EZH2型
BCL6公司
癌症研究
弥漫性大B细胞淋巴瘤
生发中心
细胞生长
淋巴瘤
生物
脱甲基剂
下调和上调
B细胞
DNA甲基化
免疫学
甲基化
遗传学
基因
基因表达
抗体
作者
Panjun Wang,Longjiang Xu,Yinyin Fan,Bing-Zong Li,Jiang Li,Xiaohui Zhang,Yu Sun,Jinxiang Fu
标识
DOI:10.1080/10428194.2022.2131411
摘要
Diffuse large B-cell lymphomas (DLBCLs) are phenotypically and genetically heterogeneous. Two main subgroups of DLBCL include germinal center B-cell-like (GCB) and activated B-cell-like (ABC). Molecular profiling can further classify DLBCL into four subtypes: MCD (both CD79B and MYD88 L265P), BN2 (NOTCH2 mutation or BCL6 fusion), N1 (NOTCH1 mutation), or EZB (EZH2 mutation or BCL2 fusion). EZH2 inhibitors were recommended for patients with the EZB subtype of DLBCLs; however, little is known about the therapeutic mechanisms. Our results showed that DZNep arrested G1/S phase of GCB-DLBCL cells and inhibited the cell proliferation in vitro through upregulation of p16 by demethylating its promoter. These results suggest that DZNep may have potential as a novel therapeutic agent for DFLBL therapy. This agent may serve as a novel molecular agent to be applied to GCB DLBCL.
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