Identification of novel epigenetic abnormalities as sputum biomarkers for lung cancer risk among smokers and COPD patients
Autor: | Yong Lin, Scott H. Randell, Hans Petersen, Maria A. Picchi, Steven A. Belinsky, Yohannes Tesfaigzi, Mathewos Tessema, Dereje D. Tassew, Guodong Wu, Christin M. Yingling, Kieu Do |
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Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Pulmonary and Respiratory Medicine Oncology Cancer Research medicine.medical_specialty Lung Neoplasms Article Epigenesis Genetic Transcriptome Pulmonary Disease Chronic Obstructive 03 medical and health sciences 0302 clinical medicine Internal medicine medicine Humans Epigenetics Risk factor Lung cancer Lung COPD Smokers business.industry Sputum DNA Methylation medicine.disease respiratory tract diseases 030104 developmental biology medicine.anatomical_structure 030220 oncology & carcinogenesis Adenocarcinoma medicine.symptom business Biomarkers |
Zdroj: | Lung Cancer |
ISSN: | 0169-5002 |
DOI: | 10.1016/j.lungcan.2020.05.017 |
Popis: | Objectives Smoking is a common risk factor for chronic obstructive pulmonary disease (COPD) and lung cancer. Although COPD patients have higher risk of lung cancer compared to non-COPD smokers, the molecular links between these diseases are not well-defined. This study aims to identify genes that are downregulated by cigarette smoke and commonly repressed in COPD and lung cancer. Materials and methods Primary human airway epithelial cells (HAEC) were exposed to cigarette-smoke-extract (CSE) for 10-weeks and significantly suppressed genes were identified by transcriptome array. Epigenetic abnormalities of these genes in lung adenocarcinoma (LUAD) from patients with or without COPD were determined using genome-wide and gene-specific assays and by in vitro treatment of cell lines with trichostatin-A or 5-aza-2-deoxycytidine. Results The ten most commonly downregulated genes following chronic CSE exposure of HAEC and show promoter hypermethylation in LUAD were selected. Among these, expression of CCNA1, SNCA, and ZNF549 was significantly reduced in lung tissues from COPD compared with non-COPD cases while expression of CCNA1 and SNCA was further downregulated in tumors with COPD. The promoter regions of all three genes were hypermethylated in LUAD but not normal or COPD lungs. The reduced expression and aberrant promoter hypermethylation of these genes in LUAD were independently validated using data from the Cancer Genome Atlas project. Importantly, SNCA and ZNF549 methylation detected in sputum DNA from LUAD (52% and 38%) cases were more prevalent compared to cancer-free smokers (26% and 15%), respectively (p Conclusions Our data show that suppression of CCNA1, SNCA, and ZNF549 in lung cancer and COPD occurs with or without promoter hypermethylation, respectively. Detecting methylation of these and previously identified genes in sputum of cancer-free smokers may serve as non-invasive biomarkers for early detection of lung cancer among high risk smokers including COPD patients. |
Databáze: | OpenAIRE |
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