Clustering of Cancer Cell Lines Using A Promoter- Targeted Liquid Hybridization Capture-Based Bisulfite Sequencing Approach

被引:7
|
作者
Gao, Fei [1 ]
Wang, Junwen [1 ]
Ji, Guanyu [1 ]
Liu, Siyang [1 ]
Yao, Yu [1 ]
Wang, Tong [1 ]
Wu, Honglong [1 ]
Xia, Yudong [1 ]
Gong, Desheng [1 ]
Jiang, Hui [1 ]
Yang, Huanming [1 ,2 ,3 ]
Zhang, Xiuqing [4 ]
机构
[1] BGI Shenzhen, Sci & Technol Dept, Shenzhen 518083, Peoples R China
[2] King Abdulaziz Univ, Jeddah 21413, Saudi Arabia
[3] James D Watson Inst Genome Sci, Hangzhou, Zhejiang, Peoples R China
[4] BGI Shenzhen, Guangdong Enterprise Key Lab Human Dis Genom, Shenzhen 518083, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
Cancer classification; CIMP; DNA methylation; Promoter; Targeted bisulfite sequencing; ISLAND METHYLATOR PHENOTYPE; GENOME-WIDE ANALYSIS; DNA METHYLATION; GENE-EXPRESSION; CPG ISLANDS; CLASSIFICATION; HYPERMETHYLATION; 5-HYDROXYMETHYLCYTOSINE; 5-METHYLCYTOSINE; PREDICTION;
D O I
10.1177/1533034614500416
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
DNA methylation plays a significant role in assuring cell identity, thus potentiating its application in molecular classification of cancers in respect to tissue-origins or clinically and etiologically distinct subtypes. In this study, we optimized our liquid hybridization capture-based bisulfite sequencing (LHC-BS) approach on the gene promoter regions of 11 cell lines. Our results indicated that promoter methylomes could not only cluster cancer cell lines with respect to tissue origins but also differentiate cancer subtypes based on CpG island methylator phenotype (CIMP). Promoter-targeted LHC-BS as means for comprehensive screening and classifying cancer cells with promoter methylomes provided a powerful strategy for further complex clinical studies.
引用
收藏
页码:383 / 394
页数:12
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