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Sequence based analysis of U-2973, a cell line established from a double-hit B-cell lymphoma with concurrent MYC and BCL2 rearrangements

机译:基于序列分析的U-2973,这是一种由双重感染B细胞淋巴瘤建立的细胞系,并发MYC和BCL2重排

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Background Double-hit lymphoma is a complex and highly aggressive sub-type of B-cell lymphoma, which has recently been classified and is an area of active research interest due to the poor prognosis for patients with this disease. It is characterized by the presence of both an activating MYC chromosomal translocation and a simultaneous additional oncogenic translocation, often of the BCL2 gene. Recently, a cell line was established from a patient with this complex lymphoma and analyzed using conventional tools revealing it contains both MYC and BCL2 translocation events. Findings In this work, we reanalyzed the genome of the cell line using next generation whole genome sequencing technology in order to catalogue translocations, insertions and deletions which may contribute to the pathology of this lymphoma type. Conclusions We describe the cell line in much greater detail, and pinpoint the exact locations of the chromosomal breakpoints. We also find several rearrangements within cancer-associated genes, which were not found using conventional tools, suggesting that high throughput sequencing may reveal novel targets for therapy, which could be used concurrently with existing treatments.
机译:背景技术双发性淋巴瘤是B细胞淋巴瘤的一种复杂且高度侵袭性的亚型,由于其对患者的预后不良,最近已被分类,并且是活跃的研究热点。它的特征是存在活化的MYC染色体易位和同时发生的其他致癌性易位,通常是BCL2基因。最近,从患有这种复杂淋巴瘤的患者中建立了一个细胞系,并使用常规工具对其进行了分析,发现该细胞系同时含有MYC和BCL2易位事件。研究结果在这项工作中,我们使用下一代全基因组测序技术重新分析了细胞系的基因组,以便对易位,插入和缺失进行分类,这可能有助于这种淋巴瘤类型的病理。结论我们将更详细地描述细胞系,并查明染色体断裂点的确切位置。我们还发现了与癌症相关的基因内的几种重排,这是使用常规工具无法找到的,这表明高通量测序可能揭示出新的治疗靶标,可与现有治疗同时使用。

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