Suppr超能文献

患有乳腺癌的犹太女性中的种系BRCA1 185delAG突变

Germline BRCA1 185delAG mutations in Jewish women with breast cancer.

作者信息

Offit K, Gilewski T, McGuire P, Schluger A, Hampel H, Brown K, Swensen J, Neuhausen S, Skolnick M, Norton L, Goldgar D

机构信息

Clinical Genetics Service, Department of Human Genetics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

出版信息

Lancet. 1996 Jun 15;347(9016):1643-5. doi: 10.1016/s0140-6736(96)91484-1.

Abstract

BACKGROUND

We aimed to find out the proportion of breast cancers in Ashkenazi Jewish women attributable to the frameshift mutation at position 185 involving the deletion of adenine and guanine (185delAG) in the breast cancer gene BRCA1.

METHODS

We studied 107 Ashkenazi Jewish women with breast cancer seen at medical oncology and genetic counseling clinics in New York over a three and a half year period beginning in 1992. 80 of the women were diagnosed before age 42 years; the other 27 were diagnosed between 42 and 50 years and had a positive family history. Genomic DNA testing by PCR amplification was done to identify any 185delAG mutations of the BRCA1 gene.

FINDINGS

Of the 80 women diagnosed before the age of 42 years, 16 (20%, 95% CI 11.2-28.8) were heterozygous for the mutation. All 16 women had at least one first-degree or second-degree relative with breast or ovarian cancer. Of 27 probands diagnosed with breast cancer between the ages of 42 and 50 years who had at least one first-degree relative affected with breast or ovarian cancer, 8 (30%, 95% CI 12-47) had 185delAG mutations.

INTERPRETATION

These data suggest that screening for the 185delAG mutation may be useful in genetic counselling of these women where options for detection and prevention of possible cancers can be discussed.

摘要

背景

我们旨在确定在阿什肯纳兹犹太女性中,归因于乳腺癌基因BRCA1第185位移码突变(涉及腺嘌呤和鸟嘌呤缺失,即185delAG)的乳腺癌比例。

方法

我们研究了1992年开始的三年半时间里,在纽约的医学肿瘤学和遗传咨询诊所就诊的107名患有乳腺癌的阿什肯纳兹犹太女性。其中80名女性在42岁之前被诊断出患有乳腺癌;另外27名女性在42至50岁之间被诊断出患有乳腺癌,且有家族病史。通过聚合酶链反应(PCR)扩增进行基因组DNA检测,以确定BRCA1基因的任何185delAG突变。

研究结果

在42岁之前被诊断出患有乳腺癌的80名女性中,有16名(20%,95%置信区间为11.2 - 28.8)为该突变的杂合子。所有16名女性至少有一位患有乳腺癌或卵巢癌的一级或二级亲属。在27名年龄在42至50岁之间被诊断出患有乳腺癌且至少有一位患有乳腺癌或卵巢癌的一级亲属的先证者中,有8名(30%,95%置信区间为12 - 47)有185delAG突变。

解读

这些数据表明,对185delAG突变进行筛查可能有助于对这些女性进行遗传咨询,在此过程中可以讨论检测和预防可能发生癌症的相关选项。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验