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The Leptin Gene Family and Colorectal Cancer: Interaction with Smoking Behavior and Family History of Cancer
BACKGROUND: Pathologic condition associated with metabolic syndrome traits seems to increase the risk of colorectal cancer. One mechanism underlying this relationship may involve the growth-promoting effects of the circulation hormones associated with obesity and insulin resistance, such as leptin....
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3620466/ https://www.ncbi.nlm.nih.gov/pubmed/23593308 http://dx.doi.org/10.1371/journal.pone.0060777 |
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author | Liu, Li Zhong, Rong Wei, Sheng Xiang, Hao Chen, Jigui Xie, Duoshuang Yin, Jieyun Zou, Li Sun, Jingwen Chen, Wei Miao, Xiaoping Nie, Shaofa |
author_facet | Liu, Li Zhong, Rong Wei, Sheng Xiang, Hao Chen, Jigui Xie, Duoshuang Yin, Jieyun Zou, Li Sun, Jingwen Chen, Wei Miao, Xiaoping Nie, Shaofa |
author_sort | Liu, Li |
collection | PubMed |
description | BACKGROUND: Pathologic condition associated with metabolic syndrome traits seems to increase the risk of colorectal cancer. One mechanism underlying this relationship may involve the growth-promoting effects of the circulation hormones associated with obesity and insulin resistance, such as leptin. METHODOLOGY/PRINCIPAL FINDINGS: A two-stage case-control study was used to explore the role of polymorphisms of Leptin (LEP) and Leptin receptor (LEPR), either alone or in combination with environmental factors in colorectal carcinogenesis. In stage 1, 20 single nucleotide polymorphisms (SNPs) that tag common SNPs in these two genes were genotyped among 470 cases and 458 controls. In stage 2, another population with 314 cases and 355 controls were genotyped for the two most promising SNPs from stage 1. LEPR rs12037879 only presented modestly increased colorectal cancer risk, with odds ratios of 1.41 (95% confidence interval [CI] 1.13–1.76) and 1.74 (95%CI 1.08–2.81) for GA and AA genotype when compared with GG genotype in combined population. Smokers carrying LEPR rs12037879 A allele presented 1.67-fold (95%CI 1.39-fold to 2.01-fold) increased colorectal cancer risk when compared with non-smokers carrying GG genotype in combined analysis. Individuals with family history of cancer harboring LEPR rs12037879 A allele showed 1.52-fold (95%CI: 1.24-fold to 1.86-fold) increased colorectal cancer risk, compared with individuals without family history of cancer harboring GG genotype. Multifactor gene-environment interaction analysis revealed significant interactions among LEPR rs12037879, LEPR rs6690625, smoking status and family history of cancer, exhibiting a gradient of increased colorectal cancer risk along with the increasing number of risk factors (P = 9.82×10(−10)). CONCLUSIONS/SIGNIFICANCE: Our research supports that polymorphisms in LEPR may be associated with marginal increase in the risk for colorectal cancer. Moreover, this association could be strengthened by cigarette smoking and family history of cancer. |
format | Online Article Text |
id | pubmed-3620466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36204662013-04-16 The Leptin Gene Family and Colorectal Cancer: Interaction with Smoking Behavior and Family History of Cancer Liu, Li Zhong, Rong Wei, Sheng Xiang, Hao Chen, Jigui Xie, Duoshuang Yin, Jieyun Zou, Li Sun, Jingwen Chen, Wei Miao, Xiaoping Nie, Shaofa PLoS One Research Article BACKGROUND: Pathologic condition associated with metabolic syndrome traits seems to increase the risk of colorectal cancer. One mechanism underlying this relationship may involve the growth-promoting effects of the circulation hormones associated with obesity and insulin resistance, such as leptin. METHODOLOGY/PRINCIPAL FINDINGS: A two-stage case-control study was used to explore the role of polymorphisms of Leptin (LEP) and Leptin receptor (LEPR), either alone or in combination with environmental factors in colorectal carcinogenesis. In stage 1, 20 single nucleotide polymorphisms (SNPs) that tag common SNPs in these two genes were genotyped among 470 cases and 458 controls. In stage 2, another population with 314 cases and 355 controls were genotyped for the two most promising SNPs from stage 1. LEPR rs12037879 only presented modestly increased colorectal cancer risk, with odds ratios of 1.41 (95% confidence interval [CI] 1.13–1.76) and 1.74 (95%CI 1.08–2.81) for GA and AA genotype when compared with GG genotype in combined population. Smokers carrying LEPR rs12037879 A allele presented 1.67-fold (95%CI 1.39-fold to 2.01-fold) increased colorectal cancer risk when compared with non-smokers carrying GG genotype in combined analysis. Individuals with family history of cancer harboring LEPR rs12037879 A allele showed 1.52-fold (95%CI: 1.24-fold to 1.86-fold) increased colorectal cancer risk, compared with individuals without family history of cancer harboring GG genotype. Multifactor gene-environment interaction analysis revealed significant interactions among LEPR rs12037879, LEPR rs6690625, smoking status and family history of cancer, exhibiting a gradient of increased colorectal cancer risk along with the increasing number of risk factors (P = 9.82×10(−10)). CONCLUSIONS/SIGNIFICANCE: Our research supports that polymorphisms in LEPR may be associated with marginal increase in the risk for colorectal cancer. Moreover, this association could be strengthened by cigarette smoking and family history of cancer. Public Library of Science 2013-04-08 /pmc/articles/PMC3620466/ /pubmed/23593308 http://dx.doi.org/10.1371/journal.pone.0060777 Text en © 2013 Liu et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Liu, Li Zhong, Rong Wei, Sheng Xiang, Hao Chen, Jigui Xie, Duoshuang Yin, Jieyun Zou, Li Sun, Jingwen Chen, Wei Miao, Xiaoping Nie, Shaofa The Leptin Gene Family and Colorectal Cancer: Interaction with Smoking Behavior and Family History of Cancer |
title | The Leptin Gene Family and Colorectal Cancer: Interaction with Smoking Behavior and Family History of Cancer |
title_full | The Leptin Gene Family and Colorectal Cancer: Interaction with Smoking Behavior and Family History of Cancer |
title_fullStr | The Leptin Gene Family and Colorectal Cancer: Interaction with Smoking Behavior and Family History of Cancer |
title_full_unstemmed | The Leptin Gene Family and Colorectal Cancer: Interaction with Smoking Behavior and Family History of Cancer |
title_short | The Leptin Gene Family and Colorectal Cancer: Interaction with Smoking Behavior and Family History of Cancer |
title_sort | leptin gene family and colorectal cancer: interaction with smoking behavior and family history of cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3620466/ https://www.ncbi.nlm.nih.gov/pubmed/23593308 http://dx.doi.org/10.1371/journal.pone.0060777 |
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