TY - JOUR
T1 - Association of CYP19A1 polymorphisms with risks for atypical adenomatous hyperplasia and bronchioloalveolar carcinoma in the lungs
AU - Kohno, Takashi
AU - Kakinuma, Ryutaro
AU - Iwasaki, Motoki
AU - Yamaji, Taiki
AU - Kunitoh, Hideo
AU - Suzuki, Kenji
AU - Shimada, Yoko
AU - Shiraishi, Kouya
AU - Kasuga, Yoshio
AU - Hamada, Gerson Shigeaki
AU - Furuta, Koh
AU - Tsuta, Koji
AU - Sakamoto, Hiromi
AU - Kuchiba, Aya
AU - Yamamoto, Seiichiro
AU - Kanai, Yae
AU - Tsugane, Shoichiro
AU - Yokota, Jun
N1 - Funding Information:
Grants-in-Aid from the Ministry of Health, Labor and Welfare for the Third-term Comprehensive 10 year Strategy for Cancer Control, Cancer Research (19S-1), Research on Risk of Chemical Substances; Ministry of Education, Culture, Sports, Science and Technology for Scientific Research on Priority Areas (20014031 and 17015049); Program for Promotion of Fundamental Studies in Health Sciences of the National Institute of Biomedical Innovation.
PY - 2010/8/5
Y1 - 2010/8/5
N2 - Estrogen has been indicated to play an etiological role in the development of lung adenocarcinoma (ADC), particularly bronchioloalveolar carcinoma (BAC), a type of ADC that develops from a benign adenomatous lesion, atypical adenomatous hyperplasia (AAH). Polymorphisms in the CYP19A1 gene cause interindividual differences in estrogen levels. Here, 13 CYP19A1 singlenucleotide polymorphisms (SNPs) were examined for associations with lung AAH risk. AAH is detected as ground-glass opacity (GGO) by computed tomography (CT) examination, and this study consisted of 100 individuals diagnosed with GGO in their lungs among 3088 CT-based cancer screening examinees and 424 without. Minor allele carriers for the rs3764221 SNP showed an elevated risk for GGO [odds ratio (OR) = 1.72, P = 0.017]. Associations of this SNP with risks for lung AAH and BAC in the lungs were next examined using 359 ADC cases whose resected lung lobes were subjected to a histological examination for AAH accompaniment and the presence of BAC components and 330 controls without cancer. The ORs were also increased for lung ADC accompanied by AAH (OR = 1.74, P = 0.029) as well as lung ADC with BAC components (OR = 1.41, P = 0.091). The minor allele was associated with an increased circulating estradiol level (P = 0.079) in a population of 363 postmenopausal women without cancer. These results indicate that CYP19A1 polymorphisms are involved in the risk for lung AAH and BAC in the lungs by causing differences in estrogen levels.
AB - Estrogen has been indicated to play an etiological role in the development of lung adenocarcinoma (ADC), particularly bronchioloalveolar carcinoma (BAC), a type of ADC that develops from a benign adenomatous lesion, atypical adenomatous hyperplasia (AAH). Polymorphisms in the CYP19A1 gene cause interindividual differences in estrogen levels. Here, 13 CYP19A1 singlenucleotide polymorphisms (SNPs) were examined for associations with lung AAH risk. AAH is detected as ground-glass opacity (GGO) by computed tomography (CT) examination, and this study consisted of 100 individuals diagnosed with GGO in their lungs among 3088 CT-based cancer screening examinees and 424 without. Minor allele carriers for the rs3764221 SNP showed an elevated risk for GGO [odds ratio (OR) = 1.72, P = 0.017]. Associations of this SNP with risks for lung AAH and BAC in the lungs were next examined using 359 ADC cases whose resected lung lobes were subjected to a histological examination for AAH accompaniment and the presence of BAC components and 330 controls without cancer. The ORs were also increased for lung ADC accompanied by AAH (OR = 1.74, P = 0.029) as well as lung ADC with BAC components (OR = 1.41, P = 0.091). The minor allele was associated with an increased circulating estradiol level (P = 0.079) in a population of 363 postmenopausal women without cancer. These results indicate that CYP19A1 polymorphisms are involved in the risk for lung AAH and BAC in the lungs by causing differences in estrogen levels.
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U2 - 10.1093/carcin/bgq159
DO - 10.1093/carcin/bgq159
M3 - Article
C2 - 20688833
AN - SCOPUS:77957813234
SN - 0143-3334
VL - 31
SP - 1794
EP - 1799
JO - Carcinogenesis
JF - Carcinogenesis
IS - 10
ER -