Cargando…
Impact of LMP7 (rs2071543) gene polymorphism in increasing cancer risk: evidence from a meta-analysis and trial sequential analysis
Genetic variant LMP7 (low molecular weight polypeptide 7) –145 C > A may influence the function of immune surveillance of an individual and lead to cancer development. Various studies have investigated the relevance of LMP7 –145 C > A gene polymorphism with cancer risk; but, their results are...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814233/ https://www.ncbi.nlm.nih.gov/pubmed/29464093 http://dx.doi.org/10.18632/oncotarget.23547 |
_version_ | 1783300308411088896 |
---|---|
author | Mandal, Raju K. Dar, Sajad A. Jawed, Arshad Wahid, Mohd Lohani, Mohtashim Panda, Aditya K. Mishra, Bhartendu N. Akhter, Naseem Areeshi, Mohammed Y. Haque, Shafiul |
author_facet | Mandal, Raju K. Dar, Sajad A. Jawed, Arshad Wahid, Mohd Lohani, Mohtashim Panda, Aditya K. Mishra, Bhartendu N. Akhter, Naseem Areeshi, Mohammed Y. Haque, Shafiul |
author_sort | Mandal, Raju K. |
collection | PubMed |
description | Genetic variant LMP7 (low molecular weight polypeptide 7) –145 C > A may influence the function of immune surveillance of an individual and lead to cancer development. Various studies have investigated the relevance of LMP7 –145 C > A gene polymorphism with cancer risk; but, their results are conflicting and inconsistent. To obtain a comprehensive conclusion, a meta-analysis was performed by including eight eligible published studies retrieved from PubMed (Medline), EMBASE and Google Scholar web search until December 2016. Individuals with AA genotype (AA vs CC: p = 0.001; OR = 2.602, 95% CI = 1.780 to 3.803) of LMP7 -145 C > A were found to have 2 folds higher risk of cancer than those with CC genotype. The recessive genetic model (AA vs AC + CC) also indicated that individuals with AA genotype have 2 folds higher cancer risk than AC and CC genotypes (p = 0.001; OR = 2.216, 95% CI = 1.525 to 3.221). Also, significant increased cancer risk was observed in Asians but not in Caucasians. No publication bias was observed during the analysis. Trial sequential analysis also strengthened our current findings. These results suggest that genetic variant LMP7–145 C > A has significant role in increasing cancer risk in overall and Asian population, and could be useful as a prognostic marker for early cancer predisposition. |
format | Online Article Text |
id | pubmed-5814233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-58142332018-02-20 Impact of LMP7 (rs2071543) gene polymorphism in increasing cancer risk: evidence from a meta-analysis and trial sequential analysis Mandal, Raju K. Dar, Sajad A. Jawed, Arshad Wahid, Mohd Lohani, Mohtashim Panda, Aditya K. Mishra, Bhartendu N. Akhter, Naseem Areeshi, Mohammed Y. Haque, Shafiul Oncotarget Meta-Analysis Genetic variant LMP7 (low molecular weight polypeptide 7) –145 C > A may influence the function of immune surveillance of an individual and lead to cancer development. Various studies have investigated the relevance of LMP7 –145 C > A gene polymorphism with cancer risk; but, their results are conflicting and inconsistent. To obtain a comprehensive conclusion, a meta-analysis was performed by including eight eligible published studies retrieved from PubMed (Medline), EMBASE and Google Scholar web search until December 2016. Individuals with AA genotype (AA vs CC: p = 0.001; OR = 2.602, 95% CI = 1.780 to 3.803) of LMP7 -145 C > A were found to have 2 folds higher risk of cancer than those with CC genotype. The recessive genetic model (AA vs AC + CC) also indicated that individuals with AA genotype have 2 folds higher cancer risk than AC and CC genotypes (p = 0.001; OR = 2.216, 95% CI = 1.525 to 3.221). Also, significant increased cancer risk was observed in Asians but not in Caucasians. No publication bias was observed during the analysis. Trial sequential analysis also strengthened our current findings. These results suggest that genetic variant LMP7–145 C > A has significant role in increasing cancer risk in overall and Asian population, and could be useful as a prognostic marker for early cancer predisposition. Impact Journals LLC 2017-12-21 /pmc/articles/PMC5814233/ /pubmed/29464093 http://dx.doi.org/10.18632/oncotarget.23547 Text en Copyright: © 2018 Mandal et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Meta-Analysis Mandal, Raju K. Dar, Sajad A. Jawed, Arshad Wahid, Mohd Lohani, Mohtashim Panda, Aditya K. Mishra, Bhartendu N. Akhter, Naseem Areeshi, Mohammed Y. Haque, Shafiul Impact of LMP7 (rs2071543) gene polymorphism in increasing cancer risk: evidence from a meta-analysis and trial sequential analysis |
title | Impact of LMP7 (rs2071543) gene polymorphism in increasing cancer risk: evidence from a meta-analysis and trial sequential analysis |
title_full | Impact of LMP7 (rs2071543) gene polymorphism in increasing cancer risk: evidence from a meta-analysis and trial sequential analysis |
title_fullStr | Impact of LMP7 (rs2071543) gene polymorphism in increasing cancer risk: evidence from a meta-analysis and trial sequential analysis |
title_full_unstemmed | Impact of LMP7 (rs2071543) gene polymorphism in increasing cancer risk: evidence from a meta-analysis and trial sequential analysis |
title_short | Impact of LMP7 (rs2071543) gene polymorphism in increasing cancer risk: evidence from a meta-analysis and trial sequential analysis |
title_sort | impact of lmp7 (rs2071543) gene polymorphism in increasing cancer risk: evidence from a meta-analysis and trial sequential analysis |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814233/ https://www.ncbi.nlm.nih.gov/pubmed/29464093 http://dx.doi.org/10.18632/oncotarget.23547 |
work_keys_str_mv | AT mandalrajuk impactoflmp7rs2071543genepolymorphisminincreasingcancerriskevidencefromametaanalysisandtrialsequentialanalysis AT darsajada impactoflmp7rs2071543genepolymorphisminincreasingcancerriskevidencefromametaanalysisandtrialsequentialanalysis AT jawedarshad impactoflmp7rs2071543genepolymorphisminincreasingcancerriskevidencefromametaanalysisandtrialsequentialanalysis AT wahidmohd impactoflmp7rs2071543genepolymorphisminincreasingcancerriskevidencefromametaanalysisandtrialsequentialanalysis AT lohanimohtashim impactoflmp7rs2071543genepolymorphisminincreasingcancerriskevidencefromametaanalysisandtrialsequentialanalysis AT pandaadityak impactoflmp7rs2071543genepolymorphisminincreasingcancerriskevidencefromametaanalysisandtrialsequentialanalysis AT mishrabhartendun impactoflmp7rs2071543genepolymorphisminincreasingcancerriskevidencefromametaanalysisandtrialsequentialanalysis AT akhternaseem impactoflmp7rs2071543genepolymorphisminincreasingcancerriskevidencefromametaanalysisandtrialsequentialanalysis AT areeshimohammedy impactoflmp7rs2071543genepolymorphisminincreasingcancerriskevidencefromametaanalysisandtrialsequentialanalysis AT haqueshafiul impactoflmp7rs2071543genepolymorphisminincreasingcancerriskevidencefromametaanalysisandtrialsequentialanalysis |