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在波兰发现 BRCA1 基因中首个反复出现的大型基因组重排。

First recurrent large genomic rearrangement in the BRCA1 gene found in Poland.

机构信息

Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.

Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.

出版信息

Cancer Epidemiol. 2014 Aug;38(4):382-5. doi: 10.1016/j.canep.2014.05.010. Epub 2014 Jun 16.

Abstract

Mutation in the BRCA1 gene increases the risk of the person developing breast and/or ovarian cancer. The prevalence and spectrum of large genomic rearrangements (LGRs) varies considerably among different tested populations. In our previous study we described three LGRs in BRCA1 (exons 13-19, exon 17 and exon 22) in Polish families at high risk of breast and ovarian cancer. In this study we analyzed a group of 550 unselected women with ovarian cancer for the three previously identified LGRs. We used a rapid, single-step and closed-tube method: high-resolution melting analysis (HRMA). In this group of unrelated patients diagnosed with ovarian cancer we found three cases with the same deletions of exon 22. This is the first recurrent large deletion in BRCA1 found in Poland. We conclude that screening for the exon 22 deletion in BRCA1 should be included in the Polish BRCA1 genetic testing panel and possibly extended into other Slavic populations.

摘要

BRCA1 基因突变会增加个体罹患乳腺癌和/或卵巢癌的风险。不同检测人群中,大基因组重排(LGRs)的发生率和谱存在显著差异。在我们之前的研究中,我们描述了波兰高乳腺癌和卵巢癌风险家族中 BRCA1 的三个 LGRs(外显子 13-19、外显子 17 和外显子 22)。在这项研究中,我们使用高分辨率熔解分析(HRMA)对 550 名未经选择的卵巢癌女性进行了之前确定的三个 LGRs 分析。在这组无相关关系的卵巢癌患者中,我们发现了三个具有相同外显子 22 缺失的病例。这是在波兰首次发现 BRCA1 中的复发性大片段缺失。我们得出结论,BRCA1 外显子 22 缺失的筛查应纳入波兰 BRCA1 遗传检测面板,并可能扩展到其他斯拉夫人群。

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