Cargando…

Murine Double-Minute 2 Homolog Single Nucleotide Polymorphisms 285 and 309 in Cervical Carcinogenesis

BACKGROUND AND OBJECTIVE: In Caucasians, the MDM2 single nucleotide polymorphism (SNP) 285 G>C (rs117039649) neutralizes the effect of 309 T>G (rs2279744), which increases MDM2 expression and impairs the p53 pathway. In this study, we examined the distribution of these two SNPs in Polish women...

Descripción completa

Detalles Bibliográficos
Autores principales: Roszak, Andrzej, Misztal, Matthew, Sowińska, Anna, Jagodziński, Pawel P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529876/
https://www.ncbi.nlm.nih.gov/pubmed/26224627
http://dx.doi.org/10.1007/s40291-015-0153-4
_version_ 1782384831243485184
author Roszak, Andrzej
Misztal, Matthew
Sowińska, Anna
Jagodziński, Pawel P.
author_facet Roszak, Andrzej
Misztal, Matthew
Sowińska, Anna
Jagodziński, Pawel P.
author_sort Roszak, Andrzej
collection PubMed
description BACKGROUND AND OBJECTIVE: In Caucasians, the MDM2 single nucleotide polymorphism (SNP) 285 G>C (rs117039649) neutralizes the effect of 309 T>G (rs2279744), which increases MDM2 expression and impairs the p53 pathway. In this study, we examined the distribution of these two SNPs in Polish women with squamous cell carcinoma (SCC) (n = 379), adenocarcinoma (n = 59) and other cervical tumor types (n = 18). METHODS: The polymerase chain reaction-restriction fragment length polymorphism technique and DNA sequencing were employed in our study. RESULTS: The P trend value calculated for the MDM2 285 G>C polymorphism was statistically significant (P(trend) = 0.016) for SCC. Using logistical regression analysis adjusted for the effect of age, pregnancy, oral contraceptive use, tobacco smoking, and menopausal status, we observed that the MDM2 285 G>C SNP protected against SCC, with an adjusted odd ratio (OR) for the C carriers versus G/G genotype of 0.536 (P = 0.019). Stratified analyses of MDM2 285 G>C revealed a protective role of the C allele against SCC in women with a positive history of oral contraceptive use (age-adjusted OR 0.413, P = 0.021) and in premenopausal women (age-adjusted OR 0.362, P = 0.022). We also found that the 285GG/309GG vs 285GG/309 TT genotype increased the risk of SCC (adjusted OR 1.890, P = 0.005). However, the 285CC/309GG + 285GC/309GG versus 285GG/309GG genotype reduced the risk of SCC (adjusted OR 0.311, P = 0.004). CONCLUSION: Our results demonstrate that the MDM2 285C gene variant and 285CC/309GG + 285GC/309GG genotypes protect against SCC, most likely by neutralizing the effect of the 309 T>G SNP. The 285GG/309GG genotype increases the risk of SCC possibly due to increased MDM2 expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40291-015-0153-4) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4529876
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Springer International Publishing
record_format MEDLINE/PubMed
spelling pubmed-45298762015-08-11 Murine Double-Minute 2 Homolog Single Nucleotide Polymorphisms 285 and 309 in Cervical Carcinogenesis Roszak, Andrzej Misztal, Matthew Sowińska, Anna Jagodziński, Pawel P. Mol Diagn Ther Original Research Article BACKGROUND AND OBJECTIVE: In Caucasians, the MDM2 single nucleotide polymorphism (SNP) 285 G>C (rs117039649) neutralizes the effect of 309 T>G (rs2279744), which increases MDM2 expression and impairs the p53 pathway. In this study, we examined the distribution of these two SNPs in Polish women with squamous cell carcinoma (SCC) (n = 379), adenocarcinoma (n = 59) and other cervical tumor types (n = 18). METHODS: The polymerase chain reaction-restriction fragment length polymorphism technique and DNA sequencing were employed in our study. RESULTS: The P trend value calculated for the MDM2 285 G>C polymorphism was statistically significant (P(trend) = 0.016) for SCC. Using logistical regression analysis adjusted for the effect of age, pregnancy, oral contraceptive use, tobacco smoking, and menopausal status, we observed that the MDM2 285 G>C SNP protected against SCC, with an adjusted odd ratio (OR) for the C carriers versus G/G genotype of 0.536 (P = 0.019). Stratified analyses of MDM2 285 G>C revealed a protective role of the C allele against SCC in women with a positive history of oral contraceptive use (age-adjusted OR 0.413, P = 0.021) and in premenopausal women (age-adjusted OR 0.362, P = 0.022). We also found that the 285GG/309GG vs 285GG/309 TT genotype increased the risk of SCC (adjusted OR 1.890, P = 0.005). However, the 285CC/309GG + 285GC/309GG versus 285GG/309GG genotype reduced the risk of SCC (adjusted OR 0.311, P = 0.004). CONCLUSION: Our results demonstrate that the MDM2 285C gene variant and 285CC/309GG + 285GC/309GG genotypes protect against SCC, most likely by neutralizing the effect of the 309 T>G SNP. The 285GG/309GG genotype increases the risk of SCC possibly due to increased MDM2 expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40291-015-0153-4) contains supplementary material, which is available to authorized users. Springer International Publishing 2015-07-30 2015 /pmc/articles/PMC4529876/ /pubmed/26224627 http://dx.doi.org/10.1007/s40291-015-0153-4 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research Article
Roszak, Andrzej
Misztal, Matthew
Sowińska, Anna
Jagodziński, Pawel P.
Murine Double-Minute 2 Homolog Single Nucleotide Polymorphisms 285 and 309 in Cervical Carcinogenesis
title Murine Double-Minute 2 Homolog Single Nucleotide Polymorphisms 285 and 309 in Cervical Carcinogenesis
title_full Murine Double-Minute 2 Homolog Single Nucleotide Polymorphisms 285 and 309 in Cervical Carcinogenesis
title_fullStr Murine Double-Minute 2 Homolog Single Nucleotide Polymorphisms 285 and 309 in Cervical Carcinogenesis
title_full_unstemmed Murine Double-Minute 2 Homolog Single Nucleotide Polymorphisms 285 and 309 in Cervical Carcinogenesis
title_short Murine Double-Minute 2 Homolog Single Nucleotide Polymorphisms 285 and 309 in Cervical Carcinogenesis
title_sort murine double-minute 2 homolog single nucleotide polymorphisms 285 and 309 in cervical carcinogenesis
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529876/
https://www.ncbi.nlm.nih.gov/pubmed/26224627
http://dx.doi.org/10.1007/s40291-015-0153-4
work_keys_str_mv AT roszakandrzej murinedoubleminute2homologsinglenucleotidepolymorphisms285and309incervicalcarcinogenesis
AT misztalmatthew murinedoubleminute2homologsinglenucleotidepolymorphisms285and309incervicalcarcinogenesis
AT sowinskaanna murinedoubleminute2homologsinglenucleotidepolymorphisms285and309incervicalcarcinogenesis
AT jagodzinskipawelp murinedoubleminute2homologsinglenucleotidepolymorphisms285and309incervicalcarcinogenesis