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Expression of enhancer of zeste homolog2 in colorectal adenocarcinoma and its significance / 肿瘤研究与临床
Cancer Research and Clinic ; (6): 15-18, 2015.
Article de Zh | WPRIM | ID: wpr-473106
Bibliothèque responsable: WPRO
ABSTRACT
Objective To investigate the expression of the enhancer of zeste homolog 2 (EZH2) gene and its significance in colorectal adenocarcinoma.Methods Immunohistochemistry and Western blot was used to assess the expression of EZH2 in human colorectal adenocarcinoma tissues,colorectal adenoma tissues and non-cancerous adjacent colorectal tissues.The relationships between EZH2 and each clinical pathology parameter were analyzed.Results The results of immunohistochemical trail showed that the expression rates of EZH2 in colorectal adenocarcinoma,colorectal adenoma and non-cancerous adjacent colorectal tissues were 80.56 % (87/108),62.5 % (25/40) and 5.00 % (2/40),respectively (P < 0.05).Western blot revealed that the expression level of EZH2 in colorectal adenocarcinoma tissues,colorectal adenoma tissues and non-cancerous adjacent colorectal tissues level 0.549±0.145,0.283±0.023 and 0.107±0.022,respectively.The level in colorectal adenocarcinoma tissues (0.549±0.145) and colorectal adenoma (0.283±0.023) was significantly higher than that in non-cancerous adjacent colorectal tissues (0.107±0.022).Compared with colorectal adenoma tissues,level in colorectal adenocarcinoma tissues was significantly higher.There were significant differences among the three groups (F =20.113,P < 0.05).The ratio of high expression level of EZH2 in colorectal adenocarcinoma tissues was closed related with tumorgenesis,differentiation,TNM staging and lymphatic metastsis (all P < 0.05).However,no correlation was revealed between EZH2 expression and the age,gender (both P > 0.05).Conclusion The expression of EZH2 may be associated with the tumorgenesis invasion,metastasis and progression of colorectal adenocarcinoma.
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Texte intégral: 1 Indice: WPRIM langue: Zh Texte intégral: Cancer Research and Clinic Année: 2015 Type: Article
Texte intégral: 1 Indice: WPRIM langue: Zh Texte intégral: Cancer Research and Clinic Année: 2015 Type: Article