Suppr超能文献

系统性硬化症中广泛的突变和染色体不稳定性塑造了体细胞基因组。

Widespread mutagenesis and chromosomal instability shape somatic genomes in systemic sclerosis.

机构信息

Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC, USA.

University Claude Bernard Lyon 1, INSERM U1052-CNRS UMR5286, Cancer Research Center, Centre Léon Bérard, Lyon, France.

出版信息

Nat Commun. 2024 Oct 15;15(1):8889. doi: 10.1038/s41467-024-53332-z.

Abstract

Systemic sclerosis is a connective tissue disorder characterized by excessive fibrosis that primarily affects women, and can present as a multisystem pathology. Roughly 4-22% of patients with systemic sclerosis develop cancer, which drastically worsens prognosis. However, the mechanisms underlying systemic sclerosis initiation, propagation, and cancer development are poorly understood. We hypothesize that the inflammation and immune response associated with systemic sclerosis can trigger DNA damage, leading to elevated somatic mutagenesis, a hallmark of pre-cancerous tissues. To test our hypothesis, we culture clonal lineages of fibroblasts from the lung tissues of controls and systemic sclerosis patients and compare their mutation burdens and spectra. We find an overall increase in all major mutation types in systemic sclerosis samples compared to control lung samples, from small-scale events such as single base substitutions and insertions/deletions, to chromosome-level changes, including copy-number changes and structural variants. In the genomes of patients with systemic sclerosis, we find evidence of somatic hypermutation or kategis (typically only seen in cancer genomes), we identify mutation signatures closely resembling the error-prone translesion polymerase Polη activity, and observe an activation-induced deaminase-like mutation signature, which overlaps with genomic regions displaying kataegis.

摘要

系统性硬化症是一种结缔组织疾病,其特征是过度纤维化,主要影响女性,并可能表现为多系统病理学。大约有 4-22%的系统性硬化症患者会发展为癌症,这大大恶化了预后。然而,系统性硬化症的起始、传播和癌症发展的机制尚不清楚。我们假设与系统性硬化症相关的炎症和免疫反应会引发 DNA 损伤,导致体细胞突变增加,这是癌前组织的标志。为了验证我们的假设,我们培养了来自对照和系统性硬化症患者肺组织的成纤维细胞克隆谱系,并比较了它们的突变负担和谱。我们发现与对照肺样本相比,系统性硬化症样本中所有主要突变类型的总体增加,从单碱基取代和插入/缺失等小规模事件到染色体水平的变化,包括拷贝数变化和结构变异。在系统性硬化症患者的基因组中,我们发现了体细胞超突变或 kataegis 的证据(通常仅见于癌症基因组),我们鉴定了与易错跨损伤聚合酶 Polη 活性密切相似的突变特征,并观察到激活诱导脱氨酶样突变特征,与显示 kataegis 的基因组区域重叠。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c42/11480385/0f50962b65df/41467_2024_53332_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验