Department of Gastroenterology, Hospital Clínico Universitario Lozano Blesa, Zaragoza, Spain.
Aragon Health Research Institute (IIS Aragon), Zaragoza, Spain.
Int J Cancer. 2019 Feb 1;144(3):489-502. doi: 10.1002/ijc.31858. Epub 2018 Nov 26.
Our study aimed to evaluate the relevance of genetic susceptibility in the development of colorectal adenomas (CRA) and its relationship with the presence of family history of colorectal cancer (CRC). Genomic DNA from 750 cases (first degree relatives of patients with CRC) and 750 controls (subjects with no family history of CRC) was genotyped for 99 single nucleotide polymorphisms (SNPs) previously associated with CRC/CRA risk by GWAS and candidate gene studies by using the MassArray™ (Sequenom) platform. Cases and controls were matched by gender, age and histological lesion. Eight hundred and fifty-eight patients showed no neoplastic lesions, whereas 288 patients showed low-risk adenomas, and 354 patients presented high-risk adenomas. Two SNPs (rs10505477, rs6983267) in the CASC8 gene were associated with a reduced risk of CRA in controls (log-additive models, OR: 0.67, 95%CI:0.54-0.83, and OR:0.66, 95%CI:0.54-0.84, respectively). Stratified analysis by histological lesion revealed the association of rs10505477 and rs6983267 variants with reduced risk of low- and high-risk adenomas in controls, being this effect stronger in low-risk adenomas (log-additive models, OR:0.63, 95%CI:0.47-0.84 and OR:0.64, 95%CI:0.47-0.86, respectively). Moreover, 2 SNPs (rs10795668, rs11255841) in the noncoding LINC00709 gene were significantly associated with a reduced risk of low-risk adenomas in cases (recessive models, OR:0.22, 95%CI:0.06-0.72, and OR:0.08, 95%CI:0.03-0.61) and controls (dominant models, OR:0.50, 95%CI:0.34-0.75, and OR:0.52, 95%CI:0.35-0.78, respectively). In conclusion, some variants associated with CRC risk (rs10505477, rs6983267, rs10795668 and rs11255841) are also involved in the susceptibility to CRA and specific subtypes. These associations are influenced by the presence of family history of CRC.
我们的研究旨在评估遗传易感性在结直肠腺瘤(CRA)发展中的相关性及其与结直肠癌(CRC)家族史之间的关系。使用 MassArray™(Sequenom)平台,对 750 例病例(CRC 患者的一级亲属)和 750 例对照(无 CRC 家族史的受试者)的基因组 DNA 进行了 99 个单核苷酸多态性(SNP)的基因分型,这些 SNP 先前通过 GWAS 和候选基因研究与 CRC/CRA 风险相关。病例和对照按性别、年龄和组织学病变进行匹配。858 例患者无肿瘤性病变,288 例患者为低危腺瘤,354 例患者为高危腺瘤。CASC8 基因中的 2 个 SNP(rs10505477、rs6983267)与对照中 CRA 风险降低相关(对数相加模型,OR:0.67,95%CI:0.54-0.83,OR:0.66,95%CI:0.54-0.84)。按组织学病变分层分析显示,rs10505477 和 rs6983267 变体与对照中低危和高危腺瘤风险降低相关,这种效应在低危腺瘤中更强(对数相加模型,OR:0.63,95%CI:0.47-0.84 和 OR:0.64,95%CI:0.47-0.86)。此外,非编码 LINC00709 基因中的 2 个 SNP(rs10795668、rs11255841)与病例(隐性模型,OR:0.22,95%CI:0.06-0.72,OR:0.08,95%CI:0.03-0.61)和对照(显性模型,OR:0.50,95%CI:0.34-0.75,OR:0.52,95%CI:0.35-0.78)中低危腺瘤风险降低显著相关。总之,与 CRC 风险相关的一些变体(rs10505477、rs6983267、rs10795668 和 rs11255841)也参与了 CRA 和特定亚型的易感性。这些关联受 CRC 家族史的影响。