author_facet Hu, Zhibin
Ma, Hongxia
Lu, Daru
Qian, Ji
Zhou, Jiannong
Chen, Yijiang
Xu, Lin
Wang, Xinru
Wei, Qingyi
Shen, Hongbing
Hu, Zhibin
Ma, Hongxia
Lu, Daru
Qian, Ji
Zhou, Jiannong
Chen, Yijiang
Xu, Lin
Wang, Xinru
Wei, Qingyi
Shen, Hongbing
author Hu, Zhibin
Ma, Hongxia
Lu, Daru
Qian, Ji
Zhou, Jiannong
Chen, Yijiang
Xu, Lin
Wang, Xinru
Wei, Qingyi
Shen, Hongbing
spellingShingle Hu, Zhibin
Ma, Hongxia
Lu, Daru
Qian, Ji
Zhou, Jiannong
Chen, Yijiang
Xu, Lin
Wang, Xinru
Wei, Qingyi
Shen, Hongbing
International Journal of Cancer
Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
Cancer Research
Oncology
author_sort hu, zhibin
spelling Hu, Zhibin Ma, Hongxia Lu, Daru Qian, Ji Zhou, Jiannong Chen, Yijiang Xu, Lin Wang, Xinru Wei, Qingyi Shen, Hongbing 0020-7136 1097-0215 Wiley Cancer Research Oncology http://dx.doi.org/10.1002/ijc.21463 <jats:title>Abstract</jats:title><jats:p>Overexpression of MDM2 may attenuate the P53 stress response pathway through direct blocking of P53 transcriptional activity and mediating P53 degradation. Two promoter polymorphisms (one is a T to G substitution at the intronic P53‐response promoter, and the other is a 40‐bp insertion/deletion polymorphism in the constitutive promoter) were identified, and recently the T/G substitution (SNP309) has been demonstrated to alter the levels of <jats:italic>MDM2</jats:italic> gene products. In this molecular epidemiological study with 717 incident lung cancer cases and 1,083 cancer‐free controls, we genotyped these 2 promoter polymorphisms of <jats:italic>MDM2</jats:italic> and evaluated their associations with risk of lung cancer. We found that there were no significant associations between <jats:italic>MDM2</jats:italic> SNP309 variant genotypes and lung cancer risk (adjusted OR = 1.20, 95% CI = 0.95–1.53 for TG and adjusted OR = 1.12, 95% CI = 0.85–1.48 for GG, respectively). Similarly, we did not find evidence for any association between risk of lung cancer and <jats:italic>MDM2</jats:italic> insertion/deletion polymorphism. The findings suggest that these two <jats:italic>MDM2</jats:italic> promoter polymorphisms may not play a major role in lung cancer susceptibility in this Chinese population. © 2005 Wiley‐Liss, Inc.</jats:p> Genetic variants in the <i>MDM2</i> promoter and lung cancer risk in a Chinese population International Journal of Cancer
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title Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
title_unstemmed Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
title_full Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
title_fullStr Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
title_full_unstemmed Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
title_short Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
title_sort genetic variants in the <i>mdm2</i> promoter and lung cancer risk in a chinese population
topic Cancer Research
Oncology
url http://dx.doi.org/10.1002/ijc.21463
publishDate 2006
physical 1275-1278
description <jats:title>Abstract</jats:title><jats:p>Overexpression of MDM2 may attenuate the P53 stress response pathway through direct blocking of P53 transcriptional activity and mediating P53 degradation. Two promoter polymorphisms (one is a T to G substitution at the intronic P53‐response promoter, and the other is a 40‐bp insertion/deletion polymorphism in the constitutive promoter) were identified, and recently the T/G substitution (SNP309) has been demonstrated to alter the levels of <jats:italic>MDM2</jats:italic> gene products. In this molecular epidemiological study with 717 incident lung cancer cases and 1,083 cancer‐free controls, we genotyped these 2 promoter polymorphisms of <jats:italic>MDM2</jats:italic> and evaluated their associations with risk of lung cancer. We found that there were no significant associations between <jats:italic>MDM2</jats:italic> SNP309 variant genotypes and lung cancer risk (adjusted OR = 1.20, 95% CI = 0.95–1.53 for TG and adjusted OR = 1.12, 95% CI = 0.85–1.48 for GG, respectively). Similarly, we did not find evidence for any association between risk of lung cancer and <jats:italic>MDM2</jats:italic> insertion/deletion polymorphism. The findings suggest that these two <jats:italic>MDM2</jats:italic> promoter polymorphisms may not play a major role in lung cancer susceptibility in this Chinese population. © 2005 Wiley‐Liss, Inc.</jats:p>
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author Hu, Zhibin, Ma, Hongxia, Lu, Daru, Qian, Ji, Zhou, Jiannong, Chen, Yijiang, Xu, Lin, Wang, Xinru, Wei, Qingyi, Shen, Hongbing
author_facet Hu, Zhibin, Ma, Hongxia, Lu, Daru, Qian, Ji, Zhou, Jiannong, Chen, Yijiang, Xu, Lin, Wang, Xinru, Wei, Qingyi, Shen, Hongbing, Hu, Zhibin, Ma, Hongxia, Lu, Daru, Qian, Ji, Zhou, Jiannong, Chen, Yijiang, Xu, Lin, Wang, Xinru, Wei, Qingyi, Shen, Hongbing
author_sort hu, zhibin
container_issue 5
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container_title International Journal of Cancer
container_volume 118
description <jats:title>Abstract</jats:title><jats:p>Overexpression of MDM2 may attenuate the P53 stress response pathway through direct blocking of P53 transcriptional activity and mediating P53 degradation. Two promoter polymorphisms (one is a T to G substitution at the intronic P53‐response promoter, and the other is a 40‐bp insertion/deletion polymorphism in the constitutive promoter) were identified, and recently the T/G substitution (SNP309) has been demonstrated to alter the levels of <jats:italic>MDM2</jats:italic> gene products. In this molecular epidemiological study with 717 incident lung cancer cases and 1,083 cancer‐free controls, we genotyped these 2 promoter polymorphisms of <jats:italic>MDM2</jats:italic> and evaluated their associations with risk of lung cancer. We found that there were no significant associations between <jats:italic>MDM2</jats:italic> SNP309 variant genotypes and lung cancer risk (adjusted OR = 1.20, 95% CI = 0.95–1.53 for TG and adjusted OR = 1.12, 95% CI = 0.85–1.48 for GG, respectively). Similarly, we did not find evidence for any association between risk of lung cancer and <jats:italic>MDM2</jats:italic> insertion/deletion polymorphism. The findings suggest that these two <jats:italic>MDM2</jats:italic> promoter polymorphisms may not play a major role in lung cancer susceptibility in this Chinese population. © 2005 Wiley‐Liss, Inc.</jats:p>
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spelling Hu, Zhibin Ma, Hongxia Lu, Daru Qian, Ji Zhou, Jiannong Chen, Yijiang Xu, Lin Wang, Xinru Wei, Qingyi Shen, Hongbing 0020-7136 1097-0215 Wiley Cancer Research Oncology http://dx.doi.org/10.1002/ijc.21463 <jats:title>Abstract</jats:title><jats:p>Overexpression of MDM2 may attenuate the P53 stress response pathway through direct blocking of P53 transcriptional activity and mediating P53 degradation. Two promoter polymorphisms (one is a T to G substitution at the intronic P53‐response promoter, and the other is a 40‐bp insertion/deletion polymorphism in the constitutive promoter) were identified, and recently the T/G substitution (SNP309) has been demonstrated to alter the levels of <jats:italic>MDM2</jats:italic> gene products. In this molecular epidemiological study with 717 incident lung cancer cases and 1,083 cancer‐free controls, we genotyped these 2 promoter polymorphisms of <jats:italic>MDM2</jats:italic> and evaluated their associations with risk of lung cancer. We found that there were no significant associations between <jats:italic>MDM2</jats:italic> SNP309 variant genotypes and lung cancer risk (adjusted OR = 1.20, 95% CI = 0.95–1.53 for TG and adjusted OR = 1.12, 95% CI = 0.85–1.48 for GG, respectively). Similarly, we did not find evidence for any association between risk of lung cancer and <jats:italic>MDM2</jats:italic> insertion/deletion polymorphism. The findings suggest that these two <jats:italic>MDM2</jats:italic> promoter polymorphisms may not play a major role in lung cancer susceptibility in this Chinese population. © 2005 Wiley‐Liss, Inc.</jats:p> Genetic variants in the <i>MDM2</i> promoter and lung cancer risk in a Chinese population International Journal of Cancer
spellingShingle Hu, Zhibin, Ma, Hongxia, Lu, Daru, Qian, Ji, Zhou, Jiannong, Chen, Yijiang, Xu, Lin, Wang, Xinru, Wei, Qingyi, Shen, Hongbing, International Journal of Cancer, Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population, Cancer Research, Oncology
title Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
title_full Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
title_fullStr Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
title_full_unstemmed Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
title_short Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
title_sort genetic variants in the <i>mdm2</i> promoter and lung cancer risk in a chinese population
title_unstemmed Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population
topic Cancer Research, Oncology
url http://dx.doi.org/10.1002/ijc.21463