组蛋白甲基转移酶
EZH2型
表观遗传学
细胞生长
PRC2
细胞
甲基转移酶
增强子
免疫组织化学
癌症研究
生物
基因
甲基化
基因表达
遗传学
免疫学
作者
Min Shi,Ali Shahsafaei,Cuiling Liu,Hongbo Yu,David M. Dorfman
标识
DOI:10.3109/10428194.2014.968780
摘要
Enhancer of zeste homolog 2 (EZH2), an epigenetic regulator and H3k27-specific histone methyltransferase, is important for transcriptional regulation. EZH2 has been found to be overexpressed in B-cell lymphomas, as well as some T-cell lymphomas. Here we investigated the expression of EZH2 by immunohistochemical staining in a wide range of T-cell neoplasms. We found that EZH2 is highly expressed in all categories of T-cell neoplasia studied, and its expression strongly correlates with a high proliferation rate. Although up-regulation of EZH2 has been reported to be modulated by the pSTAT3-MYC pathway, our data indicate that EZH2 expression is correlated with MYC and/or pSTAT3 expression in only a subset of T-cell lymphomas, and that other mechanisms may control the overexpression of EZH2 in many T-cell lymphomas. The high level of EZH2 expression in T cell lymphomas suggest that these neoplasms may benefit from targeted treatment with a small molecule inhibitor of EZH2 currently in use in clinical trials.
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