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Non-IG::MYC in Diffuse Large B-cell Lymphoma Confers Variable Genomic Configurations and MYC Transactivation Potential

Leukemia(2024)

University of Cambridge | Cergentis BV | St James’ University Hospital | Cambridge University Hospitals NHS Foundation Trust | University Hospitals Coventry and Warwickshire NHS Trust | Norfolk and Norwich University Foundation Hospital | Peterborough City Hospital | James Paget University Hospitals NHS Foundation Trust | East Suffolk and North Essex Foundation Trust | University of Leeds | University of Southampton

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Abstract
MYC translocation occurs in 8–14% of diffuse large B-cell lymphoma (DLBCL), and may concur with BCL2 and/or BCL6 translocation, known as double-hit (DH) or triple-hit (TH). DLBCL-MYC/BCL2-DH/TH are largely germinal centre B-cell like subtype, but show variable clinical outcome, with IG::MYC fusion significantly associated with inferior survival. While DLBCL-MYC/BCL6-DH are variable in their cell-of-origin subtypes and clinical outcome. Intriguingly, only 40-50% of DLBCL with MYC translocation show high MYC protein expression (>70%). We studied 186 DLBCLs with MYC translocation including 32 MYC/BCL2/BCL6-TH, 75 MYC/BCL2-DH and 26 MYC/BCL6-DH. FISH revealed a MYC/BCL6 fusion in 59% of DLBCL-MYC/BCL2/BCL6-TH and 27% of DLBCL-MYC/BCL6-DH. Targeted NGS showed a similar mutation profile and LymphGen genetic subtype between DLBCL-MYC/BCL2/BCL6-TH and DLBCL-MYC/BCL2-DH, but variable LymphGen subtypes among DLBCL-MYC/BCL6-DH. MYC protein expression is uniformly high in DLBCL with IG::MYC, but variable in those with non-IG::MYC including MYC/BCL6-fusion. Translocation breakpoint analyses of 8 cases by TLC-based NGS showed no obvious genomic configuration that enables MYC transactivation in 3 of the 4 cases with non-IG::MYC, while a typical promoter substitution or IGH super enhancer juxtaposition in the remaining cases. The findings potentially explain variable MYC expression in DLBCL with MYC translocation, and also bear practical implications in its routine assessment.
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要点】:论文探讨了弥漫性大B细胞淋巴瘤(DLBCL)中非免疫球蛋白(non-IG)::MYC的基因配置和MYC转录激活潜能,揭示了其与临床结局的关联。

方法】:通过荧光原位杂交(FISH)和靶点下一代测序(targeted NGS)技术分析186例MYC易位的DLBCL病例,包括32例三重打击(TH)、75例双重打击(DH)和26例MYC/BCL6-DH病例。

实验】:实验包括对8个病例的易位断裂点分析,使用基于TLC的下一代测序技术,发现non-IG::MYC的基因配置和MYC表达潜能的差异,数据集未明确提及。