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19q13 KRAB 锌指蛋白 ZNF471 通过激活 MAPK10/JNK3 信号通路,但在食管癌中常因启动子 CpG 甲基化而失活。

19q13 KRAB zinc-finger protein ZNF471 activates MAPK10/JNK3 signaling but is frequently silenced by promoter CpG methylation in esophageal cancer.

机构信息

Key Laboratory of Molecular Oncology and Epigenetics, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

Cancer Epigenetics Laboratory, Department of Clinical Oncology, State Key Laboratory of Translational Oncology, Sir YK Pao Center for Cancer and Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong and CUHK-Shenzhen Research Institute, Hong Kong.

出版信息

Theranostics. 2020 Jan 12;10(5):2243-2259. doi: 10.7150/thno.35861. eCollection 2020.

DOI:10.7150/thno.35861
PMID:32089740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7019175/
Abstract

Zinc-finger proteins (ZFPs) are the largest transcription factor family in mammals, involved in the regulation of multiple physiologic processes including cell differentiation, proliferation, apoptosis and neoplastic transformation. Approximately one-third of ZFPs are Krüppel-associated box domain (KRAB)-ZFPs. : ZNF471 expression and methylation were detected by reverse-transcription PCR and methylation-specific PCR. The impact and mechanism of ectopic ZNF471 expression in esophageal squamous cell carcinoma (ESCC) cells was evaluated in vitro and in vivo. : We identified a 19q13 KRAB-ZFP, , as a methylated target in ESCC. We further found that ZNF471 is significantly downregulated in ESCC tissues compared with adjacent non-cancer tissues, due to its aberrant promoter CpG methylation, and further confirmed by methylation analysis and treatment with demethylation agent. Restoration of ZNF471 expression in silenced ESCC cells significantly altered cell morphology, induced apoptosis and G0/G1 arrest, and inhibited tumor cell colony formation, viability, migration and invasion. Importantly, ZNF471 was found to activate the expression of and family genes, and further enhance MAPK10 signaling and downstream gene expression through binding to the promoter. : Our results demonstrate that ZNF471 is an important tumor suppressor and loss of ZNF471 functions hampers signaling during esophageal carcinogenesis.

摘要

锌指蛋白(ZFP)是哺乳动物中最大的转录因子家族,参与调节多种生理过程,包括细胞分化、增殖、凋亡和肿瘤转化。大约三分之一的 ZFP 是 KRAB 相关盒域(KRAB)-ZFP。:通过逆转录 PCR 和甲基化特异性 PCR 检测 ZNF471 的表达和甲基化。在体外和体内评估了食管鳞状细胞癌(ESCC)细胞中异位 ZNF471 表达的影响和机制。:我们确定了一个 19q13 KRAB-ZFP, ,作为 ESCC 的甲基化靶标。我们进一步发现,ZNF471 在 ESCC 组织中的表达明显低于相邻的非癌组织,这是由于其启动子 CpG 甲基化异常所致,并通过甲基化分析和去甲基化剂处理进一步证实。沉默 ESCC 细胞中 ZNF471 的表达显著改变细胞形态,诱导细胞凋亡和 G0/G1 期阻滞,并抑制肿瘤细胞集落形成、活力、迁移和侵袭。重要的是,ZNF471 被发现可激活 和 家族基因的表达,并通过结合 启动子进一步增强 MAPK10 信号和下游基因表达。:我们的研究结果表明,ZNF471 是一种重要的肿瘤抑制因子,ZNF471 功能的丧失会阻碍食管癌变过程中的 信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0dc/7019175/3a648449afb3/thnov10p2243g008.jpg
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