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一例BRCA1和BRCA2基因双杂合性的家族性乳腺癌病例。

A case of familial breast cancer with double heterozygosity for BRCA1 and BRCA2 genes.

作者信息

Nomizu Tadashi, Matsuzaki Masami, Katagata Naoto, Kobayashi Yusuke, Sakuma Takeshi, Monma Tomoyuki, Saito Motonobu, Watanabe Fumiaki, Midorikawa Shinichi, Yamaguchi Yoshiko

机构信息

Department of Surgery and Breast Surgery, Hoshi General Hospital, 2-1-16 Omachi, Koriyama, 963-8501, Japan,

出版信息

Breast Cancer. 2015 Sep;22(5):557-61. doi: 10.1007/s12282-012-0432-4. Epub 2012 Dec 15.

Abstract

We report an extremely rare case of familial breast cancer with deleterious germline mutations in both BRCA1 and BRCA2 genes, of which, to date, no such case has been reported among Japanese breast/ovarian cancer patients. Genetic testing of the family members indicated that the same double heterozygosity for BRCA1 and BRCA2 genes was transmitted to the paternal cousin, and the same BRCA2 mutation to the younger sister with bilateral breast cancer, younger brother with stomach cancer, and proband's son and daughter without cancer. Immunohistochemical analysis of BRCA protein expression was performed using breast cancer tissues from the proband with double heterozygosity for BRCA1 and BRCA2 genes and from her sibling without BRCA1 mutation but with BRCA2 mutation. There was no staining of either BRCA in the proband and no staining of BRCA2 in the sibling.

摘要

我们报告了一例极为罕见的家族性乳腺癌病例,该病例的BRCA1和BRCA2基因均存在有害的种系突变,迄今为止,在日本乳腺癌/卵巢癌患者中尚未报告过此类病例。对家庭成员的基因检测表明,BRCA1和BRCA2基因相同的双杂合性被传递给了父系表亲,相同的BRCA2突变被传递给了患有双侧乳腺癌的妹妹、患有胃癌的弟弟以及先证者未患癌症的儿子和女儿。使用来自具有BRCA1和BRCA2基因双杂合性的先证者及其无BRCA1突变但有BRCA2突变的同胞的乳腺癌组织进行了BRCA蛋白表达的免疫组化分析。先证者中BRCA均无染色,同胞中BRCA2无染色。

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