Two variants on T2DM susceptible gene HHEX are associated with CRC risk in a Chinese population

• Published in: Oncotarget Vol. 7; no. 20; pp. 29770 - 29779
• Main Authors: Sun, Rui, Liu, Jian-Ping, Gao, Chang, Xiong, Ying-Ying, Li, Min, Wang, Ya-Ping, Su, Yan-Wei, Lin, Mei, Jiang, An-Li, Xiong, Ling-Fan, Xie, Yan, Feng, Jue-Ping
• Format: Journal Article
• Language: English
• Published: United States Impact Journals LLC 17.05.2016
• Subjects: Asian Continental Ancestry Group - genetics; Colorectal Neoplasms - genetics; Diabetes Mellitus, Type 2 - complications; Diabetes Mellitus, Type 2 - genetics; Female; Genetic Predisposition to Disease - genetics; Genotype; Homeodomain Proteins - genetics; Humans; Male; Middle Aged; Polymorphism, Single Nucleotide; Research Paper; Risk Factors; Transcription Factors - genetics; genetic variants; type 2 diabetes mellitus; HHEX; colorectal cancer
• DOI: 10.18632/oncotarget.8865
• ISSN: 1949-2553

Increasing amounts of evidence has demonstrated that T2DM (Type 2 Diabetes Mellitus) patients have increased susceptibility to CRC (colorectal cancer). As HHEX is a recognized susceptibility gene in T2DM, this work was focused on two SNPs in HHEX, rs1111875 and rs7923837, to study their association with CRC. T2DM patients without CRC (T2DM-only, n=300), T2DM with CRC (T2DM/CRC, n=135), cancer-free controls (Control, n=570), and CRC without T2DM (CRC-only, n=642) cases were enrolled. DNA samples were extracted from the peripheral blood leukocytes of the patients and sequenced by direct sequencing. The χ2 test was used to compare categorical data. We found that in T2DM patients, rs1111875 but not the rs7923837 in HHEX gene was associated with the occurrence of CRC (p= 0.006). for rs1111875, TC/CC patients had an increased risk of CRC (p=0.019, OR=1.592, 95%CI=1.046-2.423). Moreover, our results also indicated that the two variants of HEEX gene could be risk factors for CRC in general population, independent on T2DM (p< 0.001 for rs1111875, p=0.001 for rs7923837). For rs1111875, increased risk of CRC was observed in TC or TC/CC than CC individuals (p<0.001, OR= 1.780, 95%CI= 1.385-2.287; p<0.001, OR= 1.695, 95%CI= 1.335-2.152). For rs7923837, increased CRC risk was observed in AG, GG, and AG/GG than AA individuals (p< 0.001, OR= 1.520, 95%CI= 1.200-1.924; p=0.036, OR= 1.739, 95%CI= 0.989-3.058; p< 0.001, OR= 1.540, 95%CI= 1.225-1.936). This finding highlights the potentially functional alteration with HHEX rs1111875 and rs7923837 polymorphisms may increase CRC susceptibility. Risk effects and the functional impact of these polymorphisms need further validation.