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1.
In Vivo ; 18(6): 703-11, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15646810

RESUMEN

Short-term cultures of fifty-two samples of fibroadenomas were cytogenetically analyzed. Thirty-three of the successfully karyotyped fibroadenomas were further investigated for the presence of amplifications in the CCND1, c-MYC and HER/2-neu genes by means of FISH analysis. Compared to carcinomas, fibroadenomas seem to have less complex cytogenetic rearrangements and limited alterations on HER-2/neu, CCND1 and c-MYC loci. A cytogenetic subgroup of fibroadenomas with hyperdiploid karyotypes and only numerical changes was observed. Amplification of CCND1 seems to play a more substantial role in benign tumor progression. These findings confirm that fibroadenomas do have genetic alterations and support the hypothesis that a fibroadenoma subset displays changes also found in carcinomas, thus indicating that patients belonging to this group might have an increased risk for subsequent breast cancer.


Asunto(s)
Neoplasias de la Mama/genética , Aberraciones Cromosómicas/clasificación , Fibroadenoma/genética , Cariotipificación Espectral/métodos , Aneuploidia , Neoplasias de la Mama/patología , Carcinoma/genética , Carcinoma/patología , ADN de Neoplasias/análisis , Femenino , Fibroadenoma/patología , Humanos , Interfase/genética , Metafase/genética , Reacción en Cadena de la Polimerasa/métodos , Células Tumorales Cultivadas
2.
Thromb Haemost ; 105(1): 131-7, 2011 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-21057706

RESUMEN

Human kallikrein-related peptidase 14 gene (KLK14) is regulated by androgens and progestins. This gene is expressed in the central nervous system and endocrine tissues such as the breast, prostate and ovary. The differential KLK14 mRNA expression levels are related to several human neoplasias, among them breast cancer. The aim of this study was to analyse the KLK14 expression in breast tissues and to investigate its differential diagnostic and prognostic value in the mammary carcinomas. For this purpose, we isolated total RNA from 70 malignant and 33 benign specimens. After testing RNA quality, we synthesised cDNA by reverse transcription and applied a highly sensitive quantitative real-time PCR (qRT-PCR) method for KLK14 mRNA quantification using the SYBR Green® chemistry. HPRT1 was used as a reference gene and the BT20 breast cancer cell line as a calibrator. Relative quantification analysis was performed using the comparative CT method 2-ΔΔCT. KLK14 expression was detected in both types of breast tumours. However, a statistically significant increase of the KLK14 mRNA level was observed in the malignant, compared to the benign tumour samples (p<0.001), highlighting its value in discriminating these breast lesions. Elevated KLK14 expression profiles were associated with higher tumour grade (p=0.043) and size (p=0.007) in cancerous samples. Furthermore, KLK14 mRNA expression showed negative correlation in a statistically significant manner with estrogen receptor status (p=0.024). In accordance with logistic regression models (p=0.012) and receiver-operating-characteristics analysis (p<0.001), KLK14 gene expression could be evaluated as a putative independent diagnostic biomarker in breast tumour biopsies.


Asunto(s)
Biomarcadores de Tumor/análisis , Neoplasias de la Mama/diagnóstico , Calicreínas/análisis , Biopsia , ADN Complementario , Femenino , Humanos , Modelos Logísticos , Proteínas de Neoplasias/análisis , ARN Mensajero/análisis , Curva ROC , Receptores de Estrógenos/análisis
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