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J Clin Pathol ; 69(10): 858-65, 2016 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-27056456

RESUMO

AIMS: Recent reports have identified recurrent MED12 somatic mutations in fibroadenomas and phyllodes tumours. The frequency and type of somatic mutations were noted to be similar to those of uterine leiomyomas. We aimed to investigate protein expression of MED12, correlating it to MED12 mutational status and expression of oestrogen receptors (ER). METHODS: Immunohistochemistry was performed on a total of 232 fibroepithelial lesions (100 fibroadenomas, 132 phyllodes tumours) diagnosed at the Department of Pathology, Singapore General Hospital using MED12, ERα and ERß antibodies. Expressions were evaluated in both stroma and epithelium, and correlated with MED12 mutational status. RESULTS: MED12 mutation was significantly associated with high MED12 protein expression (H-score >150) in the stroma (p=0.029), but not in the epithelium. It was not associated with ERα and ERß protein expression in both stroma and epithelium. MED12 protein expression was significantly correlated with ERα in epithelial (p=0.007) and ERß in stromal (p=0.049) components. MED12 was not significantly different between fibroadenomas and phyllodes tumours. Epithelial expression of ERα was significantly higher in fibroadenomas (p<0.001) than in phyllodes tumours. Conversely, both epithelial and stromal expression of ERß was significantly higher in phyllodes tumours (p<0.001). CONCLUSIONS: Positive associations observed between MED12 and ERα, ERß immunohistochemical expression suggest a biological interplay between the proteins. The lack of significant association of MED12 mutation with ER protein expression indicates a need to further explore the functional impact of MED12 mutations on the ER signalling pathway in breast fibroepithelial lesions.


Assuntos
Neoplasias da Mama/genética , Fibroadenoma/genética , Complexo Mediador/genética , Tumor Filoide/genética , Receptores de Estrogênio/metabolismo , Adolescente , Adulto , Idoso , Neoplasias da Mama/diagnóstico , Estudos de Coortes , Análise Mutacional de DNA , Receptor alfa de Estrogênio/genética , Receptor alfa de Estrogênio/metabolismo , Receptor beta de Estrogênio/genética , Receptor beta de Estrogênio/metabolismo , Estrogênios/metabolismo , Feminino , Fibroadenoma/diagnóstico , Regulação Neoplásica da Expressão Gênica , Sequenciamento de Nucleotídeos em Larga Escala , Humanos , Complexo Mediador/metabolismo , Pessoa de Meia-Idade , Mutação , Tumor Filoide/diagnóstico , Receptores de Estrogênio/genética , Singapura , Adulto Jovem
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