Login / Signup

Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.

Ben ZhangWei-Hua JiaKoichi MatsudaSun-Seog KweonKeitaro MatsuoYong-Bing XiangAesun ShinSun Ha JeeDong-Hyun KimQiuyin CaiJirong LongJiajun ShiWanqing WenGong YangYanfeng ZhangChun LiBingshan LiYan GuoZefang RenBu-Tian JiZhi-Zhong PanAtsushi TakahashiMin-Ho ShinFumihiko MatsudaYu-Tang GaoJae Hwan OhSoriul KimYoon-Ok Ahnnull nullAndrew T ChanJenny Chang-ClaudeMartha L Slatterynull nullStephen B GruberFredrick R SchumacherStephanie L Stenzelnull nullGraham CaseyHyeong-Rok KimJin-Young JeongJi Won ParkHong-Lan LiSatoyo HosonoSang-Hee ChoMichiaki KuboXiao-Ou ShuYi-Xin ZengWei Zheng
Published in: Nature genetics (2014)
Known genetic loci explain only a small proportion of the familial relative risk of colorectal cancer (CRC). We conducted a genome-wide association study of CRC in East Asians with 14,963 cases and 31,945 controls and identified 6 new loci associated with CRC risk (P = 3.42 × 10(-8) to 9.22 × 10(-21)) at 10q22.3, 10q25.2, 11q12.2, 12p13.31, 17p13.3 and 19q13.2. Two of these loci map to genes (TCF7L2 and TGFB1) with established roles in colorectal tumorigenesis. Four other loci are located in or near genes involved in transcriptional regulation (ZMIZ1), genome maintenance (FEN1), fatty acid metabolism (FADS1 and FADS2), cancer cell motility and metastasis (CD9), and cell growth and differentiation (NXN). We also found suggestive evidence for three additional loci associated with CRC risk near genome-wide significance at 8q24.11, 10q21.1 and 10q24.2. Furthermore, we replicated 22 previously reported CRC-associated loci. Our study provides insights into the genetic basis of CRC and suggests the involvement of new biological pathways.
Keyphrases
  • genome wide
  • genome wide association study
  • dna methylation
  • copy number
  • fatty acid
  • gene expression
  • early onset
  • escherichia coli
  • staphylococcus aureus
  • cystic fibrosis
  • candida albicans