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靶向 ZNF334 启动子的 DNA 去甲基化抑制结直肠癌生长。

Targeted DNA demethylation of the ZNF334 promoter inhibits colorectal cancer growth.

机构信息

School of Pharmacy, Southwest Minzu University, Chengdu, 610225, Sichuan, China.

BMI Center for Biomass Materials and Nanointerfaces, College of Biomass Science and Engineering, Sichuan University, Chengdu, 610065, Sichuan, China.

出版信息

Cell Death Dis. 2023 Mar 25;14(3):210. doi: 10.1038/s41419-023-05743-x.

Abstract

Colorectal cancer (CRC) is a leading cause of cancer deaths worldwide. Aberrant regulation of DNA methylation in promoters of tumor suppressor genes or proto-oncogenes is one of the fundamental processes driving the initiation and progression of CRC. Zinc-finger proteins (ZNFs) are one of the most abundant groups of proteins and function in many important biological processes related to tumorigenesis. Herein, we detected abnormal hypermethylation of the ZNF334 gene in CRC tissues compared with normal tissues, and this modification downregulated the expression of ZNF334. Furthermore, ten-eleven translocation 1 (TET1) was identified to be involved in regulating the methylation level of ZNF334. Next, a dCas9-multiGCN4/scFv-TET1CD-sgZNF334-targeted demethylation system was constructed to reverse the expression of ZNF334 through sgRNA targeting the ZNF334 promoter. Both in vitro and in vivo experiments demonstrated the targeted demethylation system upregulated ZNF334 expression and inhibited CRC growth. Collectively, targeted DNA demethylation of the ZNF334 promoter sheds light on the precise treatment of CRC.

摘要

结直肠癌(CRC)是全球癌症死亡的主要原因。肿瘤抑制基因或原癌基因启动子中 DNA 甲基化的异常调节是驱动 CRC 发生和进展的基本过程之一。锌指蛋白(ZNFs)是最丰富的蛋白之一,在与肿瘤发生相关的许多重要生物学过程中发挥作用。在此,我们检测到 CRC 组织中 ZNF334 基因的异常高甲基化,这种修饰下调了 ZNF334 的表达。此外,鉴定出 ten-eleven translocation 1(TET1)参与调节 ZNF334 的甲基化水平。接下来,构建了 dCas9-multiGCN4/scFv-TET1CD-sgZNF334 靶向去甲基化系统,通过靶向 ZNF334 启动子的 sgRNA 逆转 ZNF334 的表达。体外和体内实验均表明靶向去甲基化系统上调 ZNF334 表达并抑制 CRC 生长。总之,ZNF334 启动子的靶向 DNA 去甲基化为 CRC 的精确治疗提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99a6/10039945/784a54442207/41419_2023_5743_Fig1_HTML.jpg

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