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揭示影响遗传性错配修复缺陷个体肿瘤突变模式的诱变过程。

Unraveling mutagenic processes influencing the tumor mutational patterns of individuals with constitutional mismatch repair deficiency.

作者信息

Weijers Dilys D, Hinić Snežana, Kroeze Emma, Gorris Mark Aj, Schreibelt Gerty, Middelkamp Sjors, Mensenkamp Arjen R, Bladergroen Reno, Verrijp Kiek, Hoogerbrugge Nicoline, Wesseling Pieter, van der Post Rachel S, Loeffen Jan Lc, Gidding Corrie Em, van Kouwen Mariëtte Ca, de Vries I Jolanda M, van Boxtel Ruben, de Voer Richarda M, Jongmans Marjolijn Cj, Kuiper Roland P

机构信息

Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Department of Human Genetics, Radboud university medical center, Nijmegen, The Netherlands.

出版信息

Nat Commun. 2025 May 14;16(1):4459. doi: 10.1038/s41467-025-59775-2.

Abstract

Constitutional mismatch repair deficiency (CMMRD), caused by bi-allelic germline variants in mismatch repair (MMR) genes, is associated with high cancer incidence early in life. A better understanding of mutational processes driving sequential CMMRD tumors can advance optimal treatment. Here, we describe a genomic characterization on a representative collection of CMMRD-associated tumors consisting of 41 tumors from 17 individuals. Mutational patterns in these tumors appear to be influenced by multiple factors, including the affected MMR gene and tumor type. Somatic polymerase proofreading mutations, commonly present in brain tumors, are also found in a T-cell lymphoblastic lymphoma displaying associated mutational patterns. We show prominent mutational patterns in two second primary hematological malignancies after temozolomide treatment. Furthermore, an indel signature, characterized by one-base pair cytosine insertions in cytosine homopolymers, is found in 54% of tumors. In conclusion, analysis of sequential CMMRD tumors reveals diverse mutational patterns influenced by the affected MMR gene, tumor type and treatment history.

摘要

由错配修复(MMR)基因的双等位基因种系变异引起的体质性错配修复缺陷(CMMRD)与生命早期的高癌症发病率相关。更好地了解驱动连续性CMMRD肿瘤的突变过程有助于推进最佳治疗。在此,我们描述了对一组具有代表性的CMMRD相关肿瘤的基因组特征分析,这些肿瘤包括来自17名个体的41个肿瘤。这些肿瘤中的突变模式似乎受多种因素影响,包括受影响的MMR基因和肿瘤类型。常见于脑肿瘤中的体细胞聚合酶校对突变,也在显示相关突变模式的T细胞淋巴母细胞淋巴瘤中发现。我们展示了替莫唑胺治疗后两种第二原发性血液系统恶性肿瘤中的显著突变模式。此外,在54%的肿瘤中发现了一种插入缺失特征,其特点是在胞嘧啶同聚物中出现单碱基对胞嘧啶插入。总之,对连续性CMMRD肿瘤的分析揭示了受受影响的MMR基因、肿瘤类型和治疗史影响的多种突变模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853c/12078508/afdba153ccb7/41467_2025_59775_Fig1_HTML.jpg

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