Medical Radiology and Radiation Safety. 2024. Vol. 69. № 5
DOI:10.33266/1024-6177-2024-69-5-53-58
E.A. Blinova1, 2, A.V. Korechenkova1, M.A. Yanishevskaya1, А.V. Akleyev1, 2
Effect of Repair Gene Polymorphism on the Risk
of Malignant Neoplasm Development after Chronic Radiation Exposure
1 Urals Research Center for Radiation Medicine, Chelyabinsk, Russia
2 Chelyabinsk State University, Chelyabinsk, Russia
Contact person: E.A. Blinova, e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.
Abstract
The efficiency of DNA integrity repair processes after radiation exposure may depend on hereditary variations of repair genes caused by single nucleotide polymorphisms. Disturbances or even failure of repair processes trigger a chain of reactions leading to genome instability and oncogenic transformation of the cell.
Purpose: To investigate the association of single nucleotide polymorphism in genes of nucleotide excision repair (ERCC2 rs13181, XPC rs2228001), AP site repair (APEX rs1130409), homologous recombination (XRCC3 rs861539), single-strand DNA break repair (XRCC1 rs25487), and double-strand DNA break repair (PARP rs1136410, XRCC4 rs2075685) with the risk of malignant neoplasm development of various localisations in chronically exposed persons.
Material and methods: The study was conducted in 861 individuals who were exposed to chronic low dose rate radiation. 274 people of which had malignant neoplasms (MN) of various localisations and 587 people made up the comparison group (exposed persons without MN). The mean accumulated dose to red bone marrow (RBM) in the group of people with MN was 561.65±25.31 mGy, while in the comparison group it was 543.14±36.06 mGy. Genotyping of polymorphic loci rs13181, rs2228001, rs1130409, rs861539, rs25487, rs1136410, and rs2075685 was performed by real-time PCR. The association of polymorphic loci with the risk of MN development was determined by the odds ratio (OR) and 95 % confidence interval (95 % CI). A multifactor dimensionality reduction method was used to assess intergenic interactions.
Results: Single-stranded DNA break repair gene rs25487 (XRCC1) polymorphism in accordance with the dominant model is associated with an increased risk of MN development in the combined group of the examined persons (OR=1.79 (1.12‒2.87), p=0.01). The polymorphism of the gene involved in homologous recombination rs861539 (XRCC3) in accordance with the recessive model is associated with a reduced risk of MN development both in the combined group of exposed persons (OR = 0.25 (0.15‒0.41; p<0.00001), and separately in the group of the Slavs (OR = 0.28 (0.13‒0.60); p<0.0001) and in the group of the Turks (OR = 0.22 (0.11‒0.44; p<0.0001). The model of interfactorial interactions allowed us to establish a protective effect with respect to the risk of MN development in carriers of polymorphic loci rs861539 of XRCC3 gene and rs1130409 of APEX1 gene (p<0.001).
Keywords: chronic radiation exposure, single nucleotide polymorphism, repair genes, malignant neoplasm
For citation: Blinova EA, Korechenkova AV, Yanishevskaya MA, Akleyev АV. Effect of Repair Gene Polymorphism on the Risk of Malignant Neoplasm Development after Chronic Radiation Exposure. Medical Radiology and Radiation Safety. 2024;69(5):53–58. (In Russian). DOI:10.33266/1024-6177-2024-69-5-53-58
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Conflict of interest. The authors declare no conflict of interest.
Financing. The article was prepared as part of the implementation of the federal target program “Ensuring nuclear and radiation safety for 2016-2020 and for the period until 2030” (contract No. 27.501.21.2 dated June 11, 2021).
Contribution. Blinova EA – methodology development, article authoring;
AV Korechenkova – statistical processing, article authoring;
Yanishevskaya MA – laboratory research, article authoring; Akleyev AV — development of the research concept, scientific supervision, article authoring.
Article received: 20.05.2024. Accepted for publication: 25.06.2024.