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CHEK2基因敲除是TP53突变型肝细胞癌的一个治疗靶点。

CHEK2 knockout is a therapeutic target for TP53-mutated hepatocellular carcinoma.

作者信息

Chen Yuyan, Zhu Zhengyi, Wu Xingyu, Li Hui, Guan Wenxian, Ren Haozhen

机构信息

Division of Hepatobiliary and Transplantation Surgery, Department of General Surgery, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, 210008, Nanjing, China.

Department of Radiology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, 210008, Nanjing, China.

出版信息

Cell Death Discov. 2024 Jan 19;10(1):37. doi: 10.1038/s41420-023-01777-4.

Abstract

Currently, there is still a lack of novel and effective drug targets to improve the prognosis of hepatocellular carcinoma (HCC). Additionally, the role of CHEK2 in HCC has not been reported yet. The eQTLgen database and two HCC Genome-Wide Association Study (GWAS) datasets (ieu-b-4953, ICD10 C22.0) were used to find the drug target: CHEK2. Next, Colony, Edu, β-gal, and cell cycle analysis were facilitated to evaluate the role of CHEK2 knockout in HCC. In addition, Nultin-3 was added to evaluate the apoptosis of TP53-mutated HCC cells with CHEK2 knockout. Furthermore, MitoSox, electron microscopy, mitochondrial ATP, and NADH+/NADH levels were assessed in the CHEK2 knockout HCC cells with or without Metformin. Finally, cell-derived tumor xenograft was used to evaluate the role of CHEK2 knockout in vivo. We initially identified a potential drug target, CHEK2, through GWAS data analysis. Furthermore, we observed a significant upregulation of CHEK2 expression in HCC, which was found to be correlated with a poor prognosis. Subsequently, the results indicated that knocking out CHEK2 selectively affects the proliferation, cell cycle, senescence, and apoptosis of TP53-mutant HCC cells. Additionally, the introduction of Nultin-3 further intensified the functional impact on TP53-mutant cells. Then ClusterProfiler results showed high CHEK2 and TP53 mutation group was positively enriched in the mitochondrial ATP pathway. Then we used MitoSox, electron microscopy, mitochondrial ATP, and NADH + /NADH assay and found knockout of CHECK could induce the ATP pathway to inhibit the growth of HCC. Our research introduces a novel drug target for TP53-mutant HCC cells via mitochondrial ATP, addressing the limitation of Nultin-3 as a standalone treatment that does not induce tumor cell death.

摘要

目前,仍缺乏改善肝细胞癌(HCC)预后的新型有效药物靶点。此外,CHEK2在HCC中的作用尚未见报道。利用eQTLgen数据库和两个HCC全基因组关联研究(GWAS)数据集(ieu-b-4953,ICD10 C22.0)来寻找药物靶点:CHEK2。接下来,通过集落、Edu、β-半乳糖苷酶和细胞周期分析来评估CHEK2基因敲除在HCC中的作用。此外,添加Nultin-3来评估CHEK2基因敲除的TP53突变型HCC细胞的凋亡情况。此外,对有或没有二甲双胍的CHEK2基因敲除HCC细胞进行MitoSox、电子显微镜、线粒体ATP和NADH+/NADH水平评估。最后,利用细胞衍生的肿瘤异种移植来评估CHEK2基因敲除在体内的作用。我们最初通过GWAS数据分析确定了一个潜在的药物靶点CHEK2。此外,我们观察到HCC中CHEK2表达显著上调,且发现其与预后不良相关。随后,结果表明敲除CHEK2选择性地影响TP53突变型HCC细胞的增殖、细胞周期、衰老和凋亡。此外,引入Nultin-3进一步增强了对TP53突变型细胞的功能影响。然后,ClusterProfiler结果显示CHEK2和TP53高突变组在线粒体ATP途径中呈正富集。然后我们使用MitoSox、电子显微镜、线粒体ATP和NADH + /NADH检测,发现敲除CHECK可诱导ATP途径抑制HCC生长。我们的研究通过线粒体ATP为TP53突变型HCC细胞引入了一种新型药物靶点,解决了Nultin-3作为单一治疗不能诱导肿瘤细胞死亡的局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02e4/10799024/bdba6d744c5c/41420_2023_1777_Fig1_HTML.jpg

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