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p53 protein expression patterns associated with TP53 mutations in breast carcinoma.
Anderson, Sarah A; Bartow, Brooke B; Harada, Shuko; Siegal, Gene P; Wei, Shi; Dal Zotto, Valeria L; Huang, Xiao.
Afiliação
  • Anderson SA; Department of Pathology, The University of Alabama at Birmingham, 619 19th Street South, Birmingham, AL, 35294, USA.
  • Bartow BB; Department of Pathology, The University of Alabama at Birmingham, 619 19th Street South, Birmingham, AL, 35294, USA.
  • Harada S; Department of Pathology, The University of Alabama at Birmingham, 619 19th Street South, Birmingham, AL, 35294, USA.
  • Siegal GP; Department of Pathology, The University of Alabama at Birmingham, 619 19th Street South, Birmingham, AL, 35294, USA.
  • Wei S; Department of Pathology, The University of Alabama at Birmingham, 619 19th Street South, Birmingham, AL, 35294, USA.
  • Dal Zotto VL; Department of Pathology, The University of Alabama at Birmingham, 619 19th Street South, Birmingham, AL, 35294, USA.
  • Huang X; Department of Pathology, The University of Alabama at Birmingham, 619 19th Street South, Birmingham, AL, 35294, USA. xiaohuang@uabmc.edu.
Breast Cancer Res Treat ; 207(1): 213-222, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38900212
ABSTRACT

PURPOSE:

The importance of a TP53 mutation has been demonstrated in several tumor types, including breast cancer (BC). However, the accuracy of p53 protein expression as a predictor of gene mutation has not been well studied in BC. Therefore, we evaluated p53 protein expression associated with TP53 mutations in breast cancers from 64 patients.

METHODS:

TP53 mutation was examined using next-generation sequencing (NGS). p53 protein expression was examined using immunohistochemistry (IHC).

RESULTS:

Among the 64 BCs, 55% demonstrated abnormal expression patterns including 27% overexpression, 22% null, 6% equivocal with 45% having a wild-type pattern. A TP53 mutation was present in 53% (34/64) of tumors including 30% (19/64) demonstrating a missense mutation, 11% (7/64) with a frameshift mutation, 11% (7/64) with a nonsense mutation, and 3% (1/64) with a splice site mutation. Abnormal expression of p53 protein was present in 33 of 34 (97%) tumors carrying a TP53 mutation; conversely, a wild-type pattern was present in 28 of 30 (93%) tumors without a detectable mutation (p < 0.0001). The majority of BCs with a p53 IHC overexpression pattern (15/17, 88%) contained a missense TP53 mutation; while the majority of BCs with a null pattern (12/14, 86%) contained a truncating mutation (p < 0.0001). The BCs with a null pattern are associated with a high Nottingham histological grade and a triple-negative phenotype when compared to those demonstrating overexpression (p < 0.05).

CONCLUSION:

These findings suggest that p53 IHC can be a potential surrogate for TP53 mutations in BC. Different p53 expression patterns may correlate with specific TP53 genetic mutations in BC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Proteína Supressora de Tumor p53 / Mutação Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: Breast Cancer Res Treat Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Proteína Supressora de Tumor p53 / Mutação Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: Breast Cancer Res Treat Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos