Chen Yi-Xiao, Guo Yan, Dong Shan-Shan, Chen Xiao-Feng, Chen Jia-Bin, Zhang Yu-Jie, Yao Shi, Thynn Hlaing Nwe, Zhi Liqiang, Yang Tie-Lin
Department of Joint Surgery, Honghui Hospital; The Key Laboratory of Biomedical Information Engineering of Ministry of Education, Xi'an Jiaotong University, Xi'an, P. R. China.
Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an, Shaanxi Province, 710049, P. R. China.
J Cancer. 2018 Oct 5;9(21):3858-3866. doi: 10.7150/jca.22855. eCollection 2018.
Although genome-wide association studies (GWASs) have identified some risk single-nucleotide polymorphisms in East Asian never-smoking females, the unexplained missing heritability is still required to be investigated. Runs of homozygosity (ROHs) are thought to be a type of genetic variation acting on human complex traits and diseases. We detected ROHs in 8,881 East Asian never-smoking women. The summed ROHs were used to fit a logistic regression model which noteworthily revealed a significant association between ROHs and the decreased risk of lung cancer ( < 0.05). We identified 4 common ROHs regions located at 2p22.1, which were significantly associated with decreased risk of lung cancer ( = 2.00 × 10 - 1.35 × 10). Functional annotation was conducted to investigate the regulatory function of ROHs. The common ROHs were overlapped with potential regulatory elements, such as active epigenome elements and chromatin states in lung-derived cell lines. and were significantly up-regulated as the putative target genes of the identified ROHs in lung cancer samples according to the analysis of differently expressed genes. Our results suggest that ROHs could act as recessive contributing factors and regulatory elements to influence the risk of lung cancer in never-smoking East Asian females.
尽管全基因组关联研究(GWASs)已经在东亚从不吸烟女性中鉴定出一些风险单核苷酸多态性,但仍需要对无法解释的遗传力缺失进行研究。纯合子片段(ROHs)被认为是一种作用于人类复杂性状和疾病的遗传变异类型。我们在8881名东亚从不吸烟女性中检测了ROHs。将总的ROHs用于拟合逻辑回归模型,该模型显著揭示了ROHs与肺癌风险降低之间的显著关联(<0.05)。我们确定了位于2p22.1的4个常见ROHs区域,它们与肺癌风险降低显著相关(=2.00×10 - 1.35×10)。进行了功能注释以研究ROHs的调控功能。常见的ROHs与潜在的调控元件重叠,如肺来源细胞系中的活性表观基因组元件和染色质状态。根据差异表达基因分析,和作为所鉴定的ROHs在肺癌样本中的假定靶基因显著上调。我们的结果表明,ROHs可能作为隐性促成因素和调控元件影响东亚从不吸烟女性患肺癌的风险。