Genetic and environmental associations of nonspecific chromosomal aberrations

Author:

Hemminki Kari12ORCID,Niazi Yasmeen34,Vodickova Ludmila156,Vodicka Pavel156,Försti Asta34

Affiliation:

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

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

3. Hopp Children’s Cancer Center (KiTZ) , Heidelberg , Germany

4. Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK) , Heidelberg , Germany

5. Department of Molecular Biology of Cancer, Institute of Experimental Medicine of the Czech Academy of Sciences , Videnska 1083, Prague 14200 , Czech Republic

6. Institute of Biology and Medical Genetics, Charles University , Albertov 4, Prague 12800 , Czech Republic

Abstract

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.

Publisher

Oxford University Press (OUP)

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Frequencies of chromosomal aberrations and related biochemical parameters in welders;Mutation Research - Genetic Toxicology and Environmental Mutagenesis;2024-08

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