Validation ofSCTMethylation as a Hallmark Biomarker for Lung Cancers. Issue 3 (March 2016)

• Record Type: Journal Article
• Authors: Zhang, Yu‐An; Ma, Xiaotu; Sathe, Adwait; Fujimoto, Junya; Wistuba, Ignacio I.; Lam, Stephen; Yatabe, Yasushi; Wang, Yi‐Wei; Stastny, Victor; Gao, Boning; Larsen, Jill E.; Girard, Luc; Liu, Xiaoyun; Song, Kai; Behrens, Carmen; Kalhor, Neda; Xie, Yang; Zhang, Michael Q.; Minna, John D.; Gazdar, Adi F.
• Is Part Of: Journal of thoracic oncology. Volume 11:Issue 3(2016)
• Publication Date: 2016-03
• Subjects: SCT methylation -- Cancer biomarker -- Lung cancer -- FFPE DNA SCT qMSP -- Secretin; Chest -- Cancer -- Periodicals; Thoracic Neoplasms -- Periodicals; 616.99494005
• DOI: 10.1016/j.jtho.2015.11.004
• Languages: English
• ISSNs: 1556-0864

Abstract

ABSTRACT : Introduction: : The human secretin gene ( SCT ) encodes secretin, a hormone with limited tissue distribution. Analysis of the 450k methylation array data in The Cancer Genome Atlas (TCGA) indicated that the SCT promoter region is differentially hypermethylated in lung cancer. Our purpose was to validate SCT methylation as a potential biomarker for lung cancer. Methods: : We analyzed data from TCGA and developed and applied SCT ‐specific bisulfite DNA sequencing and quantitative methylation‐specific polymerase chain reaction assays. Results: : The analyses of TCGA 450K data for 801 samples showed that SCT hypermethylation has an area under the curve (AUC) value greater than 0.98 that can be used to distinguish lung adenocarcinomas or squamous cell carcinomas from nonmalignant lung tissue. Bisulfite sequencing of lung cancer cell lines and normal blood cells allowed us to confirm that SCT methylation is highly discriminative. By applying a quantitative methylation‐specific polymerase chain reaction assay, we found that SCT hypermethylation is frequently detected in all major subtypes of malignant non–small cell lung cancer (AUC = 0.92, n = 108) and small cell lung cancer (AUC = 0.93, n = 40) but is less frequent in lung carcinoids (AUC = 0.54, n = 20). SCT hypermethylation appeared in samples of lung carcinoma in situ during multistage pathogenesis and increased in invasive samples. Further analyses of TCGA 450k data showed that SCT hypermethylation is highly discriminative in most other types of malignant tumors but less frequent in low‐grade malignant tumors. The only normal tissue with a high level of methylation was the placenta. Conclusions: : Our findings demonstrated that SCT methylation is a highly discriminative biomarker for lung and other malignant tumors, is less frequent in low‐grade malignant tumors (including lung carcinoids), and appears at the carcinoma in situ stage.