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No evidence of linkage to chromosome 1q42.2–43 in 131 prostate cancer families from the ACTANE Consortium
Genetic linkage studies worldwide have proposed various chromosomal localizations for prostate cancer susceptibility genes. A recent study found evidence for linkage to chromosome 1q42.2–43. The aim of our study was to attempt to confirm these findings by performing linkage analysis in 131 families...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2000
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363442/ https://www.ncbi.nlm.nih.gov/pubmed/11104562 http://dx.doi.org/10.1054/bjoc.2000.1524 |
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author | Singh, R |
author_facet | Singh, R |
author_sort | Singh, R |
collection | PubMed |
description | Genetic linkage studies worldwide have proposed various chromosomal localizations for prostate cancer susceptibility genes. A recent study found evidence for linkage to chromosome 1q42.2–43. The aim of our study was to attempt to confirm these findings by performing linkage analysis in 131 families with multiple prostate cancer cases selected from the ACTANE (Anglo, Canada, Texas, Australia, Norway, EU Biomed) Consortium. Parametric and non-parametric linkage (NPL) analyses were performed. Two-point LOD scores failed to show evidence of linkage at any marker (maximum two-point LOD score = 0.40 at recombination fraction θ = 0.2 with marker D1S2850). Using a multipoint heterogeneity analysis, the estimated proportion of families linked to this putative locus (α) was 0% (95% CI = 0.00–0.33). Non-parametric linkage analysis also found no evidence of linkage (maximum NPL score = –0.12, P = 0.55). This analysis of 131 ACTANE families does not support the presence of a locus for a prostate cancer susceptibility gene at 1q42.2–43. Although we cannot rule out the existence of such a locus, analysis indicates that less than 16% of families could be linked to this region. These findings may be a reflection of the locus heterogeneity involved in this disease indicating that there are still other major susceptibility loci to be identified. © 2000 Cancer Research Campaign http://www.bjcancer.com |
format | Text |
id | pubmed-2363442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23634422009-09-10 No evidence of linkage to chromosome 1q42.2–43 in 131 prostate cancer families from the ACTANE Consortium Singh, R Br J Cancer Regular Article Genetic linkage studies worldwide have proposed various chromosomal localizations for prostate cancer susceptibility genes. A recent study found evidence for linkage to chromosome 1q42.2–43. The aim of our study was to attempt to confirm these findings by performing linkage analysis in 131 families with multiple prostate cancer cases selected from the ACTANE (Anglo, Canada, Texas, Australia, Norway, EU Biomed) Consortium. Parametric and non-parametric linkage (NPL) analyses were performed. Two-point LOD scores failed to show evidence of linkage at any marker (maximum two-point LOD score = 0.40 at recombination fraction θ = 0.2 with marker D1S2850). Using a multipoint heterogeneity analysis, the estimated proportion of families linked to this putative locus (α) was 0% (95% CI = 0.00–0.33). Non-parametric linkage analysis also found no evidence of linkage (maximum NPL score = –0.12, P = 0.55). This analysis of 131 ACTANE families does not support the presence of a locus for a prostate cancer susceptibility gene at 1q42.2–43. Although we cannot rule out the existence of such a locus, analysis indicates that less than 16% of families could be linked to this region. These findings may be a reflection of the locus heterogeneity involved in this disease indicating that there are still other major susceptibility loci to be identified. © 2000 Cancer Research Campaign http://www.bjcancer.com Nature Publishing Group 2000-12 /pmc/articles/PMC2363442/ /pubmed/11104562 http://dx.doi.org/10.1054/bjoc.2000.1524 Text en Copyright © 2000 Cancer Research Campaign 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 | Regular Article Singh, R No evidence of linkage to chromosome 1q42.2–43 in 131 prostate cancer families from the ACTANE Consortium |
title | No evidence of linkage to chromosome 1q42.2–43 in 131 prostate cancer families from the ACTANE Consortium |
title_full | No evidence of linkage to chromosome 1q42.2–43 in 131 prostate cancer families from the ACTANE Consortium |
title_fullStr | No evidence of linkage to chromosome 1q42.2–43 in 131 prostate cancer families from the ACTANE Consortium |
title_full_unstemmed | No evidence of linkage to chromosome 1q42.2–43 in 131 prostate cancer families from the ACTANE Consortium |
title_short | No evidence of linkage to chromosome 1q42.2–43 in 131 prostate cancer families from the ACTANE Consortium |
title_sort | no evidence of linkage to chromosome 1q42.2–43 in 131 prostate cancer families from the actane consortium |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363442/ https://www.ncbi.nlm.nih.gov/pubmed/11104562 http://dx.doi.org/10.1054/bjoc.2000.1524 |
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