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The Overlap of Lung Tissue Transcriptome of Smoke Exposed Mice with Human Smoking and COPD.
Obeidat, Ma'en; Dvorkin-Gheva, Anna; Li, Xuan; Bossé, Yohan; Brandsma, Corry-Anke; Nickle, David C; Hansbro, Philip M; Faner, Rosa; Agusti, Alvar; Paré, Peter D; Stampfli, Martin R; Sin, Don D.
Affiliation
  • Obeidat M; The University of British Columbia Center for Heart Lung Innovation, St Paul's Hospital, Vancouver, Canada.
  • Dvorkin-Gheva A; Department of Pathology and Molecular Medicine, McMaster Immunology Research Centre, Hamilton, ON, Canada.
  • Li X; The University of British Columbia Center for Heart Lung Innovation, St Paul's Hospital, Vancouver, Canada.
  • Bossé Y; Institut universitaire de cardiologie et de pneumologie de Québec, Québec, Canada.
  • Brandsma CA; Department of Molecular Medicine, Laval University, Québec, Canada.
  • Nickle DC; University of Groningen, University Medical Center Groningen, Department of Pathology and Medical Biology, Groningen, The Netherlands.
  • Hansbro PM; Merck & Co., Inc., MRL, Kenilworth, New Jersey, United States of America.
  • Faner R; Priority Research Centre for Healthy Lungs, University of Newcastle, Newcastle, New South Wales, Australia.
  • Agusti A; Hunter Medical Research Institute, Newcastle, New South Wales, Australia.
  • Paré PD; Fundacio Clinic per a la Recerca Biomedica Barcelona, Barcelona, Spain.
  • Stampfli MR; Fundacio Clinic per a la Recerca Biomedica Barcelona, Barcelona, Spain.
  • Sin DD; Respiratory Institute, Hospital Clinic, University of Barcelona, Institut d'investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Sci Rep ; 8(1): 11881, 2018 08 08.
Article in En | MEDLINE | ID: mdl-30089872
ABSTRACT
Genome-wide mRNA profiling in lung tissue from human and animal models can provide novel insights into the pathogenesis of chronic obstructive pulmonary disease (COPD). While 6 months of smoke exposure are widely used, shorter durations were also reported. The overlap of short term and long-term smoke exposure in mice is currently not well understood, and their representation of the human condition is uncertain. Lung tissue gene expression profiles of six murine smoking experiments (n = 48) were obtained from the Gene Expression Omnibus (GEO) and analyzed to identify the murine smoking signature. The "human smoking" gene signature containing 386 genes was previously published in the lung eQTL study (n = 1,111). A signature of mild COPD containing 7 genes was also identified in the same study. The lung tissue gene signature of "severe COPD" (n = 70) contained 4,071 genes and was previously published. We detected 3,723 differentially expressed genes in the 6 month-exposure mice datasets (FDR <0.1). Of those, 184 genes (representing 48% of human smoking) and 1,003 (representing 27% of human COPD) were shared with the human smoking-related genes and the COPD severity-related genes, respectively. There was 4-fold over-representation of human and murine smoking-related genes (P = 6.7 × 10-26) and a 1.4 fold in the severe COPD -related genes (P = 2.3 × 10-12). There was no significant enrichment of the mice and human smoking-related genes in mild COPD signature. These data suggest that murine smoke models are strongly representative of molecular processes of human smoking but less of COPD.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Smoke / Smoking / Pulmonary Disease, Chronic Obstructive / Transcriptome / Lung Limits: Animals / Humans Language: En Journal: Sci Rep Year: 2018 Document type: Article Affiliation country: Canada

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Smoke / Smoking / Pulmonary Disease, Chronic Obstructive / Transcriptome / Lung Limits: Animals / Humans Language: En Journal: Sci Rep Year: 2018 Document type: Article Affiliation country: Canada