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非特异性染色体畸变的遗传和环境关联

Genetic and environmental associations of nonspecific chromosomal aberrations.

作者信息

Hemminki Kari, Niazi Yasmeen, Vodickova Ludmila, Vodicka Pavel, Försti Asta

机构信息

Faculty of Medicine and Biomedical Center in Pilsen, Charles University, Pilsen 32300, Czech Republic.

Division of Cancer Epidemiology, German Cancer Research Centre (DKFZ), Heidelberg 69120, Germany.

出版信息

Mutagenesis. 2025 Mar 15;40(1):30-38. doi: 10.1093/mutage/geae006.

Abstract

Nonspecific structural chromosomal aberrations (CAs) are found in around 1% of circulating lymphocytes from healthy individuals but the frequency may be higher after exposure to carcinogenic chemicals or radiation. CAs have been used in the monitoring of persons exposed to genotoxic agents and radiation. Previous studies on occupationally exposed individuals have shown associations between the frequency of CAs in peripheral blood lymphocytes and subsequent cancer risk. The cause for CA formation is believed to be unrepaired or insufficiently repaired DNA double-strand breaks or other DNA damage, and additionally telomere shortening. CAs include chromosome (CSAs) and chromatid type aberrations (CTAs). In the present review, we first describe the types of CAs, the conventional techniques used for their detection and some aspects of interpreting the results. We then focus on germline genetic variation in the frequency and type of CAs measured in a genome-wide association study in healthy individuals in relation to occupational and smoking-related exposure compared to nonexposed referents. The associations (at P < 10-5) on 1473 healthy individuals were broadly classified in candidate genes from functional pathways related to DNA damage response/repair, including PSMA1, UBR5, RRM2B, PMS2P4, STAG3L4, BOD1, COPRS, and FTO; another group included genes related to apoptosis, cell proliferation, angiogenesis, and tumorigenesis, COPB1, NR2C1, COPRS, RHOT1, ITGB3, SYK, and SEMA6A; a third small group mapped to genes KLF7, SEMA5A and ITGB3 which were related to autistic traits, known to manifest frequent CAs. Dedicated studies on 153 DNA repair genes showed associations for some 30 genes, the expression of which could be modified by the implicated variants. We finally point out that monitoring of CAs is so far the only method of assessing cancer risk in healthy human populations, and the use of the technology should be made more attractive by developing automated performance steps and incorporating artificial intelligence methods into the scoring.

摘要

在健康个体的外周血淋巴细胞中,约1%会出现非特异性结构染色体畸变(CAs),但接触致癌化学物质或辐射后,这一频率可能会更高。CAs已被用于监测接触遗传毒性剂和辐射的人群。此前针对职业暴露个体的研究表明,外周血淋巴细胞中CAs的频率与后续患癌风险之间存在关联。人们认为,CAs形成的原因是未修复或修复不充分的DNA双链断裂或其他DNA损伤,此外还有端粒缩短。CAs包括染色体型畸变(CSAs)和染色单体型畸变(CTAs)。在本综述中,我们首先描述CAs的类型、用于检测它们的传统技术以及结果解读的一些方面。然后,我们关注在一项全基因组关联研究中,健康个体与未暴露对照相比,在职业和吸烟相关暴露情况下,所测量的CAs频率和类型中的种系遗传变异。对1473名健康个体的关联研究(P < 10-5)大致分为与DNA损伤反应/修复相关功能途径的候选基因,包括PSMA1、UBR5、RRM2B、PMS2P( _4 )、STAG3L4、BOD1、COPRS和FTO;另一组包括与细胞凋亡、细胞增殖、血管生成和肿瘤发生相关的基因,COPB1、NR2C1、COPRS、RHOT1、ITGB3、SYK和SEMA6A;第三小组成员映射到与自闭症特征相关已知会频繁出现CAs的基因KLF7、SEMA5A和ITGB3。对153个DNA修复基因的专门研究显示约30个基因存在关联,其表达可能会被相关变异所改变。我们最后指出,目前监测CAs是评估健康人群癌症风险的唯一方法,通过开发自动化操作步骤并将人工智能方法纳入评分,应使该技术的应用更具吸引力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2542/11911008/1b8300a21fdb/geae006_fig1.jpg

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