{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,12]],"date-time":"2026-06-12T21:24:51Z","timestamp":1781299491417,"version":"3.54.1"},"reference-count":51,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2005,1,28]],"date-time":"2005-01-28T00:00:00Z","timestamp":1106870400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/2.0\/"},{"start":{"date-parts":[[2005,1,28]],"date-time":"2005-01-28T00:00:00Z","timestamp":1106870400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/2.0\/"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["BMC Cancer"],"abstract":"<jats:title>Abstract<\/jats:title><jats:sec>\n                        <jats:title>Background<\/jats:title>\n                        <jats:p>Recent studies relating to the association between DNA repair-gene polymorphisms and colorectal cancer risk would, to the best of our knowledge, appear to be very limited. This study was designed to examine the polymorphisms associated with three DNA repair genes, namely: <jats:italic>XRCC1<\/jats:italic> Arg399Gln, <jats:italic>XRCC3<\/jats:italic> Thr241Met and <jats:italic>XPD<\/jats:italic> Lys751Gln, and investigate their role as susceptibility markers for colorectal cancer.<\/jats:p>\n                     <\/jats:sec><jats:sec>\n                        <jats:title>Methods<\/jats:title>\n                        <jats:p>We conducted a case-control study including 727 cases of cancer and 736 hospital-based age- and sex-matched healthy controls to examine the role of genetic polymorphisms of three DNA-repair genes (<jats:italic>XRCC1<\/jats:italic>, <jats:italic>XRCC3<\/jats:italic> and <jats:italic>XPD<\/jats:italic>) in the context of colorectal cancer risk for the Taiwanese population. Genomic DNA isolated from 10 ml whole blood was used to genotype <jats:italic>XRCC1<\/jats:italic> Arg399Gln, <jats:italic>XRCC3<\/jats:italic> Thr241Met and <jats:italic>XPD<\/jats:italic> Lys751Gln by means of polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) analysis.<\/jats:p>\n                     <\/jats:sec><jats:sec>\n                        <jats:title>Results<\/jats:title>\n                        <jats:p>The risk for colorectal cancer did not appear to differ significantly amongst individuals featuring the <jats:italic>XRCC1<\/jats:italic> 399Arg\/Arg genotype (OR = 1.18; 95% CI, 0.96\u20131.45), the <jats:italic>XRCC3<\/jats:italic> 241Thr\/Thr genotype (OR = 1.25; 95% CI, 0.88\u20131.79) or the <jats:italic>XPD<\/jats:italic> 751Gln allele (OR = 1.20; 95% CI, 0.90\u20131.61), although individuals featuring a greater number of risk genotypes (genotype with OR greater than 1) did experience a higher risk for colorectal cancer when compared to those who didn't feature any risk genotypes (Trend test <jats:italic>P<\/jats:italic> = 0.03). Compared with those individuals who didn't express any putative risk genotypes, individuals featuring all of the putative risk genotypes did experience a significantly greater cancer risk (OR = 2.43, 95% CI = 1.21\u20134.90), particularly for individuals suffering tumors located in the rectum (OR = 3.18, 95% CI = 1.29\u20137.82) and diagnosed prior to the age of 60 years (OR = 4.90, 95% CI = 1.72\u201314.0).<\/jats:p>\n                     <\/jats:sec><jats:sec>\n                        <jats:title>Conclusions<\/jats:title>\n                        <jats:p>Our results suggest that DNA-repair pathways may simultaneously modulate the risk of colorectal cancer for the Taiwanese population, and, particularly for rectal cancer and younger patients.<\/jats:p>\n                     <\/jats:sec>","DOI":"10.1186\/1471-2407-5-12","type":"journal-article","created":{"date-parts":[[2005,1,29]],"date-time":"2005-01-29T08:05:56Z","timestamp":1106985956000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":71,"title":["Polymorphisms of the XRCC1, XRCC3, &amp; XPDgenes, and colorectal cancer risk: a case-control study in Taiwan"],"prefix":"10.1186","volume":"5","author":[{"given":"Chih-Ching","family":"Yeh","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fung-Chang","family":"Sung","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Reiping","family":"Tang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chung Rong","family":"Chang-Chieh","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ling-Ling","family":"Hsieh","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2005,1,28]]},"reference":[{"key":"200_CR1","doi-asserted-by":"crossref","unstructured":"Vineis P: Epidemiology of cancer from exposure to arylamines. 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