A panel of DNA methylation biomarkers for detection and improving diagnostic efficiency of lung cancer

Abstract Lung cancer remains the leading cause of cancer deaths worldwide. Although low-dose spiral computed tomography (LDCT) screening is used for the detection of lung cancer in a high-risk population, false-positive results of LDCT remain a clinical problem. Here, we developed a blood test of a...

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Main Authors: Bing Wei, Fengxin Wu, Wenqun Xing, Haibo Sun, Chi Yan, Chengzhi Zhao, Dongqing Wang, Xiaobing Chen, Yanli Chen, Mingming Li, Jie Ma
Format: Article
Language:English
Published: Nature Publishing Group 2021-08-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-96242-6
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spelling doaj-8541ccf271504b21b2b6ac9441c1c0c92021-08-22T11:27:01ZengNature Publishing GroupScientific Reports2045-23222021-08-0111111010.1038/s41598-021-96242-6A panel of DNA methylation biomarkers for detection and improving diagnostic efficiency of lung cancerBing Wei0Fengxin Wu1Wenqun Xing2Haibo Sun3Chi Yan4Chengzhi Zhao5Dongqing Wang6Xiaobing Chen7Yanli Chen8Mingming Li9Jie Ma10Department of Molecular Pathology, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer HospitalExcellen Medical Technology Co., Ltd.Department of Thoracic Surgery, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer HospitalDepartment of Thoracic Surgery, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer HospitalDepartment of Molecular Pathology, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer HospitalDepartment of Molecular Pathology, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer HospitalDepartment of Molecular Pathology, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer HospitalDepartment of Thoracic Surgery, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer HospitalExcellen Medical Technology Co., Ltd.Excellen Medical Technology Co., Ltd.Department of Molecular Pathology, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer HospitalAbstract Lung cancer remains the leading cause of cancer deaths worldwide. Although low-dose spiral computed tomography (LDCT) screening is used for the detection of lung cancer in a high-risk population, false-positive results of LDCT remain a clinical problem. Here, we developed a blood test of a novel panel of three established lung cancer methylation biomarkers for lung cancer detection. Short stature homeobox 2 gene (SHOX2), ras association domain family 1A gene (RASSF1A), and prostaglandin E receptor 4 gene (PTGER4) methylation was analyzed in a training cohort of 351 individuals (197 controls, 154 cases) and validated from an independent cohort of 149 subjects (89 controls, 60 cases). The novel panel biomarkers distinguished between malignant and benign lung disease at high sensitivity and specificity: 87.0% sensitivity [95% CI 80.2–91.5%], 98.0% specificity [95% CI 94.9–99.4%]. Sensitivity in adenocarcinoma, squamous cell carcinoma, small cell lung cancer, and other lung cancer was 89.0%, 87.5%, 85.7%, and 77.8%, respectively. Notably, cancer patients in stage I and II showed high diagnostic sensitivity at 82.5% and 90.5%, respectively. Moreover, the diagnostic efficiency did not show bias toward age, gender, smoking, and the presence of other (nonlung) cancers. The performance of the panel in the validation cohort confirmed the diagnostic value. These findings clearly showed that this panel of DNA methylation biomarkers was effective in detecting lung cancer noninvasively and may provide clinical utility in stand-alone or in combination with current imaging techniques to improve the diagnosis of lung cancer.https://doi.org/10.1038/s41598-021-96242-6
collection DOAJ
language English
format Article
sources DOAJ
author Bing Wei
Fengxin Wu
Wenqun Xing
Haibo Sun
Chi Yan
Chengzhi Zhao
Dongqing Wang
Xiaobing Chen
Yanli Chen
Mingming Li
Jie Ma
spellingShingle Bing Wei
Fengxin Wu
Wenqun Xing
Haibo Sun
Chi Yan
Chengzhi Zhao
Dongqing Wang
Xiaobing Chen
Yanli Chen
Mingming Li
Jie Ma
A panel of DNA methylation biomarkers for detection and improving diagnostic efficiency of lung cancer
Scientific Reports
author_facet Bing Wei
Fengxin Wu
Wenqun Xing
Haibo Sun
Chi Yan
Chengzhi Zhao
Dongqing Wang
Xiaobing Chen
Yanli Chen
Mingming Li
Jie Ma
author_sort Bing Wei
title A panel of DNA methylation biomarkers for detection and improving diagnostic efficiency of lung cancer
title_short A panel of DNA methylation biomarkers for detection and improving diagnostic efficiency of lung cancer
title_full A panel of DNA methylation biomarkers for detection and improving diagnostic efficiency of lung cancer
title_fullStr A panel of DNA methylation biomarkers for detection and improving diagnostic efficiency of lung cancer
title_full_unstemmed A panel of DNA methylation biomarkers for detection and improving diagnostic efficiency of lung cancer
title_sort panel of dna methylation biomarkers for detection and improving diagnostic efficiency of lung cancer
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-08-01
description Abstract Lung cancer remains the leading cause of cancer deaths worldwide. Although low-dose spiral computed tomography (LDCT) screening is used for the detection of lung cancer in a high-risk population, false-positive results of LDCT remain a clinical problem. Here, we developed a blood test of a novel panel of three established lung cancer methylation biomarkers for lung cancer detection. Short stature homeobox 2 gene (SHOX2), ras association domain family 1A gene (RASSF1A), and prostaglandin E receptor 4 gene (PTGER4) methylation was analyzed in a training cohort of 351 individuals (197 controls, 154 cases) and validated from an independent cohort of 149 subjects (89 controls, 60 cases). The novel panel biomarkers distinguished between malignant and benign lung disease at high sensitivity and specificity: 87.0% sensitivity [95% CI 80.2–91.5%], 98.0% specificity [95% CI 94.9–99.4%]. Sensitivity in adenocarcinoma, squamous cell carcinoma, small cell lung cancer, and other lung cancer was 89.0%, 87.5%, 85.7%, and 77.8%, respectively. Notably, cancer patients in stage I and II showed high diagnostic sensitivity at 82.5% and 90.5%, respectively. Moreover, the diagnostic efficiency did not show bias toward age, gender, smoking, and the presence of other (nonlung) cancers. The performance of the panel in the validation cohort confirmed the diagnostic value. These findings clearly showed that this panel of DNA methylation biomarkers was effective in detecting lung cancer noninvasively and may provide clinical utility in stand-alone or in combination with current imaging techniques to improve the diagnosis of lung cancer.
url https://doi.org/10.1038/s41598-021-96242-6
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