Functional PIN1 promoter polymorphisms associated with risk of nasopharyngeal carcinoma in Southern Chinese populations

Abstract Our previous work reported the association between two single nucleotide polymorphisms (SNPs) in PIN1 promoter and nasopharyngeal carcinoma (NPC) risk with a small sample size in a low incidence area. This study investigated the association between the two SNPs and NPC risk in 733 patients...

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Autores principales: Liuyan Zeng, Shengqun Luo, Xin Li, Mengxuan Lu, Huahui Li, Tong Li, Guanhua Wang, Xiaoming Lyu, Wenrui Jia, Zigang Dong, Qiang Jiang, Zhihua Shen, Guo-Liang Huang, Zhiwei He
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Publicado: Nature Portfolio 2017
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spelling oai:doaj.org-article:c48bde0a6ecb44149fd93cfe2716c4e62021-12-02T15:05:49ZFunctional PIN1 promoter polymorphisms associated with risk of nasopharyngeal carcinoma in Southern Chinese populations10.1038/s41598-017-04156-z2045-2322https://doaj.org/article/c48bde0a6ecb44149fd93cfe2716c4e62017-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-04156-zhttps://doaj.org/toc/2045-2322Abstract Our previous work reported the association between two single nucleotide polymorphisms (SNPs) in PIN1 promoter and nasopharyngeal carcinoma (NPC) risk with a small sample size in a low incidence area. This study investigated the association between the two SNPs and NPC risk in 733 patients and 895 controls from a high incidence area. The results indicated the genotype and allele frequencies of -842G > C and -667C > T were both significantly different between patients and controls even using the resampling statistics. The -842GC and -667TT genotypes showed a significantly increased risk of NPC (OR = 1.977, 95% CI = 1.339–2.919, P = 0.001 and OR = 1.438, 95% CI = 1.061–1.922, P = 0.019, respectively). Compared to the most common -842G-667C haplotype, -842G-667T haplotype and -842C-667C haplotype showed a significantly increased risk of NPC (OR = 1.215, 95% CI = 1.053–1.402, P = 0.008 and OR = 2.268, 95% CI = 1.530–3.362, P = 0.001, respectively). Further reporter gene expression suggested that variant -842C-667C and -842G-667T were associated with an enhanced transcriptional activity. In conclusion, our findings suggest that -842G > C and -667C > T in PIN1 promoter are associated with NPC risk; as well as the promoter activity is mediated by functional PIN1 variants.Liuyan ZengShengqun LuoXin LiMengxuan LuHuahui LiTong LiGuanhua WangXiaoming LyuWenrui JiaZigang DongQiang JiangZhihua ShenGuo-Liang HuangZhiwei HeNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Liuyan Zeng
Shengqun Luo
Xin Li
Mengxuan Lu
Huahui Li
Tong Li
Guanhua Wang
Xiaoming Lyu
Wenrui Jia
Zigang Dong
Qiang Jiang
Zhihua Shen
Guo-Liang Huang
Zhiwei He
Functional PIN1 promoter polymorphisms associated with risk of nasopharyngeal carcinoma in Southern Chinese populations
description Abstract Our previous work reported the association between two single nucleotide polymorphisms (SNPs) in PIN1 promoter and nasopharyngeal carcinoma (NPC) risk with a small sample size in a low incidence area. This study investigated the association between the two SNPs and NPC risk in 733 patients and 895 controls from a high incidence area. The results indicated the genotype and allele frequencies of -842G > C and -667C > T were both significantly different between patients and controls even using the resampling statistics. The -842GC and -667TT genotypes showed a significantly increased risk of NPC (OR = 1.977, 95% CI = 1.339–2.919, P = 0.001 and OR = 1.438, 95% CI = 1.061–1.922, P = 0.019, respectively). Compared to the most common -842G-667C haplotype, -842G-667T haplotype and -842C-667C haplotype showed a significantly increased risk of NPC (OR = 1.215, 95% CI = 1.053–1.402, P = 0.008 and OR = 2.268, 95% CI = 1.530–3.362, P = 0.001, respectively). Further reporter gene expression suggested that variant -842C-667C and -842G-667T were associated with an enhanced transcriptional activity. In conclusion, our findings suggest that -842G > C and -667C > T in PIN1 promoter are associated with NPC risk; as well as the promoter activity is mediated by functional PIN1 variants.
format article
author Liuyan Zeng
Shengqun Luo
Xin Li
Mengxuan Lu
Huahui Li
Tong Li
Guanhua Wang
Xiaoming Lyu
Wenrui Jia
Zigang Dong
Qiang Jiang
Zhihua Shen
Guo-Liang Huang
Zhiwei He
author_facet Liuyan Zeng
Shengqun Luo
Xin Li
Mengxuan Lu
Huahui Li
Tong Li
Guanhua Wang
Xiaoming Lyu
Wenrui Jia
Zigang Dong
Qiang Jiang
Zhihua Shen
Guo-Liang Huang
Zhiwei He
author_sort Liuyan Zeng
title Functional PIN1 promoter polymorphisms associated with risk of nasopharyngeal carcinoma in Southern Chinese populations
title_short Functional PIN1 promoter polymorphisms associated with risk of nasopharyngeal carcinoma in Southern Chinese populations
title_full Functional PIN1 promoter polymorphisms associated with risk of nasopharyngeal carcinoma in Southern Chinese populations
title_fullStr Functional PIN1 promoter polymorphisms associated with risk of nasopharyngeal carcinoma in Southern Chinese populations
title_full_unstemmed Functional PIN1 promoter polymorphisms associated with risk of nasopharyngeal carcinoma in Southern Chinese populations
title_sort functional pin1 promoter polymorphisms associated with risk of nasopharyngeal carcinoma in southern chinese populations
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/c48bde0a6ecb44149fd93cfe2716c4e6
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