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端粒损耗成为衰老造血和白血病发生过程中克隆选择的一种机制。

Telomere attrition becomes an instrument for clonal selection in aging hematopoiesis and leukemogenesis.

作者信息

McLoughlin Matthew A, Cheloor Kovilakam Sruthi, Dunn William G, Gu Muxin, Tobin Jake, Pershad Yash, Williams Nicholas, Leongamornlert Daniel, Dawson Kevin, Bond Laura, Marando Ludovica, Wen Sean, Wilson Rachael, Valenzano Giampiero, Symeonidou Vasiliki, Rak Justyna, Damaskou Aristi, Gozdecka Malgorzata, Liu Xiaoxuan, Barcena Clea, Nomdedeu Josep, Costeas Paul, Dimitriou Ioannis D, Fiorillo Edoardo, Orrù Valeria, de Almeida Jose Guilherme, McKerrell Thomas, Cullen Matthew, Mohorianu Irina, Foukaneli Theodora, Warren Alan J, Wong Chi, Follows George, Godfrey Anna L, Gudgin Emma, Cucca Francesco, McKinney Eoin, Baxter E Joanna, Gerstung Moritz, Mitchell Jonathan, Wiseman Daniel, Bick Alexander G, Fabre Margarete, Quiros Pedro M, Nangalia Jyoti, Kar Siddhartha, Vassiliou George S

机构信息

Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.

Department of Haematology, University of Cambridge, Cambridge, UK.

出版信息

Nat Genet. 2025 Aug 28. doi: 10.1038/s41588-025-02296-x.

Abstract

The mechanisms through which mutations in splicing factor genes drive clonal hematopoiesis (CH) and myeloid malignancies, and their close association with advanced age, remain poorly understood. Here we show that telomere maintenance plays an important role in this phenomenon. First, by studying 454,098 UK Biobank participants, we find that, unlike most CH subtypes, splicing-factor-mutant CH is more common in those with shorter genetically predicted telomeres, as is CH with mutations in PPM1D and the TERT gene promoter. We go on to show that telomere attrition becomes an instrument for clonal selection in advanced age, with splicing factor mutations 'rescuing' HSCs from critical telomere shortening. Our findings expose the lifelong influence of telomere maintenance on hematopoiesis and identify a potential shared mechanism through which different splicing factor mutations drive leukemogenesis. Understanding the mechanistic basis of these observations can open new therapeutic avenues against splicing-factor-mutant CH and hematological or other cancers.

摘要

剪接因子基因突变驱动克隆性造血(CH)和髓系恶性肿瘤的机制,以及它们与高龄的密切关联,目前仍知之甚少。在此我们表明,端粒维持在这一现象中起重要作用。首先,通过研究454,098名英国生物银行参与者,我们发现,与大多数CH亚型不同,剪接因子突变型CH在遗传预测端粒较短的人群中更为常见,PPM1D和TERT基因启动子发生突变的CH也是如此。我们进而表明,端粒损耗成为高龄时克隆选择的一种手段,剪接因子突变可将造血干细胞从严重的端粒缩短中“拯救”出来。我们的发现揭示了端粒维持对造血的终身影响,并确定了不同剪接因子突变驱动白血病发生的潜在共同机制。了解这些观察结果的机制基础可为针对剪接因子突变型CH以及血液或其他癌症开辟新治疗途径。

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