SCT Promoter Methylation Is a Highly Discriminative Biomarker for Lung and Many Other Cancers

Adwait Sathe;Yu-An Zhang;Xiaotu Ma;Pradipta Ray;Daniela Cadinu;Yi-Wei Wang;Xiao Yao;Xiaoyun Liu;Hao Tang;Yunfei Wang;Ying Huang;Changning Liu;Jin Gu;Martin Akerman;Yifan Mo;Chao Cheng;Zhenyu Xuan;Lei Chen;Guanghua Xiao;Yang Xie;Luc Girard;Hongyang Wang;Stephen Lam;Ignacio I. Wistuba;Li Zhang;Adi F. Gazdar;Michael Q. Zhang
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Abstract

Aberrant DNA methylation has long been implicated in cancers. In this letter, we present a highly discriminative DNA methylation biomarker for non-small cell lung cancers (NSCLCs) and 14 other cancers. Based on 69 NSCLC cell lines and 257 cancer-free lung tissues, we identified a CpG island in SCT gene promoter, which was verified by qMSP experiment in 15 NSCLC cell lines and three immortalized human respiratory epithelium cells. In addition, we found that the SCT promoter was methylated in 23 cancer cell lines involving >10 cancer types profiled by ENCODE. We found that the SCT promoter is hypermethylated in primary tumors from TCGA lung cancer cohort. In addition, we found that SCT promoter is methylated at high frequencies in 15 malignancies and is not methylated in ~1000 non-cancerous tissues across >30 organ types. This letter indicates that SCT promoter methylation is a highly discriminative biomarker for lung and many other cancers.

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SCT启动子甲基化是肺癌和许多其他癌症的高度鉴别的生物标志物
长期以来,异常的DNA甲基化一直与癌症有关。在这封信中,我们提出了一种高度鉴别非小细胞肺癌(nsclc)和其他14种癌症的DNA甲基化生物标志物。基于69株非小细胞肺癌细胞株和257例无癌肺组织,我们在SCT基因启动子中发现了一个CpG岛,并在15株非小细胞肺癌细胞株和3个永生化人呼吸上皮细胞中进行了qMSP实验验证。此外,我们发现SCT启动子在23个癌细胞系中被甲基化,涉及bb1010种由ENCODE分析的癌症类型。我们发现SCT启动子在来自TCGA肺癌队列的原发肿瘤中是高甲基化的。此外,我们发现SCT启动子在15种恶性肿瘤中高频率甲基化,而在30种器官类型的约1000种非癌组织中不甲基化。这封信表明SCT启动子甲基化是肺癌和许多其他癌症的高度鉴别的生物标志物。
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