A Diagnostic Panel of DNA Methylation Biomarkers for Lung Adenocarcinoma

被引:31
作者
Shen, Nan [1 ,2 ,5 ]
Du, Jun [3 ]
Zhou, Hui [4 ]
Chen, Nan [5 ]
Pan, Yi [6 ,7 ]
Hoheisel, Jorg D. [6 ]
Jiang, Zonghui [8 ]
Xiao, Ling [9 ]
Tao, Yue [2 ]
Mo, Xi [2 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Childrens Med Ctr, Dept Infect Dis, Sch Med, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Childrens Med Ctr, Pediat Translat Med Inst, Sch Med, Shanghai, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Shanghai Childrens Med Ctr, Diagnost Imaging Ctr, Shanghai, Peoples R China
[4] Cent South Univ, Xiangya Sch Med, Tumor Hosp, Lymphoma & Hematol Dept, Changsha, Hunan, Peoples R China
[5] Shanghai Jiao Tong Univ, Chongming Branch, Sch Med, Xinhua Hosp, Shanghai, Peoples R China
[6] German Canc Res Ctr, Div Funct Genome Anal, Heidelberg, Germany
[7] Heidelberg Univ, Fac Med Heidelberg, Heidelberg, Germany
[8] First Peoples Hosp, Dept Med Oncol, Chuzhou, Peoples R China
[9] Cent South Univ, Sch Basic Med Sci, Dept Histol & Embryol, Changsha, Hunan, Peoples R China
基金
芬兰科学院;
关键词
lung adenocarcinoma; DNA methylation; random forest; HOXA9; KRTAP8-1; CCND1; TULP2; biomarker; CANCER PATIENTS; HYPERMETHYLATION; EXPRESSION; PROFILES; PLASMA; GENES;
D O I
10.3389/fonc.2019.01281
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung adenocarcinoma (LUAD) is one of the most common cancers and lethal diseases in the world. Recognition of the undetermined lung nodules at an early stage is useful for a favorable prognosis. However, there is no good method to identify the undetermined lung nodules and predict their clinical outcome. DNA methylation alteration is frequently observed in LUAD and may play important roles in carcinogenesis, diagnosis, and prediction. This study took advantage of publicly available methylation profiling resources and a machine learning method to investigate methylation differences between LUAD and adjacent non-malignant tissue. The prediction panel was first constructed using 338 tissue samples from LUAD patients including 149 non-malignant ones. This model was then validated with data from The Cancer Genome Atlas database and clinic samples. As a result, the methylation status of four CpG loci in homeobox A9 (HOXA9), keratin-associated protein 8-1 (KRTAP8-1), cyclin D1 (CCND1), and tubby-like protein 2 (TULP2) were highlighted as informative markers. A random forest classification model with an accuracy of 94.57% and kappa of 88.96% was obtained. To evaluate this panel for LUAD, the methylation levels of four CpG loci in HOXA9, KRTAP8-1, CCND1, and TULP2 of tumor samples and matched adjacent lung samples from 25 patients with LUAD were tested. In these LUAD patients, the methylation of HOXA9 was significantly upregulated, whereas the methylation of KRTAP8-1, CCND1, and TULP2 were downregulated obviously in tumor samples compared with adjacent tissues. Our study demonstrates that the methylation of HOXA9, KRTAP8-1, CCND1, and TULP2 has great potential for the early recognition of LUAD in the undetermined lung nodules. The findings also exhibit that the application of improved mathematic algorithms can yield accurate and particularly robust and widely applicable marker panels. This approach could greatly facilitate the discovery process of biomarkers in various fields.
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页数:9
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