TY - JOUR
T1 - Association between cyclin D1 polymorphism with CpG island promoter methylation status of tumor suppressor genes in gastric cancer
AU - Tahara, Tomomitsu
AU - Shibata, Tomoyuki
AU - Nakamura, Masakatsu
AU - Yamashita, Hiromi
AU - Yoshioka, Daisuke
AU - Okubo, Masaaki
AU - Yonemura, Joh
AU - Maeda, Yoshiteru
AU - Maruyama, Naoko
AU - Kamano, Toshiaki
AU - Kamiya, Yoshio
AU - Fujita, Hiroshi
AU - Nakagawa, Yoshihito
AU - Nagasaka, Mitsuo
AU - Iwata, Masami
AU - Hirata, Ichiro
AU - Arisawa, Tomiyasu
N1 - Copyright:
Copyright 2011 Elsevier B.V., All rights reserved.
PY - 2010/12
Y1 - 2010/12
N2 - Background: CpG island hypermethylation of tumor suppressor genes is highly involved in gastric carcinogenesis, and enhanced cell proliferation could accelerate this process. Cyclin D1 regulates cell cycle function and may play a role in methylation-related carcinogenesis. Aims: We investigated the association between Cyclin D1 gene G870A polymorphism and the methylation status of tumor suppressor genes in gastric cancer. Methods: Polymorphisms at G870A in the Cyclin D1 gene were genotyped, and methylation status of the p14, p16, DAP-kinase, and CDH1 genes were determined by methylation-specific-polymerase chain reaction in 139 gastric cancer tissues. CIHM high was defined as three or more methylated CpG islands. Results: Although no association was found between methylation status and different stages and Lauren's subtypes, patients with CIHM of DAP-kinase showed significantly worse survival than those without (p = 0.017). In addition, the number of methylated sites was also associated with survival curves (p = 0.0397). The 870G carrier a significantly lower prevalence of CIHM high compared to the AA genotype in advanced-stage gastric cancer (adjusted OR = 0.32, p = 0.047). A weak correlation between the same genotypes and CIHM of p14 were found in the same subtype (adjusted OR = 0.32, p = 0.052). The mean methylation number was significantly lower in G carriers than in AA genotypes in advanced-stage gastric cancer (p = 0.017). Conclusions: Genetic polymorphism of CCND1 is associated with CIHM status in gastric cancer, especially in the advanced stage, but is independent of clinico-pathological features.
AB - Background: CpG island hypermethylation of tumor suppressor genes is highly involved in gastric carcinogenesis, and enhanced cell proliferation could accelerate this process. Cyclin D1 regulates cell cycle function and may play a role in methylation-related carcinogenesis. Aims: We investigated the association between Cyclin D1 gene G870A polymorphism and the methylation status of tumor suppressor genes in gastric cancer. Methods: Polymorphisms at G870A in the Cyclin D1 gene were genotyped, and methylation status of the p14, p16, DAP-kinase, and CDH1 genes were determined by methylation-specific-polymerase chain reaction in 139 gastric cancer tissues. CIHM high was defined as three or more methylated CpG islands. Results: Although no association was found between methylation status and different stages and Lauren's subtypes, patients with CIHM of DAP-kinase showed significantly worse survival than those without (p = 0.017). In addition, the number of methylated sites was also associated with survival curves (p = 0.0397). The 870G carrier a significantly lower prevalence of CIHM high compared to the AA genotype in advanced-stage gastric cancer (adjusted OR = 0.32, p = 0.047). A weak correlation between the same genotypes and CIHM of p14 were found in the same subtype (adjusted OR = 0.32, p = 0.052). The mean methylation number was significantly lower in G carriers than in AA genotypes in advanced-stage gastric cancer (p = 0.017). Conclusions: Genetic polymorphism of CCND1 is associated with CIHM status in gastric cancer, especially in the advanced stage, but is independent of clinico-pathological features.
UR - http://www.scopus.com/inward/record.url?scp=78649316677&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=78649316677&partnerID=8YFLogxK
U2 - 10.1007/s10620-010-1206-5
DO - 10.1007/s10620-010-1206-5
M3 - Article
C2 - 20397048
AN - SCOPUS:78649316677
SN - 0163-2116
VL - 55
SP - 3449
EP - 3457
JO - Digestive Diseases and Sciences
JF - Digestive Diseases and Sciences
IS - 12
ER -