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Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA).

Authors :
Hosgood HD 3rd
Song M
Hsiung CA
Yin Z
Shu XO
Wang Z
Chatterjee N
Zheng W
Caporaso N
Burdette L
Yeager M
Berndt SI
Landi MT
Chen CJ
Chang GC
Hsiao CF
Tsai YH
Chien LH
Chen KY
Huang MS
Su WC
Chen YM
Chen CH
Yang TY
Wang CL
Hung JY
Lin CC
Perng RP
Chen CY
Chen KC
Li YJ
Yu CJ
Chen YS
Chen YH
Tsai FY
Kim C
Seow WJ
Bassig BA
Wu W
Guan P
He Q
Gao YT
Cai Q
Chow WH
Xiang YB
Lin D
Wu C
Wu YL
Shin MH
Hong YC
Matsuo K
Chen K
Wong MP
Lu D
Jin L
Wang JC
Seow A
Wu T
Shen H
Fraumeni JF Jr
Yang PC
Chang IS
Zhou B
Chanock SJ
Rothman N
Lan Q
Source :
Human genetics [Hum Genet] 2015 Mar; Vol. 134 (3), pp. 333-41. Date of Electronic Publication: 2015 Jan 08.
Publication Year :
2015

Abstract

We previously carried out a multi-stage genome-wide association study (GWAS) on lung cancer among never smokers in the Female Lung Cancer Consortium in Asia (FLCCA) (6,609 cases, 7,457 controls) that identified novel susceptibility loci at 10q25.2, 6q22.2, and 6p21.32, and confirmed two previously identified loci at 5p15.33 and 3q28. Household air pollution (HAP) attributed to solid fuel burning for heating and cooking, is the leading cause of the overall disease burden in Southeast Asia, and is known to contain lung carcinogens. To evaluate the gene-HAP interactions associated with lung cancer in loci independent of smoking, we analyzed data from studies participating in FLCCA with fuel use information available (n = 3; 1,731 cases; 1,349 controls). Coal use was associated with a 30% increased risk of lung cancer (OR 1.3, 95% CI 1.0-1.6). Among the five a priori SNPs identified by our GWAS, two showed a significant interaction with coal use (HLA Class II rs2395185, p = 0.02; TP63 rs4488809 (rs4600802), p = 0.04). The risk of lung cancer associated with coal exposure varied with the respective alleles for these two SNPs. Our observations provide evidence that genetic variation in HLA Class II and TP63 may modify the association between HAP and lung cancer risk. The roles played in the cell cycle and inflammation pathways by the proteins encoded by these two genes provide biological plausibility for these interactions; however, additional replication studies are needed in other non-smoking populations.

Details

Language :
English
ISSN :
1432-1203
Volume :
134
Issue :
3
Database :
MEDLINE
Journal :
Human genetics
Publication Type :
Academic Journal
Accession number :
25566987
Full Text :
https://doi.org/10.1007/s00439-014-1528-z