Germline BAP1 mutations misreported as somatic based on tumor-only testing

被引:0
|
作者
Mohamed H. Abdel-Rahman
Karan Rai
Robert Pilarski
Frederick H. Davidorf
Colleen M. Cebulla
机构
[1] The Ohio State University,Department of Ophthalmology and Visual Science
[2] The Ohio State University,Division of Human Genetics, Department of Internal Medicine and Comprehensive Cancer Center
[3] Menoufiya University,Department of Pathology
来源
Familial Cancer | 2016年 / 15卷
关键词
BAP1; Hereditary cancer predisposition; Familial cancer; Uveal melanoma;
D O I
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中图分类号
学科分类号
摘要
We present three unrelated patients with germline mutations in BAP1 misreported as somatic mutations. All had strong family histories of cancer. One of these patients presented with an invasive breast cancer with the tumor tissue showing partial loss of the mutant rather than the wild type allele, suggesting that the germline BAP1 mutation didn’t contribute to breast cancer development in this patient. This data highlights the importance of sequencing matching germline and tumor DNA for proper assessment of somatic versus germline mutation status. In patients with somatic mutations reported from laboratories carrying out tumor-only genomic testing, the possibility that a variant may be a germline mutation should be considered, especially if the personal and/or family history suggests hereditary cancer predisposition. Since tumor-only testing can reveal germline mutations, ethical issues for patients being tested should be considered including proper consent and genetic counseling.
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页码:327 / 330
页数:3
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