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HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease
The candidate prostate cancer susceptibility gene HPC2/ELAC2 has two common coding polymorphisms: (Ser→Leu 217) and (Ala→Thr 541). The Thr541 variant in the HPC2/ELAC2 gene has previously been reported to be at an increased frequency in prostate cancer cases. To evaluate this hypothesis we genotyped...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2002
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376179/ https://www.ncbi.nlm.nih.gov/pubmed/12373607 http://dx.doi.org/10.1038/sj.bjc.6600564 |
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author | Meitz, J C Edwards, S M Easton, D F Murkin, A Ardern-Jones, A Jackson, R A Williams, S Dearnaley, D P Stratton, M R Houlston, R S Eeles, R A |
author_facet | Meitz, J C Edwards, S M Easton, D F Murkin, A Ardern-Jones, A Jackson, R A Williams, S Dearnaley, D P Stratton, M R Houlston, R S Eeles, R A |
author_sort | Meitz, J C |
collection | PubMed |
description | The candidate prostate cancer susceptibility gene HPC2/ELAC2 has two common coding polymorphisms: (Ser→Leu 217) and (Ala→Thr 541). The Thr541 variant in the HPC2/ELAC2 gene has previously been reported to be at an increased frequency in prostate cancer cases. To evaluate this hypothesis we genotyped 432 prostate cancer patients (including 262 patients diagnosed ⩽55 years) and 469 UK, population based control individuals with no family history of cancer. We found no significant difference in the frequencies of Thr541-containing genotypes between cases and controls (OR=1.41, 95% CI 0.79–2.50). The association remained non-significant when the analysis was restricted to cases divided by age of onset into those diagnosed ⩽55 years (OR=1.50, 95% CI 0.79–2.85) or to patients diagnosed >55 years (OR=1.27, 95% CI 0.59–2.74). We conclude that any association between the Thr541 variant and prostate cancer is likely to be weak. British Journal of Cancer (2002) 87, 905–908. doi:10.1038/sj.bjc.6600564 www.bjcancer.com © 2002 Cancer Research UK |
format | Text |
id | pubmed-2376179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23761792009-09-10 HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease Meitz, J C Edwards, S M Easton, D F Murkin, A Ardern-Jones, A Jackson, R A Williams, S Dearnaley, D P Stratton, M R Houlston, R S Eeles, R A Br J Cancer Genetics and Genomics The candidate prostate cancer susceptibility gene HPC2/ELAC2 has two common coding polymorphisms: (Ser→Leu 217) and (Ala→Thr 541). The Thr541 variant in the HPC2/ELAC2 gene has previously been reported to be at an increased frequency in prostate cancer cases. To evaluate this hypothesis we genotyped 432 prostate cancer patients (including 262 patients diagnosed ⩽55 years) and 469 UK, population based control individuals with no family history of cancer. We found no significant difference in the frequencies of Thr541-containing genotypes between cases and controls (OR=1.41, 95% CI 0.79–2.50). The association remained non-significant when the analysis was restricted to cases divided by age of onset into those diagnosed ⩽55 years (OR=1.50, 95% CI 0.79–2.85) or to patients diagnosed >55 years (OR=1.27, 95% CI 0.59–2.74). We conclude that any association between the Thr541 variant and prostate cancer is likely to be weak. British Journal of Cancer (2002) 87, 905–908. doi:10.1038/sj.bjc.6600564 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-10-07 2002-10-07 /pmc/articles/PMC2376179/ /pubmed/12373607 http://dx.doi.org/10.1038/sj.bjc.6600564 Text en Copyright © 2002 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Genetics and Genomics Meitz, J C Edwards, S M Easton, D F Murkin, A Ardern-Jones, A Jackson, R A Williams, S Dearnaley, D P Stratton, M R Houlston, R S Eeles, R A HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease |
title | HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease |
title_full | HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease |
title_fullStr | HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease |
title_full_unstemmed | HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease |
title_short | HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease |
title_sort | hpc2/elac2 polymorphisms and prostate cancer risk: analysis by age of onset of disease |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376179/ https://www.ncbi.nlm.nih.gov/pubmed/12373607 http://dx.doi.org/10.1038/sj.bjc.6600564 |
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