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The effect of the I1307K APC polymorphism on the clinicopathological features and natural history of breast cancer

The I1307K polymorphism in APC has been found to predispose to colorectal cancer in Ashkenazi Jews, and has recently been associated with an increased risk for breast cancer in the same population. In that study, we genotyped 205 paraffin-embedded breast cancers from Ashkenazi Jewish women diagnosed...

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Autores principales: Yuan, Z Q, Bégin, L R, Wong, N, Brunet, J-S, Trifiro, M, Gordon, P H, Pinsky, L, Foulkes, W D
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374295/
https://www.ncbi.nlm.nih.gov/pubmed/10555757
http://dx.doi.org/10.1038/sj.bjc.6690775
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author Yuan, Z Q
Bégin, L R
Wong, N
Brunet, J-S
Trifiro, M
Gordon, P H
Pinsky, L
Foulkes, W D
author_facet Yuan, Z Q
Bégin, L R
Wong, N
Brunet, J-S
Trifiro, M
Gordon, P H
Pinsky, L
Foulkes, W D
author_sort Yuan, Z Q
collection PubMed
description The I1307K polymorphism in APC has been found to predispose to colorectal cancer in Ashkenazi Jews, and has recently been associated with an increased risk for breast cancer in the same population. In that study, we genotyped 205 paraffin-embedded breast cancers from Ashkenazi Jewish women diagnosed below the age of 65. We now present an extended analysis, with clinicopathological correlations between carriers of I1307K and non-carriers. Twenty-four of 209 cases (11.5%, 95% confidence interval 7.5–16.6) were found to carry the I1307K polymorphism. When stratifying the data by other relevant clinicopathological variables, we observed no association between the presence of this polymorphism and age at diagnosis (P = 0.52), grade (P = 0.074), tumour size (P = 0.99), lymph node status (P = 0.82), oestrogen receptor status (P = 0.23) or P53 immunoreactivity (P = 0.80). The breast-cancer specific 5-year survival for women with I1307 K polymorphism was 88.9% compared with 81.6% in women without I1307K (P = 0.34). Using microdissected samples and direct sequencing, no somatic mutations were observed in any of the 24 I1307K-positive cases. Single-strand conformation analysis of 158 of the I1307K-negative breast cancers that were available for study revealed no mobility shifts. We conclude that the presence of the I1307K polymorphism does not appear to be associated with any particular clinicopathological feature of breast cancer and importantly, does not affect the prognosis. © 1999 Cancer Research Campaign
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spelling pubmed-23742952009-09-10 The effect of the I1307K APC polymorphism on the clinicopathological features and natural history of breast cancer Yuan, Z Q Bégin, L R Wong, N Brunet, J-S Trifiro, M Gordon, P H Pinsky, L Foulkes, W D Br J Cancer Regular Article The I1307K polymorphism in APC has been found to predispose to colorectal cancer in Ashkenazi Jews, and has recently been associated with an increased risk for breast cancer in the same population. In that study, we genotyped 205 paraffin-embedded breast cancers from Ashkenazi Jewish women diagnosed below the age of 65. We now present an extended analysis, with clinicopathological correlations between carriers of I1307K and non-carriers. Twenty-four of 209 cases (11.5%, 95% confidence interval 7.5–16.6) were found to carry the I1307K polymorphism. When stratifying the data by other relevant clinicopathological variables, we observed no association between the presence of this polymorphism and age at diagnosis (P = 0.52), grade (P = 0.074), tumour size (P = 0.99), lymph node status (P = 0.82), oestrogen receptor status (P = 0.23) or P53 immunoreactivity (P = 0.80). The breast-cancer specific 5-year survival for women with I1307 K polymorphism was 88.9% compared with 81.6% in women without I1307K (P = 0.34). Using microdissected samples and direct sequencing, no somatic mutations were observed in any of the 24 I1307K-positive cases. Single-strand conformation analysis of 158 of the I1307K-negative breast cancers that were available for study revealed no mobility shifts. We conclude that the presence of the I1307K polymorphism does not appear to be associated with any particular clinicopathological feature of breast cancer and importantly, does not affect the prognosis. © 1999 Cancer Research Campaign Nature Publishing Group 1999-11 /pmc/articles/PMC2374295/ /pubmed/10555757 http://dx.doi.org/10.1038/sj.bjc.6690775 Text en Copyright © 1999 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
Yuan, Z Q
Bégin, L R
Wong, N
Brunet, J-S
Trifiro, M
Gordon, P H
Pinsky, L
Foulkes, W D
The effect of the I1307K APC polymorphism on the clinicopathological features and natural history of breast cancer
title The effect of the I1307K APC polymorphism on the clinicopathological features and natural history of breast cancer
title_full The effect of the I1307K APC polymorphism on the clinicopathological features and natural history of breast cancer
title_fullStr The effect of the I1307K APC polymorphism on the clinicopathological features and natural history of breast cancer
title_full_unstemmed The effect of the I1307K APC polymorphism on the clinicopathological features and natural history of breast cancer
title_short The effect of the I1307K APC polymorphism on the clinicopathological features and natural history of breast cancer
title_sort effect of the i1307k apc polymorphism on the clinicopathological features and natural history of breast cancer
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374295/
https://www.ncbi.nlm.nih.gov/pubmed/10555757
http://dx.doi.org/10.1038/sj.bjc.6690775
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