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具有 11q 异常的伯基特样淋巴瘤的突变景观与伯基特淋巴瘤不同。

The mutational landscape of Burkitt-like lymphoma with 11q aberration is distinct from that of Burkitt lymphoma.

机构信息

Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.

Institute of Human Genetics, Christian-Albrechts University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.

出版信息

Blood. 2019 Feb 28;133(9):962-966. doi: 10.1182/blood-2018-07-864025. Epub 2018 Dec 19.

Abstract

The new recently described provisional lymphoma category Burkitt-like lymphoma with 11q aberration comprises cases similar to Burkitt lymphoma (BL) on morphological, immunophenotypic and gene-expression levels but lacking the IG- translocation. They are characterized by a peculiar imbalance pattern on chromosome 11, but the landscape of mutations is not yet described. Thus, we investigated 15 -negative Burkitt-like lymphoma with 11q aberration (mnBLL,11q,) cases by copy-number analysis and whole-exome sequencing. We refined the regions of 11q imbalance and identified the INO80 complex-associated gene as a positional candidate in 11q24.3. Next to recurrent gains in 12q13.11-q24.32 and 7q34-qter as well as losses in 13q32.3-q34, we identified 47 genes recurrently affected by protein-changing mutations (each ≥3 of 15 cases). Strikingly, we did not detect recurrent mutations in genes of the ID3-TCF3 axis or the SWI/SNF complex that are frequently altered in BL, or in genes frequently mutated in germinal center-derived B-cell lymphomas like or An exception is , which was mutated in 7 of 15 cases. We conclude that the genomic landscape of mnBLL,11q, differs from that of BL both at the chromosomal and mutational levels. Our findings implicate that mnBLL,11q, is a lymphoma category distinct from BL at the molecular level.

摘要

新描述的具有 11q 异常的暂定淋巴瘤类别 Burkitt 样淋巴瘤包括在形态学、免疫表型和基因表达水平上类似于 Burkitt 淋巴瘤 (BL)但缺乏 IG-易位的病例。它们的特点是在 11 号染色体上存在一种特殊的不平衡模式,但突变的景观尚未描述。因此,我们通过拷贝数分析和全外显子组测序研究了 15 例阴性 Burkitt 样淋巴瘤伴 11q 异常 (mnBLL,11q,)。我们细化了 11q 不平衡的区域,并确定了 INO80 复合物相关基因 作为 11q24.3 中的位置候选基因。除了 12q13.11-q24.32 和 7q34-qter 的频繁增益和 13q32.3-q34 的缺失外,我们还鉴定了 47 个经常受到蛋白改变突变影响的基因(每个≥15 例中的 3 个)。引人注目的是,我们没有检测到 ID3-TCF3 轴或 SWI/SNF 复合物中经常在 BL 中改变的基因或在生发中心衍生的 B 细胞淋巴瘤中经常突变的基因,如 或 。一个例外是 ,在 7 例中有突变。我们得出结论,mnBLL,11q,的基因组景观在染色体和突变水平上均与 BL 不同。我们的研究结果表明,mnBLL,11q,在分子水平上是一种与 BL 不同的淋巴瘤类别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1908/6396176/5eeb48fe484a/blood864025absf1.jpg

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