A Functional Single Nucleotide Polymorphism in Mucin 1, at Chromosome 1q22, Determines Susceptibility to Diffuse-Type Gastric Cancer

Two major types of gastric cancer, intestinal and diffuse, develop through distinct mechanisms; the diffuse type is considered to be more influenced by genetic factors, although the mechanism is unknown. Our previous genome-wide association study associated 3 single nucleotide polymorphisms (SNPs) w...

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Published inGastroenterology (New York, N.Y. 1943) Vol. 140; no. 3; pp. 892 - 902
Main Authors Saeki, Norihisa, Saito, Akira, Choi, Il Ju, Matsuo, Keitaro, Ohnami, Sumiko, Totsuka, Hirohiko, Chiku, Suenori, Kuchiba, Aya, Lee, Yeon–Su, Yoon, Kyong–Ah, Kook, Myeong–Cherl, Park, Sook Ryun, Kim, Young–Woo, Tanaka, Hideo, Tajima, Kazuo, Hirose, Hiroshi, Tanioka, Fumihiko, Matsuno, Yoshihiro, Sugimura, Haruhiko, Kato, Shunji, Nakamura, Tsuneya, Nishina, Tomohiro, Yasui, Wataru, Aoyagi, Kazuhiko, Sasaki, Hiroki, Yanagihara, Kazuyoshi, Katai, Hitoshi, Shimoda, Tadakazu, Yoshida, Teruhiko, Nakamura, Yusuke, Hirohashi, Setsuo, Sakamoto, Hiromi
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.03.2011
Subjects
Online AccessGet full text
ISSN0016-5085
1528-0012
1528-0012
DOI10.1053/j.gastro.2010.10.058

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Abstract Two major types of gastric cancer, intestinal and diffuse, develop through distinct mechanisms; the diffuse type is considered to be more influenced by genetic factors, although the mechanism is unknown. Our previous genome-wide association study associated 3 single nucleotide polymorphisms (SNPs) with diffuse-type gastric cancer (DGC); 1 was a functional SNP (rs2294008) in prostate stem cell antigen ( PSCA), but the loci of the other 2 were not investigated. We performed high-density mapping to explore a linkage disequilibrium status of the 2 SNPs at chromosome 1q22. A DGC case-control study was conducted using DNA from 606 cases and 1264 controls (all Japanese individuals) and validated using DNA from Japanese (304 cases, 1465 controls) and Korean (452 cases, 372 controls) individuals. The effects of SNPs on function were analyzed by reporter assays and analyses of splice variants. A region of a strong linkage disequilibrium with the 2 SNPs contained mucin 1 ( MUC1) and other 4 genes and SNPs significantly associated with DGC (rs2070803: P = 4.33 × 10 −13; odds ratio [OR], 1.71 by meta-analysis of the studies on the 3 panels) but not with intestinal-type gastric cancer. Functional studies demonstrated that rs4072037 ( P = 1.43 × 10 −11; OR, 1.66 by meta-analysis) in MUC1 affects promoter activity and determines the major splicing variants of MUC1 in the gastric epithelium. Individuals that carry both SNPs rs2294008 in PSCA and rs4072037 in MUC1 have a high risk for developing DGC (OR, 8.38). MUC1 is the second major DGC susceptibility gene identified. The SNPs rs2070803 and rs4072037 in MUC1 might be used to identify individuals at risk for this type of gastric cancer.
AbstractList Two major types of gastric cancer, intestinal and diffuse, develop through distinct mechanisms; the diffuse type is considered to be more influenced by genetic factors, although the mechanism is unknown. Our previous genome-wide association study associated 3 single nucleotide polymorphisms (SNPs) with diffuse-type gastric cancer (DGC); 1 was a functional SNP (rs2294008) in prostate stem cell antigen (PSCA), but the loci of the other 2 were not investigated. We performed high-density mapping to explore a linkage disequilibrium status of the 2 SNPs at chromosome 1q22. A DGC case-control study was conducted using DNA from 606 cases and 1264 controls (all Japanese individuals) and validated using DNA from Japanese (304 cases, 1465 controls) and Korean (452 cases, 372 controls) individuals. The effects of SNPs on function were analyzed by reporter assays and analyses of splice variants. A region of a strong linkage disequilibrium with the 2 SNPs contained mucin 1 (MUC1) and other 4 genes and SNPs significantly associated with DGC (rs2070803: P = 4.33 × 10(-13); odds ratio [OR], 1.71 by meta-analysis of the studies on the 3 panels) but not with intestinal-type gastric cancer. Functional studies demonstrated that rs4072037 (P = 1.43 × 10(-11); OR, 1.66 by meta-analysis) in MUC1 affects promoter activity and determines the major splicing variants of MUC1 in the gastric epithelium. Individuals that carry both SNPs rs2294008 in PSCA and rs4072037 in MUC1 have a high risk for developing DGC (OR, 8.38). MUC1 is the second major DGC susceptibility gene identified. The SNPs rs2070803 and rs4072037 in MUC1 might be used to identify individuals at risk for this type of gastric cancer.
Background & Aims Two major types of gastric cancer, intestinal and diffuse, develop through distinct mechanisms; the diffuse type is considered to be more influenced by genetic factors, although the mechanism is unknown. Our previous genome-wide association study associated 3 single nucleotide polymorphisms (SNPs) with diffuse-type gastric cancer (DGC); 1 was a functional SNP (rs2294008) in prostate stem cell antigen ( PSCA ), but the loci of the other 2 were not investigated. Methods We performed high-density mapping to explore a linkage disequilibrium status of the 2 SNPs at chromosome 1q22. A DGC case-control study was conducted using DNA from 606 cases and 1264 controls (all Japanese individuals) and validated using DNA from Japanese (304 cases, 1465 controls) and Korean (452 cases, 372 controls) individuals. The effects of SNPs on function were analyzed by reporter assays and analyses of splice variants. Results A region of a strong linkage disequilibrium with the 2 SNPs contained mucin 1 ( MUC1 ) and other 4 genes and SNPs significantly associated with DGC (rs2070803: P = 4.33 × 10−13 ; odds ratio [OR], 1.71 by meta-analysis of the studies on the 3 panels) but not with intestinal-type gastric cancer. Functional studies demonstrated that rs4072037 ( P = 1.43 × 10−11 ; OR, 1.66 by meta-analysis) in MUC1 affects promoter activity and determines the major splicing variants of MUC1 in the gastric epithelium. Individuals that carry both SNPs rs2294008 in PSCA and rs4072037 in MUC1 have a high risk for developing DGC (OR, 8.38). Conclusions MUC1 is the second major DGC susceptibility gene identified. The SNPs rs2070803 and rs4072037 in MUC1 might be used to identify individuals at risk for this type of gastric cancer.
Two major types of gastric cancer, intestinal and diffuse, develop through distinct mechanisms; the diffuse type is considered to be more influenced by genetic factors, although the mechanism is unknown. Our previous genome-wide association study associated 3 single nucleotide polymorphisms (SNPs) with diffuse-type gastric cancer (DGC); 1 was a functional SNP (rs2294008) in prostate stem cell antigen ( PSCA), but the loci of the other 2 were not investigated. We performed high-density mapping to explore a linkage disequilibrium status of the 2 SNPs at chromosome 1q22. A DGC case-control study was conducted using DNA from 606 cases and 1264 controls (all Japanese individuals) and validated using DNA from Japanese (304 cases, 1465 controls) and Korean (452 cases, 372 controls) individuals. The effects of SNPs on function were analyzed by reporter assays and analyses of splice variants. A region of a strong linkage disequilibrium with the 2 SNPs contained mucin 1 ( MUC1) and other 4 genes and SNPs significantly associated with DGC (rs2070803: P = 4.33 × 10 −13; odds ratio [OR], 1.71 by meta-analysis of the studies on the 3 panels) but not with intestinal-type gastric cancer. Functional studies demonstrated that rs4072037 ( P = 1.43 × 10 −11; OR, 1.66 by meta-analysis) in MUC1 affects promoter activity and determines the major splicing variants of MUC1 in the gastric epithelium. Individuals that carry both SNPs rs2294008 in PSCA and rs4072037 in MUC1 have a high risk for developing DGC (OR, 8.38). MUC1 is the second major DGC susceptibility gene identified. The SNPs rs2070803 and rs4072037 in MUC1 might be used to identify individuals at risk for this type of gastric cancer.
Two major types of gastric cancer, intestinal and diffuse, develop through distinct mechanisms; the diffuse type is considered to be more influenced by genetic factors, although the mechanism is unknown. Our previous genome-wide association study associated 3 single nucleotide polymorphisms (SNPs) with diffuse-type gastric cancer (DGC); 1 was a functional SNP (rs2294008) in prostate stem cell antigen (PSCA), but the loci of the other 2 were not investigated.BACKGROUND & AIMSTwo major types of gastric cancer, intestinal and diffuse, develop through distinct mechanisms; the diffuse type is considered to be more influenced by genetic factors, although the mechanism is unknown. Our previous genome-wide association study associated 3 single nucleotide polymorphisms (SNPs) with diffuse-type gastric cancer (DGC); 1 was a functional SNP (rs2294008) in prostate stem cell antigen (PSCA), but the loci of the other 2 were not investigated.We performed high-density mapping to explore a linkage disequilibrium status of the 2 SNPs at chromosome 1q22. A DGC case-control study was conducted using DNA from 606 cases and 1264 controls (all Japanese individuals) and validated using DNA from Japanese (304 cases, 1465 controls) and Korean (452 cases, 372 controls) individuals. The effects of SNPs on function were analyzed by reporter assays and analyses of splice variants.METHODSWe performed high-density mapping to explore a linkage disequilibrium status of the 2 SNPs at chromosome 1q22. A DGC case-control study was conducted using DNA from 606 cases and 1264 controls (all Japanese individuals) and validated using DNA from Japanese (304 cases, 1465 controls) and Korean (452 cases, 372 controls) individuals. The effects of SNPs on function were analyzed by reporter assays and analyses of splice variants.A region of a strong linkage disequilibrium with the 2 SNPs contained mucin 1 (MUC1) and other 4 genes and SNPs significantly associated with DGC (rs2070803: P = 4.33 × 10(-13); odds ratio [OR], 1.71 by meta-analysis of the studies on the 3 panels) but not with intestinal-type gastric cancer. Functional studies demonstrated that rs4072037 (P = 1.43 × 10(-11); OR, 1.66 by meta-analysis) in MUC1 affects promoter activity and determines the major splicing variants of MUC1 in the gastric epithelium. Individuals that carry both SNPs rs2294008 in PSCA and rs4072037 in MUC1 have a high risk for developing DGC (OR, 8.38).RESULTSA region of a strong linkage disequilibrium with the 2 SNPs contained mucin 1 (MUC1) and other 4 genes and SNPs significantly associated with DGC (rs2070803: P = 4.33 × 10(-13); odds ratio [OR], 1.71 by meta-analysis of the studies on the 3 panels) but not with intestinal-type gastric cancer. Functional studies demonstrated that rs4072037 (P = 1.43 × 10(-11); OR, 1.66 by meta-analysis) in MUC1 affects promoter activity and determines the major splicing variants of MUC1 in the gastric epithelium. Individuals that carry both SNPs rs2294008 in PSCA and rs4072037 in MUC1 have a high risk for developing DGC (OR, 8.38).MUC1 is the second major DGC susceptibility gene identified. The SNPs rs2070803 and rs4072037 in MUC1 might be used to identify individuals at risk for this type of gastric cancer.CONCLUSIONSMUC1 is the second major DGC susceptibility gene identified. The SNPs rs2070803 and rs4072037 in MUC1 might be used to identify individuals at risk for this type of gastric cancer.
Author Nakamura, Tsuneya
Yanagihara, Kazuyoshi
Kook, Myeong–Cherl
Yoon, Kyong–Ah
Kato, Shunji
Tanioka, Fumihiko
Kim, Young–Woo
Lee, Yeon–Su
Sasaki, Hiroki
Saito, Akira
Sakamoto, Hiromi
Yasui, Wataru
Nakamura, Yusuke
Kuchiba, Aya
Tajima, Kazuo
Matsuno, Yoshihiro
Shimoda, Tadakazu
Park, Sook Ryun
Aoyagi, Kazuhiko
Hirose, Hiroshi
Tanaka, Hideo
Sugimura, Haruhiko
Katai, Hitoshi
Choi, Il Ju
Nishina, Tomohiro
Totsuka, Hirohiko
Hirohashi, Setsuo
Saeki, Norihisa
Yoshida, Teruhiko
Chiku, Suenori
Matsuo, Keitaro
Ohnami, Sumiko
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  organization: Division of Epidemiology and Prevention, Aichi Cancer Center Research Institute, Nagoya, Japan
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  organization: Genetics Division, National Cancer Center Research Institute, Tokyo, Japan
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  organization: Iwata City Hospital, Shizuoka, Japan
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/21070779$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright 2011 AGA Institute
AGA Institute
Copyright © 2011 AGA Institute. Published by Elsevier Inc. All rights reserved.
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– notice: AGA Institute
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1528-0012
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Issue 3
Keywords Stomach Cancer
DGC
Genome-Wide Association Study
GWAS
OR
IGC
PSCA
Risk Genotype
sig
MUC1
por
kb
LD
Cancer Prevention
GC
TR
odds ratio
kilobase
prostate stem cell antigen
diffuse-type gastric cancer
linkage disequilibrium
signet-ring cell carcinoma
poorly differentiated adenocarcinoma
mucin 1
gastric cancer
tandem repeats
intestinal-type gastric cancer
Language English
License Copyright © 2011 AGA Institute. Published by Elsevier Inc. All rights reserved.
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PublicationTitle Gastroenterology (New York, N.Y. 1943)
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Snippet Two major types of gastric cancer, intestinal and diffuse, develop through distinct mechanisms; the diffuse type is considered to be more influenced by genetic...
Background & Aims Two major types of gastric cancer, intestinal and diffuse, develop through distinct mechanisms; the diffuse type is considered to be more...
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SubjectTerms Asian Continental Ancestry Group - genetics
Cancer Prevention
Case-Control Studies
Cell Line, Tumor
Chromosomes, Human, Pair 1
Exons
Female
Gastroenterology and Hepatology
Genetic Predisposition to Disease
Genome-Wide Association Study
Haplotypes
Humans
Japan - epidemiology
Linkage Disequilibrium
Logistic Models
Male
Middle Aged
Mucin-1 - genetics
Mucin-1 - metabolism
Odds Ratio
Phenotype
Polymorphism, Single Nucleotide
Promoter Regions, Genetic
Republic of Korea - epidemiology
Risk Assessment
Risk Factors
Risk Genotype
Stomach Cancer
Stomach Neoplasms - ethnology
Stomach Neoplasms - genetics
Stomach Neoplasms - pathology
Transfection
Title A Functional Single Nucleotide Polymorphism in Mucin 1, at Chromosome 1q22, Determines Susceptibility to Diffuse-Type Gastric Cancer
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https://www.clinicalkey.es/playcontent/1-s2.0-S0016508510016057
https://dx.doi.org/10.1053/j.gastro.2010.10.058
https://www.ncbi.nlm.nih.gov/pubmed/21070779
https://www.proquest.com/docview/855910664
Volume 140
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