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Functional variants of lncRNA LINC00673 and gastric cancer susceptibility: a case-control study in a Chinese population
Background: Two genome-wide association studies (GWASs) identified LINC00673 rs11655237 was associated with susceptibility to pancreatic cancer. Methods: To investigate the association between LINC00673 polymorphisms and gastric cancer (GC) risk, and the impact of gene-environmental interaction on G...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503345/ https://www.ncbi.nlm.nih.gov/pubmed/31118802 http://dx.doi.org/10.2147/CMAR.S187011 |
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author | Zhao, Kexin Zhang, Rui Li, Tiantian Xiong, Zhifan |
author_facet | Zhao, Kexin Zhang, Rui Li, Tiantian Xiong, Zhifan |
author_sort | Zhao, Kexin |
collection | PubMed |
description | Background: Two genome-wide association studies (GWASs) identified LINC00673 rs11655237 was associated with susceptibility to pancreatic cancer. Methods: To investigate the association between LINC00673 polymorphisms and gastric cancer (GC) risk, and the impact of gene-environmental interaction on GC risk, we conducted this case-control study in a Chinese population. Results: We found rs11655237 significantly increased susceptibility of GC in the Chinese population (OR=1.29; 95% CI=1.12–1.48; P=4.1×10(−4)), and a significant interaction was found between rs11655237 and Helicobacter pylori infection (P=0.006). Expression of LINC00673 was significantly higher in adjacent normal tissues than in paired cancer tissues (P<0.001) and significantly lower in the cancer or paired adjacent normal tissues of GC patients with rs11655237 allele A than in those with rs11655237 allele G (P<0.001). Mechanism exploration found that, the construct with the rs11655237[A] allele had significantly reduced luciferase activity in the presence of miR-1231, and this effect could be completely rescued when miR-1231 inhibitor was present. Conclusion: Our results indicate that LINC00673 rs11655237 is associated with an increased GC risk, possibly by down-regulating LINC00673 expression through creating a miR-1231 binding site. |
format | Online Article Text |
id | pubmed-6503345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-65033452019-05-22 Functional variants of lncRNA LINC00673 and gastric cancer susceptibility: a case-control study in a Chinese population Zhao, Kexin Zhang, Rui Li, Tiantian Xiong, Zhifan Cancer Manag Res Original Research Background: Two genome-wide association studies (GWASs) identified LINC00673 rs11655237 was associated with susceptibility to pancreatic cancer. Methods: To investigate the association between LINC00673 polymorphisms and gastric cancer (GC) risk, and the impact of gene-environmental interaction on GC risk, we conducted this case-control study in a Chinese population. Results: We found rs11655237 significantly increased susceptibility of GC in the Chinese population (OR=1.29; 95% CI=1.12–1.48; P=4.1×10(−4)), and a significant interaction was found between rs11655237 and Helicobacter pylori infection (P=0.006). Expression of LINC00673 was significantly higher in adjacent normal tissues than in paired cancer tissues (P<0.001) and significantly lower in the cancer or paired adjacent normal tissues of GC patients with rs11655237 allele A than in those with rs11655237 allele G (P<0.001). Mechanism exploration found that, the construct with the rs11655237[A] allele had significantly reduced luciferase activity in the presence of miR-1231, and this effect could be completely rescued when miR-1231 inhibitor was present. Conclusion: Our results indicate that LINC00673 rs11655237 is associated with an increased GC risk, possibly by down-regulating LINC00673 expression through creating a miR-1231 binding site. Dove 2019-05-01 /pmc/articles/PMC6503345/ /pubmed/31118802 http://dx.doi.org/10.2147/CMAR.S187011 Text en © 2019 Zhao et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Zhao, Kexin Zhang, Rui Li, Tiantian Xiong, Zhifan Functional variants of lncRNA LINC00673 and gastric cancer susceptibility: a case-control study in a Chinese population |
title | Functional variants of lncRNA LINC00673 and gastric cancer susceptibility: a case-control study in a Chinese population |
title_full | Functional variants of lncRNA LINC00673 and gastric cancer susceptibility: a case-control study in a Chinese population |
title_fullStr | Functional variants of lncRNA LINC00673 and gastric cancer susceptibility: a case-control study in a Chinese population |
title_full_unstemmed | Functional variants of lncRNA LINC00673 and gastric cancer susceptibility: a case-control study in a Chinese population |
title_short | Functional variants of lncRNA LINC00673 and gastric cancer susceptibility: a case-control study in a Chinese population |
title_sort | functional variants of lncrna linc00673 and gastric cancer susceptibility: a case-control study in a chinese population |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503345/ https://www.ncbi.nlm.nih.gov/pubmed/31118802 http://dx.doi.org/10.2147/CMAR.S187011 |
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