1997
Keywords:  Breast carcinomas  p53  TP53 gene  E-cadherin  Immunohistochemistry  Genomic instability
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