Identification and characteristic analysis of enhancers across 13 major cancer types.

IF 5.1 4区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Precision Clinical Medicine Pub Date : 2021-08-02 eCollection Date: 2021-09-01 DOI:10.1093/pcmedi/pbab019
Mingming Qian, Wenzhu Wang, Yana Zhang, Yi Zhao, Huige Quan, Yuting Chen, Xinyue Dai, Zhiyun Guo
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引用次数: 0

Abstract

Enhancers are often mutated and dysregulated in various diseases such as cancer. By integrating the function annotation of the mammalian genome (FANTOM) enhancers expression profiles and RNA-seq data from The Cancer Genome Atlas (TCGA) of 13 cancers and their corresponding para-cancerous tissues, we systematically identified a total of 4702 significantly differentially expressed (DE) enhancers. Furthermore, a total of 1036 DE genes regulated by DE enhancers were identified. It was found that in these 13 cancers, most (61.13%) enhancers were ubiquitously expressed, whereas DE enhancers were more likely to be tissue-specific expressed, and the DE genes regulated by DE enhancers were significantly enriched in cancer-related pathways. Finally, it was manifested that 74 single nucleotide polymorphisms (SNPs) were located in 37 DE enhancers, and these SNPs affected the gain and loss of functional transcription factor binding sites of 758 transcription factors, which were shown to be highly correlated with tumorigenesis and development.

对 13 种主要癌症类型的增强子进行识别和特征分析。
增强子在癌症等各种疾病中经常发生突变和失调。通过整合哺乳动物基因组(FANTOM)增强子表达谱的功能注释和来自癌症基因组图谱(TCGA)的13种癌症及其相应癌旁组织的RNA-seq数据,我们系统地鉴定了4702个显著差异表达(DE)的增强子。此外,我们还发现了1036个受DE增强子调控的DE基因。研究发现,在这13种癌症中,大多数(61.13%)增强子是泛在表达的,而DE增强子更有可能是组织特异性表达的,而且由DE增强子调控的DE基因在癌症相关通路中明显富集。最后,研究表明,有74个单核苷酸多态性(SNPs)位于37个DE增强子中,这些SNPs影响了758个转录因子功能结合位点的获得和丢失,而这些位点与肿瘤的发生和发展高度相关。
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来源期刊
Precision Clinical Medicine
Precision Clinical Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
10.80
自引率
0.00%
发文量
26
审稿时长
5 weeks
期刊介绍: Precision Clinical Medicine (PCM) is an international, peer-reviewed, open access journal that provides timely publication of original research articles, case reports, reviews, editorials, and perspectives across the spectrum of precision medicine. The journal's mission is to deliver new theories, methods, and evidence that enhance disease diagnosis, treatment, prevention, and prognosis, thereby establishing a vital communication platform for clinicians and researchers that has the potential to transform medical practice. PCM encompasses all facets of precision medicine, which involves personalized approaches to diagnosis, treatment, and prevention, tailored to individual patients or patient subgroups based on their unique genetic, phenotypic, or psychosocial profiles. The clinical conditions addressed by the journal include a wide range of areas such as cancer, infectious diseases, inherited diseases, complex diseases, and rare diseases.
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