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Susceptibility of gastric cancer according to leptin and leptin receptor gene polymorphisms in Korea
PURPOSE: Leptin plays an important role in the control of body weight and also has a growth-factor-like function in epithelial cells. Abnormal expression of leptin and leptin receptor may be associated with cancer development and progression. We evaluated the relationship among leptin and leptin rec...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Surgical Society
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392320/ https://www.ncbi.nlm.nih.gov/pubmed/22792528 http://dx.doi.org/10.4174/jkss.2012.83.1.7 |
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author | Kim, Eun-Young Chin, Hyung-Min Park, Seung-Man Jeon, Hae-Myung Chung, Woo-Chul Paik, Chang-Nyol Jun, Kyong-Hwa |
author_facet | Kim, Eun-Young Chin, Hyung-Min Park, Seung-Man Jeon, Hae-Myung Chung, Woo-Chul Paik, Chang-Nyol Jun, Kyong-Hwa |
author_sort | Kim, Eun-Young |
collection | PubMed |
description | PURPOSE: Leptin plays an important role in the control of body weight and also has a growth-factor-like function in epithelial cells. Abnormal expression of leptin and leptin receptor may be associated with cancer development and progression. We evaluated the relationship among leptin and leptin receptors polymorphisms, body mass index (BMI), serum leptin concentrations, and clinicopathologic features with gastric cancer and determined whether they could be the risk factor of gastric cancer. METHODS: We measured the serum leptin concentrations of 48 Korean patients with gastric cancer and 48 age- and sex-matched controls. By polymerase chain reaction-restriction fragment length polymorphism, we investigated one leptin gene promoter G-2548A genotype and four leptin receptor gene polymorphisms at codons 223, 109, 343, and 656. RESULTS: There was no significant difference between the mean leptin concentrations of the patient and control groups, while BMI was significantly lower in gastric cancer cases (22.9 ± 3.6 vs. 24.5 ± 2.8 kg/m(2), P = 0.021). There was significant association between the LEPR Lys109Arg genotype and gastric cancer risk, heterozygotes for GA genotype had been proved to increased the risk of gastric cancer, and its corresponding odds ratio was 2.926 (95% confidence interval, 1.248 to 6.861). CONCLUSION: Our results suggested that LEPR gene Lys109Arg polymorphism is associated with gastric cancer in Korean patients. |
format | Online Article Text |
id | pubmed-3392320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Korean Surgical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-33923202012-07-12 Susceptibility of gastric cancer according to leptin and leptin receptor gene polymorphisms in Korea Kim, Eun-Young Chin, Hyung-Min Park, Seung-Man Jeon, Hae-Myung Chung, Woo-Chul Paik, Chang-Nyol Jun, Kyong-Hwa J Korean Surg Soc Original Article PURPOSE: Leptin plays an important role in the control of body weight and also has a growth-factor-like function in epithelial cells. Abnormal expression of leptin and leptin receptor may be associated with cancer development and progression. We evaluated the relationship among leptin and leptin receptors polymorphisms, body mass index (BMI), serum leptin concentrations, and clinicopathologic features with gastric cancer and determined whether they could be the risk factor of gastric cancer. METHODS: We measured the serum leptin concentrations of 48 Korean patients with gastric cancer and 48 age- and sex-matched controls. By polymerase chain reaction-restriction fragment length polymorphism, we investigated one leptin gene promoter G-2548A genotype and four leptin receptor gene polymorphisms at codons 223, 109, 343, and 656. RESULTS: There was no significant difference between the mean leptin concentrations of the patient and control groups, while BMI was significantly lower in gastric cancer cases (22.9 ± 3.6 vs. 24.5 ± 2.8 kg/m(2), P = 0.021). There was significant association between the LEPR Lys109Arg genotype and gastric cancer risk, heterozygotes for GA genotype had been proved to increased the risk of gastric cancer, and its corresponding odds ratio was 2.926 (95% confidence interval, 1.248 to 6.861). CONCLUSION: Our results suggested that LEPR gene Lys109Arg polymorphism is associated with gastric cancer in Korean patients. The Korean Surgical Society 2012-07 2012-06-26 /pmc/articles/PMC3392320/ /pubmed/22792528 http://dx.doi.org/10.4174/jkss.2012.83.1.7 Text en Copyright © 2012, the Korean Surgical Society http://creativecommons.org/licenses/by-nc/3.0 Journal of the Korean Surgical Society is an Open Access Journal. All articles are distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Eun-Young Chin, Hyung-Min Park, Seung-Man Jeon, Hae-Myung Chung, Woo-Chul Paik, Chang-Nyol Jun, Kyong-Hwa Susceptibility of gastric cancer according to leptin and leptin receptor gene polymorphisms in Korea |
title | Susceptibility of gastric cancer according to leptin and leptin receptor gene polymorphisms in Korea |
title_full | Susceptibility of gastric cancer according to leptin and leptin receptor gene polymorphisms in Korea |
title_fullStr | Susceptibility of gastric cancer according to leptin and leptin receptor gene polymorphisms in Korea |
title_full_unstemmed | Susceptibility of gastric cancer according to leptin and leptin receptor gene polymorphisms in Korea |
title_short | Susceptibility of gastric cancer according to leptin and leptin receptor gene polymorphisms in Korea |
title_sort | susceptibility of gastric cancer according to leptin and leptin receptor gene polymorphisms in korea |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392320/ https://www.ncbi.nlm.nih.gov/pubmed/22792528 http://dx.doi.org/10.4174/jkss.2012.83.1.7 |
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