Integrated analysis of genes encoding ATP-dependent chromatin remodellers identifies CHD7 as a potential target for colorectal cancer therapy

被引：4

作者：

Zhang, Xingyan ^{[1
]}

Zhou, Yaoyao ^{[2
]}

Shi, Zhenyu ^{[2
]}

Liu, Zhenfeng ^{[1
]}

Chen, Hao ^{[1
]}

Wang, Xiaochen ^{[1
]}

Cheng, Yiming ^{[1
]}

Xi, Lishan ^{[1
]}

Li, Xuanyuan ^{[1
]}

Zhang, Chunze ^{[3
]}

Bao, Li ^{[2
]}

Xuan, Chenghao ^{[1
]}

机构：

[1] Tianjin Med Univ, Key Lab Immune Microenvironm & Dis, Prov & Minist Cosponsored Collaborat Innovat Ctr, Minist Educ,Dept Biochem & Mol Biol, Tianjin, Peoples R China

[2] Tianjin Med Univ, Key Lab Breast Canc Prevent & Therapy,Minist Educ, Tianjin Med Univ Canc Inst & Hosp,Tianjins Clin R, Natl Clin Res Ctr Canc,Key Lab Canc Prevent & The, Tianjin, Peoples R China

[3] Tianjin Union Med Ctr, Dept Colorectal Surg, Tianjin Inst Coloproctol, Tianjin, Peoples R China

来源：

CLINICAL AND TRANSLATIONAL MEDICINE | 2022年 / 12卷 / 07期

基金：

中国国家自然科学基金;

关键词：

SOMATIC POINT MUTATIONS; ADENYLATE KINASE; COMPLEX; GENOME; P53; PHOSPHORYLATION; DISCOVERY; FAMILY;

D O I：

10.1002/ctm2.953

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Background Genes participating in chromatin organization and regulation are frequently mutated or dysregulated in cancers. ATP-dependent chromatin remodelers (ATPCRs) play a key role in organizing genomic DNA within chromatin, therefore regulating gene expression. The oncogenic role of ATPCRs and the mechanism involved remains unclear. Methods We analyzed the genomic and transcriptional aberrations of the genes encoding ATPCRs in The Cancer Genome Atlas (TCGA) cohort. A series of cellular experiments and mouse tumor-bearing experiments were conducted to reveal the regulatory function of CHD7 on the growth of colorectal cancer cells. RNA-seq and ATAC-seq approaches together with ChIP assays were performed to elucidate the downstream targets and the molecular mechanisms. Results Our data showed that many ATPCRs represented a high frequency of somatic copy number alterations, widespread somatic mutations, remarkable expression abnormalities, and significant correlation with overall survival, suggesting several somatic driver candidates including chromodomain helicase DNA-binding protein 7 (CHD7) in colorectal cancer. We experimentally demonstrated that CHD7 promotes the growth of colorectal cancer cells in vitro and in vivo. CHD7 can bind to the promoters of target genes to maintain chromatin accessibility and facilitate transcription. We found that CHD7 knockdown downregulates AK4 expression and activates AMPK phosphorylation, thereby promoting the phosphorylation and stability of p53 and leading to the inhibition of the colorectal cancer growth. Our muti-omics analyses of ATPCRs across large-scale cancer specimens identified potential therapeutic targets and our experimental studies revealed a novel CHD7-AK4-AMPK-p53 axis that plays an oncogenic role in colorectal cancer.

引用

页数：19