Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Más filtros

Bases de datos
Tipo del documento
Asunto de la revista
País de afiliación
Intervalo de año de publicación
1.
Tumour Biol ; 37(3): 3071-80, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26423403

RESUMEN

Colorectal adenomatous polyp (CRAP) is a major risk factor for the development of sporadic colorectal cancer (CRC). Histone modifications are one of the epigenetic mechanisms that may have key roles in the carcinogenesis of CRC. The objective of the present study is to investigate the alternations in the defined histone modification gene expression profiles in patients with CRAP and CRC. Histone modification enzyme key gene expressions of the CRC, CRAP, and control groups were evaluated and compared using the reverse transcription PCR (RT-PCR) array method. Gene expression analysis was performed in the CRAP group after dividing the patients into subgroups according to the polyp diameter, pathological results, and morphological parameters which are risk factors for developing CRC in patients with CRAP. PAK1, NEK6, AURKA, AURKB, HDAC1, and HDAC7 were significantly more overexpressed in CRC subjects compared to the controls (p < 0.05). PAK1, NEK6, AURKA, AURKB, and HDAC1 were significantly more overexpressed in the CRAP group compared to the controls (p < 0.005). There were no significant differences between the CRAP and CRC groups with regards to PAK1, NEK6, AURKA, or AURKB gene overexpression. PAK1, NEK6, AURKA, and AURKB were significantly in correlation with the polyp diameter as they were more overexpressed in polyps with larger diameters. In conclusion, overexpressions of NEK6, AURKA, AURKB, and PAK1 genes can be used as predictive markers to decide the colonoscopic surveillance intervals after the polypectomy procedure especially in polyps with larger diameters.


Asunto(s)
Adenocarcinoma/genética , Poliposis Adenomatosa del Colon/genética , Aurora Quinasa A/genética , Aurora Quinasa B/genética , Neoplasias Colorrectales/genética , Quinasas p21 Activadas/genética , Adenocarcinoma/patología , Poliposis Adenomatosa del Colon/patología , Adulto , Anciano , Aurora Quinasa A/fisiología , Aurora Quinasa B/fisiología , Neoplasias Colorrectales/patología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Quinasas Relacionadas con NIMA/genética , Quinasas Relacionadas con NIMA/fisiología , Quinasas p21 Activadas/fisiología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA