Identification of specific DNA methylation sites on the Y-chromosome as biomarker in prostate cancer

被引:16
|
作者
Yao, Lushuai [1 ,2 ]
Ren, Shancheng [3 ]
Zhang, Minjie [1 ,2 ]
Du, Fengxia [1 ]
Zhu, Yasheng [3 ]
Yu, Hui [1 ,2 ]
Zhang, Chenyu [1 ]
Li, Xiaohua [1 ]
Yang, Caiyun [1 ]
Liu, Huixian [1 ]
Wang, Dong [1 ,2 ]
Meng, Hao [1 ,2 ]
Chang, Shuang [1 ,2 ]
Han, Xiao [1 ,2 ]
Sun, Yinghao [3 ]
Sun, Yingli [1 ]
机构
[1] Chinese Acad Sci, Beijing Inst Genom, Key Lab Genom & Precis Med, Beijing, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
[3] Second Mil Med Univ, Shanghai Changhai Hosp, Dept Urol, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA methylation; prostate cancer; Y-chromosome; biomarker; MORTALITY; MARKERS; RISK;
D O I
10.18632/oncotarget.6141
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
As a diagnostic biomarker, prostate special antigen (PSA) tests always generate false positive results and lead to unnecessary and/or repeat biopsies. Therefore, there is an urgent need for developing more sensitive, specific diagnostic biomarkers. We epigenotyped methylated sites in cancer tissues and adjacent normal tissues from 66 patients. In comparation with normal adjacent tissues, we observed that there were 6 aberrant methylation sites in prostate cancer tissues on the Y-chromosome. We further performed pyrosequencing using urine of PCa patients and we identified one methylated site (cg05163709) as a potential biomarker. We evaluated the predictive capacity of the aberrant methylated sites using the area under receiver operating characteristic (ROC) curve (AUC). The ROC analysis showed a higher AUC for cg05163709 (0.915) than prostate-specific antigen (PSA, 0.769). These results indicated that aberrant DNA methylation of cg05163709 on the Y-chromosome could serve as a potential diagnostic biomarker with high sensitivity and specificity.
引用
收藏
页码:40611 / 40621
页数:11
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