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Absence of CHEK2 mutations in Spanish families with hereditary breast cancer.

作者信息

Bellosillo Beatriz, Tusquets Ignacio, Longarón Raquel, Pérez-Lezaun Anna, Bellet Meritxell, Fabregat Xavier, Serrano Sergi, Solé Francesc

出版信息

Cancer Genet Cytogenet. 2005 Aug;161(1):93-5. doi: 10.1016/j.cancergencyto.2005.01.016.

DOI:10.1016/j.cancergencyto.2005.01.016
PMID:16080966
Abstract
摘要

相似文献

1
Absence of CHEK2 mutations in Spanish families with hereditary breast cancer.
Cancer Genet Cytogenet. 2005 Aug;161(1):93-5. doi: 10.1016/j.cancergencyto.2005.01.016.
2
Incidence of BRCA1 and BRCA2 mutations in 54 Chilean families with breast/ovarian cancer, genotype-phenotype correlations.54个智利乳腺癌/卵巢癌家族中BRCA1和BRCA2突变的发生率及基因型-表型相关性
Breast Cancer Res Treat. 2006 Jan;95(1):81-7. doi: 10.1007/s10549-005-9047-1. Epub 2005 Oct 27.
3
Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects.西班牙乳腺癌/卵巢癌患者中BRCA1和BRCA2基因分析：西班牙特有的高比例突变及奠基者效应证据
Hum Mutat. 2003 Oct;22(4):301-12. doi: 10.1002/humu.10260.
4
The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families.CHEK2*1100delC变异体在非BRCA1/BRCA2多病例家族中作为乳腺癌风险修饰因子发挥作用。
Cancer Res. 2003 Dec 1;63(23):8153-7.
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Comprehensive genetic characterization of hereditary breast/ovarian cancer families from Slovakia.斯洛伐克遗传性乳腺癌/卵巢癌家系的综合遗传特征分析。
Breast Cancer Res Treat. 2011 Feb;126(1):119-30. doi: 10.1007/s10549-010-1325-x. Epub 2011 Jan 4.
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Intra-abdominal carcinomatosis after prophylactic oophorectomy in women of hereditary breast ovarian cancer syndrome kindreds associated with BRCA1 and BRCA2 mutations.与BRCA1和BRCA2基因突变相关的遗传性乳腺癌卵巢癌综合征家族中女性接受预防性卵巢切除术后的腹腔内癌转移
Gynecol Oncol. 2005 May;97(2):457-67. doi: 10.1016/j.ygyno.2005.01.039.
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[The limited spectrum of pathogenic BRCA1 and BRCA2 mutations in the French Canadian breast and breast-ovarian cancer families, a founder population of Quebec, Canada].[加拿大魁北克奠基人群体法裔加拿大乳腺癌和乳腺-卵巢癌家族中致病性BRCA1和BRCA2突变的有限谱]
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The average cumulative risks of breast and ovarian cancer for carriers of mutations in BRCA1 and BRCA2 attending genetic counseling units in Spain.在西班牙前往遗传咨询机构的BRCA1和BRCA2基因发生突变的携带者患乳腺癌和卵巢癌的平均累积风险。
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Molecular analysis of the BRCA1 and BRCA2 genes in 32 breast and/or ovarian cancer Spanish families.对32个西班牙乳腺癌和/或卵巢癌家族的BRCA1和BRCA2基因进行分子分析。
Br J Cancer. 2000 Apr;82(7):1266-70. doi: 10.1054/bjoc.1999.1089.
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BRCA1/BRCA2 rearrangements and CHEK2 common mutations are infrequent in Italian male breast cancer cases.在意大利男性乳腺癌病例中，BRCA1/BRCA2重排和CHEK2常见突变并不常见。
Breast Cancer Res Treat. 2008 Jul;110(1):161-7. doi: 10.1007/s10549-007-9689-2. Epub 2007 Jul 28.

引用本文的文献

1
Contribution of large genomic rearrangements in BRCA1/2 genes and CHEK2 1100delC allele variant to the development of breast/ovarian cancer in Argentinian population.BRCA1/2基因中的大型基因组重排以及CHEK2 1100delC等位基因变体对阿根廷人群乳腺癌/卵巢癌发生发展的作用。
Breast Cancer Res Treat. 2025 Apr;210(2):385-391. doi: 10.1007/s10549-024-07576-4. Epub 2024 Dec 20.
2
Assessment of pathogenic variation in gynecologic cancer genes in a national cohort.评估全国队列中妇科癌症基因的致病性变异。
Sci Rep. 2023 Mar 31;13(1):5307. doi: 10.1038/s41598-023-32397-8.
3
The *1100delC Mutation and Adolescent Breast Cancer: A Case Report of Breast Cancer in a 19-Year-Old and a Review of the Literature.
1100delC突变与青少年乳腺癌：一例19岁乳腺癌病例报告及文献综述
Breast Care (Basel). 2022 Feb;17(1):85-89. doi: 10.1159/000513679. Epub 2021 Mar 8.
4
The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population.CHEK2基因1100delC等位变异在摩洛哥人群的家族性和散发性乳腺癌病例中不存在。
Springerplus. 2015 Feb 1;4:38. doi: 10.1186/s40064-014-0778-5. eCollection 2015.