Identification of Novel Loci and New Risk Variant in Known Loci for Colorectal Cancer Risk in East Asians.
Adult
Aged
Asian People
/ genetics
Case-Control Studies
China
/ epidemiology
Chromosomes, Human, Pair 1
/ genetics
Colorectal Neoplasms
/ epidemiology
Female
Genetic Loci
Genetic Predisposition to Disease
Genome-Wide Association Study
Humans
INDEL Mutation
Japan
/ epidemiology
Linkage Disequilibrium
Male
Middle Aged
Polymorphism, Single Nucleotide
Republic of Korea
/ epidemiology
Risk Factors
Journal
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
ISSN: 1538-7755
Titre abrégé: Cancer Epidemiol Biomarkers Prev
Pays: United States
ID NLM: 9200608
Informations de publication
Date de publication:
02 2020
02 2020
Historique:
received:
28
06
2019
revised:
30
09
2019
accepted:
04
12
2019
pubmed:
13
12
2019
medline:
20
1
2021
entrez:
13
12
2019
Statut:
ppublish
Résumé
Risk variants identified so far for colorectal cancer explain only a small proportion of familial risk of this cancer, particularly in Asians. We performed a genome-wide association study (GWAS) of colorectal cancer in East Asians, including 23,572 colorectal cancer cases and 48,700 controls. To identify novel risk loci, we selected 60 promising risk variants for replication using data from 58,131 colorectal cancer cases and 67,347 controls of European descent. To identify additional risk variants in known colorectal cancer loci, we performed conditional analyses in East Asians. An indel variant, rs67052019 at 1p13.3, was found to be associated with colorectal cancer risk at In this large GWAS, we identified three novel risk loci and two highly suggestive loci for colorectal cancer risk and provided evidence for potential roles of multiple genes and pathways in the etiology of colorectal cancer. In addition, we showed that additional risk variants exist in many colorectal cancer risk loci identified previously. Our study provides novel data to improve the understanding of the genetic basis for colorectal cancer risk.
Sections du résumé
BACKGROUND
Risk variants identified so far for colorectal cancer explain only a small proportion of familial risk of this cancer, particularly in Asians.
METHODS
We performed a genome-wide association study (GWAS) of colorectal cancer in East Asians, including 23,572 colorectal cancer cases and 48,700 controls. To identify novel risk loci, we selected 60 promising risk variants for replication using data from 58,131 colorectal cancer cases and 67,347 controls of European descent. To identify additional risk variants in known colorectal cancer loci, we performed conditional analyses in East Asians.
RESULTS
An indel variant, rs67052019 at 1p13.3, was found to be associated with colorectal cancer risk at
CONCLUSIONS
In this large GWAS, we identified three novel risk loci and two highly suggestive loci for colorectal cancer risk and provided evidence for potential roles of multiple genes and pathways in the etiology of colorectal cancer. In addition, we showed that additional risk variants exist in many colorectal cancer risk loci identified previously.
IMPACT
Our study provides novel data to improve the understanding of the genetic basis for colorectal cancer risk.
Identifiants
pubmed: 31826910
pii: 1055-9965.EPI-19-0755
doi: 10.1158/1055-9965.EPI-19-0755
pmc: PMC7571256
mid: NIHMS1622552
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, N.I.H., Intramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
477-486Subventions
Organisme : NCI NIH HHS
ID : R01 CA067941
Pays : United States
Organisme : NHGRI NIH HHS
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Organisme : NHGRI NIH HHS
ID : U01 HG004446
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Organisme : NCI NIH HHS
ID : R01 CA042182
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Organisme : NHLBI NIH HHS
ID : HHSN268201100003I
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Informations de copyright
©2019 American Association for Cancer Research.
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