Integrative Genomics of Emphysema-Associated Genes Reveals Potential Disease Biomarkers

被引:26
|
作者
Obeidat, Ma'en [1 ]
Nie, Yunlong [1 ]
Fishbane, Nick [1 ]
Li, Xuan [1 ]
Bosse, Yohan [2 ,3 ]
Joubert, Philippe [3 ,4 ]
Nickle, David C. [5 ]
Hao, Ke [6 ]
Postma, Dirkje S. [7 ]
Timens, Wim [8 ]
Sze, Marc A. [1 ]
Shannon, Casey P. [9 ]
Hollander, Zsuzsanna [9 ]
Ng, Raymond T. [9 ]
McManus, Bruce [1 ,9 ]
Miller, Bruce E. [10 ]
Rennard, Stephen [11 ,12 ]
Spira, Avrum [13 ]
Hackett, Tillie-Louise [1 ,14 ]
Lam, Wan [15 ]
Lam, Stephen [15 ]
Faner, Rosa [16 ]
Agusti, Alvar [16 ]
Hogg, James C. [1 ,17 ]
Sin, Don D. [1 ,18 ]
Pare, Peter D. [1 ,18 ]
机构
[1] Univ British Columbia, St Pauls Hosp, Ctr Heart Lung Innovat, Room 166,1081 Burrard St, Vancouver, BC V6Z 1Y6, Canada
[2] Laval Univ, Dept Mol Med, Quebec City, PQ, Canada
[3] Laval Univ, Inst Univ Cardiol & Pneumol Quebec, Quebec City, PQ, Canada
[4] Laval Univ, Dept Mol Biol Med Biochem & Pathol, Quebec City, PQ, Canada
[5] Merck Res Labs, Genet & Pharmacogen, Boston, MA USA
[6] Icahn Sch Med Mt Sinai, Icahn Inst Genom & Multiscale Biol, New York, NY 10029 USA
[7] Univ Groningen, Univ Med Ctr Groningen, GRIAC Res Inst, Dept Pulmonol, Groningen, Netherlands
[8] Univ Groningen, Univ Med Ctr Groningen, GRIAC Res Inst, Dept Pathol & Med Biol, Groningen, Netherlands
[9] Prevent Organ Failure PROOF Ctr Excellence, Vancouver, BC, Canada
[10] GlaxoSmithKline, King Of Prussia, PA USA
[11] Univ Nebraska Med Ctr, Div Pulm & Crit Care Med, Omaha, NE USA
[12] AstraZeneca, Clin Discovery Unit, Early Clin Dev, Cambridge, England
[13] Boston Univ, Sch Med, Dept Med, Div Computat Biomed, Boston, MA 02118 USA
[14] Univ British Columbia, Dept Anesthesiol Pharmacol & Therapeut, Vancouver, BC, Canada
[15] British Columbia Canc Res Ctr, Dept Integrat Oncol, Vancouver, BC, Canada
[16] Fundacio Clin Recerca Biomed, Barcelona, Spain
[17] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC, Canada
[18] Univ British Columbia, Resp Div, Dept Med, Vancouver, BC, Canada
基金
中国国家自然科学基金;
关键词
blood; FEV1; lung; mRNA; biomarker; OBSTRUCTIVE PULMONARY-DISEASE; LUNG-FUNCTION; SIGNATURE; TISSUE;
D O I
10.1165/rcmb.2016-0284OC
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chronic obstructive pulmonary disease is the third leading cause of death worldwide. Gene expression profiling across multiple regions of the same lung identified genes significantly related to emphysema. We sought to determine whether the lung and epithelial expression of 127 emphysema-related genes was also related to lung function in independent cohorts, and whether any of these genes could be used as biomarkers in the peripheral blood of patients with chronic obstructive pulmonary disease. To that end, we examined whether the expression levels of these genes were under genetic control inlung tissue (n = 1,111). We then determined whether the mRNA levels of these genes in lung tissue (n = 727), small airway epithelial cells (n = 238), and peripheral blood (n = 620) were significantly related to lung functionmeasurements. The expression of 63 of the 127 genes (50%) was under genetic control in lung tissue. The lung and epithelial mRNA expression of a subset of the emphysema-associated genes, including ASRGL1, LPHN2, and EDNRB, was strongly associated with lung function. In peripheral blood, the expression of 40 genes was significantly associated with lung function. Twenty-nine of these genes (73%) were also associated with lung function in lung tissue, but with the opposite direction of effect for 24 of the 29 genes, including those involved in hypoxia and B cell-related responses. The integrative genomics approach uncovered a significant overlap of emphysema genes associations with lung function between lung and blood with opposite directions between the two. These results support the use of peripheral blood to detect disease biomarkers.
引用
收藏
页码:411 / 418
页数:8
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