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一种新的种系POLE突变导致一种早发性癌症易感性综合征,类似于遗传性错配修复缺陷。

A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency.

作者信息

Wimmer Katharina, Beilken Andreas, Nustede Rainer, Ripperger Tim, Lamottke Britta, Ure Benno, Steinmann Diana, Reineke-Plaass Tanja, Lehmann Ulrich, Zschocke Johannes, Valle Laura, Fauth Christine, Kratz Christian P

机构信息

Division of Human Genetics, Medical University Innsbruck, Peter-Mayr-Straße 1, 6020, Innsbruck, Austria.

Pediatric Hematology and Oncology, Hannover Medical School, Hannover, Germany.

出版信息

Fam Cancer. 2017 Jan;16(1):67-71. doi: 10.1007/s10689-016-9925-1.

Abstract

In a 14-year-old boy with polyposis and rectosigmoid carcinoma, we identified a novel POLE germline mutation, p.(Val411Leu), previously found as recurrent somatic mutation in 'ultramutated' sporadic cancers. This is the youngest reported cancer patient with polymerase proofreading-associated polyposis indicating that POLE mutation p.(Val411Leu) may confer a more severe phenotype than previously reported POLE and POLD1 germline mutations. The patient had multiple café-au-lait macules and a pilomatricoma mimicking the clinical phenotype of constitutional mismatch repair deficiency. We hypothesize that these skin features may be common to different types of constitutional DNA repair defects associated with polyposis and early-onset cancer.

摘要

在一名患有息肉病和直肠乙状结肠癌的14岁男孩中,我们鉴定出一种新的POLE种系突变,即p.(Val411Leu),该突变先前在“超突变”散发性癌症中作为复发性体细胞突变被发现。这是报道的最年轻的患有聚合酶校对相关息肉病的癌症患者,表明POLE突变p.(Val411Leu)可能导致比先前报道的POLE和POLD1种系突变更严重的表型。该患者有多处咖啡牛奶斑和一个毛母质瘤,模仿了遗传性错配修复缺陷的临床表型。我们推测这些皮肤特征可能是与息肉病和早发性癌症相关的不同类型遗传性DNA修复缺陷所共有的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c43c/5243902/4db4e60fca54/10689_2016_9925_Fig1_HTML.jpg

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