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1.
Int J Gynecol Cancer ; 15(6): 1081-8, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-16343185

RESUMEN

Fragile histidine triad (FHIT), a candidate of tumor suppressor protein, expression was examined on paraffin-embedded specimens in proliferative, secretory, hyperplastic, and neoplastic human endometrium by immunohistochemistry. The results of FHIT immunoreactivity in endometrial carcinomas were compared with prognostic indicators as well as with p53 overexpression. Forty-four cases of endometrial carcinoma, 30 normal functional (15 proliferative, 15 secretory), and 24 hyperplastic endometrium (12 without atypia, 12 with atypia) specimens were studied using polyclonal FHIT antibody. The streptavidin-biotin-peroxidase detection system was used, and the intensity and the distribution of immunoreactivity were evaluated semiquantitatively. There were no significant differences in FHIT expression in the proliferative, secretory, hyperplastic, either with or without atypia, or carcinomatous endometria. No significant difference in FHIT expression of endometrial carcinomas was detected when prognostic parameters or p53 overexpression were considered. Loss or reduced FHIT expression was not found to predict disease-free or cumulative survivals. This study showed that loss or reduction in FHIT protein expression is present in normal functional and hyperplastic endometria as well as in neoplastic endometrium. FHIT protein seems not to be involved directly in endometrial carcinogenesis, but rather, it regulates cell proliferation both in physiologic and in pathologic conditions of endometrium.


Asunto(s)
Ácido Anhídrido Hidrolasas/biosíntesis , Adenocarcinoma/metabolismo , Neoplasias Endometriales/metabolismo , Endometrio/metabolismo , Proteínas de Neoplasias/biosíntesis , Adenocarcinoma/patología , Adenocarcinoma/fisiopatología , Adulto , Anciano , Anciano de 80 o más Años , Proliferación Celular , Neoplasias Endometriales/patología , Neoplasias Endometriales/fisiopatología , Endometrio/patología , Endometrio/fisiología , Endometrio/fisiopatología , Femenino , Humanos , Hiperplasia/metabolismo , Hiperplasia/fisiopatología , Persona de Mediana Edad , Análisis de Supervivencia , Proteína p53 Supresora de Tumor/biosíntesis
2.
J Clin Pathol ; 56(7): 552-4, 2003 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12835305

RESUMEN

Glycogen rich clear cell carcinoma of the breast is a rare neoplasm with different morphological characteristics to ordinary breast carcinomas. However, it has some common features with clear cell carcinomas of other organs. This report describes a case of clear cell carcinoma of the breast with a solid papillary pattern centrally localised in the left breast of a 45 year old woman. Antibodies directed against cytokeratin 7 (CK7), CK10, CK14, CK17, CK18, CK19, CK20, CK5/6/18, CK8/18, high molecular weight cytokeratin AE3, high molecular weight cytokeratin 34betaE12, the oestrogen receptor, the progesterone receptor, chromogranin, S-100 protein, smooth muscle actin, vimentin, and carcinoembryogenic antigen were applied to analyse the immunophenotypical profile of this rare neoplasm.


Asunto(s)
Adenocarcinoma de Células Claras/patología , Neoplasias de la Mama/patología , Adenocarcinoma de Células Claras/química , Adenocarcinoma de Células Claras/inmunología , Antígenos CD/análisis , Neoplasias de la Mama/química , Neoplasias de la Mama/inmunología , Citoplasma/química , Femenino , Glucógeno/análisis , Histocitoquímica , Humanos , Inmunohistoquímica , Queratinas/análisis , Persona de Mediana Edad , Vimentina/análisis
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