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Pathol Oncol Res ; 17(3): 627-32, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21267686

RESUMO

Intratumoral biosynthesis of hormone steroids is thought to play a role in the pathogenesis and development of human breast cancer. There is evidence that glucocorticoids may inhibit the development and progression of breast cancer. 11ß-hydroxysteroid dehydrogenase (11ß-HSD) type 1 is the enzyme which converts inactive cortisone to active cortisol. In order to study the expression of 11ß-HSD type 1 in breast cancer and non-cancerous breast tissue, we have developed specific antibodies to 11ß-HSD type 1 and proceeded to localization of the enzyme in 84 specimens of breast carcinoma and adjacent non-malignant tissues by immnohistochemistry. The results were correlated with the expression of androgen receptor, estrogen receptor, progesterone receptor, glucocorticoid receptor and CDC47, a cell division marker, as well as the tumor stage, tumor size, nodal status and menopausal status. The expression of 11ß-HSD type 1 in 64% of breast cancer specimens appeared significantly lower than that observed in normal adjacent tissues (97% of cases being positive). There was no significant correlation between 11ß-HSD type 1 expression and the clinicopathological parameters studied. The decrease in 11ß-HSD type 1 expression in breast cancer as compared to that observed in the adjacent normal tissues may play a role in the development and/or progression of the cancer by modifying the intratumoral levels of glucocorticoids.


Assuntos
11-beta-Hidroxiesteroide Desidrogenase Tipo 1/metabolismo , Biomarcadores Tumorais/metabolismo , Neoplasias da Mama/metabolismo , Mama/metabolismo , Adulto , Idoso , Mama/patologia , Neoplasias da Mama/patologia , Proteínas de Ciclo Celular/metabolismo , Proteínas de Ligação a DNA/metabolismo , Receptor alfa de Estrogênio/metabolismo , Feminino , Humanos , Técnicas Imunoenzimáticas , Pessoa de Meia-Idade , Componente 7 do Complexo de Manutenção de Minicromossomo , Proteínas Nucleares/metabolismo , Prognóstico , Receptores Androgênicos/metabolismo , Receptores de Glucocorticoides/metabolismo , Receptores de Progesterona/metabolismo
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