Suppr超能文献

一名转移性膀胱癌患者同时存在胚系和体细胞致病性BAP1变异。

Concurrent germline and somatic pathogenic BAP1 variants in a patient with metastatic bladder cancer.

作者信息

Tesch Megan E, Pater Justin A, Vandekerkhove Gillian, Wang Gang, Binnington Kristin, So Alan I, Wyatt Alexander W, Eigl Bernhard J

机构信息

1Department of Medical Oncology, British Columbia Cancer Agency, Vancouver, BC Canada.

2Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA USA.

出版信息

NPJ Genom Med. 2020 Mar 23;5:12. doi: 10.1038/s41525-020-0121-8. eCollection 2020.

Abstract

Germline pathogenic variants in the BRCA1-associated protein-1 () gene cause the BAP1 tumor predisposition syndrome (TPDS). BAP1 TPDS is associated with an increased risk of uveal and cutaneous melanoma, mesothelioma, renal cell carcinoma, and several other cancer subtypes. Here, we report a germline nonsense variant (c.850G>T, p.Glu284Ter) in a patient with bladder cancer and a strong family history of malignancy. Concurrently, we identified a somatic frameshift variant, and as expected, immunostaining validated the loss of BAP1 protein in patient-derived tumor specimens. Together, these data provide strong evidence of pathogenicity in this case. With the addition of bladder cancer to the tumor types reported with germline mutations, our understanding of the BAP1 TPDS continues to evolve, and may affect future screening and surveillance guidelines.

摘要

乳腺癌1号相关蛋白1(BAP1)基因的种系致病变体导致BAP1肿瘤易感性综合征(TPDS)。BAP1 TPDS与葡萄膜和皮肤黑色素瘤、间皮瘤、肾细胞癌以及其他几种癌症亚型的风险增加相关。在此,我们报告一名膀胱癌患者存在种系无义变体(c.850G>T,p.Glu284Ter),且其有恶性肿瘤的家族史。同时,我们鉴定出一种体细胞移码变体,正如预期的那样,免疫染色证实了患者来源的肿瘤标本中BAP1蛋白缺失。这些数据共同为此病例的致病性提供了有力证据。随着膀胱癌被添加到报道有种系BAP1突变的肿瘤类型中,我们对BAP1 TPDS的理解不断发展,可能会影响未来的筛查和监测指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1056/7089973/9435bbc30711/41525_2020_121_Fig1_HTML.jpg

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