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胚系 BAP1 突变易患恶性间皮瘤。

Germline BAP1 mutations predispose to malignant mesothelioma.

机构信息

Cancer Biology Program, Fox Chase Cancer Center, Philadelphia, Pennsylvania, USA.

出版信息

Nat Genet. 2011 Aug 28;43(10):1022-5. doi: 10.1038/ng.912.

Abstract

Because only a small fraction of asbestos-exposed individuals develop malignant mesothelioma, and because mesothelioma clustering is observed in some families, we searched for genetic predisposing factors. We discovered germline mutations in the gene encoding BRCA1 associated protein-1 (BAP1) in two families with a high incidence of mesothelioma, and we observed somatic alterations affecting BAP1 in familial mesotheliomas, indicating biallelic inactivation. In addition to mesothelioma, some BAP1 mutation carriers developed uveal melanoma. We also found germline BAP1 mutations in 2 of 26 sporadic mesotheliomas; both individuals with mutant BAP1 were previously diagnosed with uveal melanoma. We also observed somatic truncating BAP1 mutations and aberrant BAP1 expression in sporadic mesotheliomas without germline mutations. These results identify a BAP1-related cancer syndrome that is characterized by mesothelioma and uveal melanoma. We hypothesize that other cancers may also be involved and that mesothelioma predominates upon asbestos exposure. These findings will help to identify individuals at high risk of mesothelioma who could be targeted for early intervention.

摘要

由于只有一小部分接触石棉的个体发展为恶性间皮瘤,并且在一些家族中观察到间皮瘤聚集,因此我们寻找遗传易感性因素。我们在两个间皮瘤发病率高的家族中发现了编码 BRCA1 相关蛋白 1 (BAP1) 的基因突变,并且在家族性间皮瘤中观察到影响 BAP1 的体细胞改变,表明双等位基因失活。除了间皮瘤,一些 BAP1 突变携带者还发生了葡萄膜黑色素瘤。我们还在 26 例散发性间皮瘤中的 2 例中发现了 BAP1 的种系突变;具有突变 BAP1 的个体均以前被诊断为葡萄膜黑色素瘤。我们还观察到散发性间皮瘤中存在无种系突变的体细胞截断 BAP1 突变和异常 BAP1 表达。这些结果确定了一种与 BAP1 相关的癌症综合征,其特征为间皮瘤和葡萄膜黑色素瘤。我们假设其他癌症也可能涉及,并且在接触石棉后间皮瘤占主导地位。这些发现将有助于识别出患有间皮瘤风险较高的个体,这些个体可以进行早期干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60c6/3184199/7446c0726847/nihms-314867-f0001.jpg

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