Association of base excision repair pathway genes OGG1, XRCC1 and MUTYH polymorphisms and the level of 8-oxo-guanine with increased risk of colorectal cancer occurrence
In this work authors investigate influence of selected polymorphisms of DNA repair genes (XRCC1, OGG1 and MUTYH) and level of oxidative damage (measured as level of 8-oxo-guanine, 8-oG) on modulation of the risk of colorectal cancer. The relationship between mutations in the DNA Mismatch Repair (MMR...
Saved in:
Published in | International journal of occupational medicine and environmental health Vol. 35; no. 5; pp. 625 - 633 |
---|---|
Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Heidelberg
Nofer Institute of Occupational Medicine
01.01.2022
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | In this work authors investigate influence of selected polymorphisms of DNA repair genes (XRCC1, OGG1 and MUTYH) and level of oxidative damage (measured as level of 8-oxo-guanine, 8-oG) on modulation of the risk of colorectal cancer. The relationship between mutations in the DNA Mismatch Repair (MMR) genes and the increased risk of hereditary nonpolyposis colorectal cancer (HNPCC) in which genetic changes within the MSH2 gene are observed in approx. 60% of patients [2,3], gave rise to search for a similar effect on CRC incidence in other types of DNA repair systems. The aim of this study was to investigate the effect of BER gene polymorphisms OGG1 Ser326Cys, XRCC1 Arg399Gln and MUTYH Gln324His on the modulation of CRC risk. [...]these data are supplemented with the levels of 8-oG broken down into each of the tested variants, in order to assess the possible impact of the effectiveness of antioxidant mechanisms on the risk level. [...]measurement of 8-oG levels in relation to specific genotypes showed that group with Ser/Cys genotype of the OGG1 gene had statistically significantly higher level than remaining 2 genotypes. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1232-1087 1896-494X |
DOI: | 10.13075/ijomeh.1896.01901 |