Association between cyclin D1 (CCND1) polymorphism and gastric cancer risk in Japanese population

Tomomitsu Tahara, Tomiyasu Arisawa, Tomoyuki Shibata, Hiromi Yamashita, Ichiro Hirata

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Background/Aims: A complex interaction of genetic and environmental factors is relevant in gastric carcinogenesis. Cyclin D1 (CCND1) is known to regulate function in G1 arrest and therefore, may play an important role in carcinogenesis. The present study aimed to clarify the effect of G870A polymorphism of the CCND1 gene on the risk of gastric cancer (GC) in a Japanese population. Methodology: Restriction fragment length polymorphism analysis was performed for polymorphisms at 870GA in the CCND1 gene in 392 GC and 359 cancer-free subjects including 203 H. pylori positive gastritis and 156 H. pylori negative healthy stomach Results: Non significant association was found between CCND1 G870A genotypes and risk of GC when compared to that of all non-cancer subjects (AA vs. GG+GA: OR=1.13, 95%CI=0.81-1.58, A carrier vs. GG: OR=1.13, 95%CI=0.81-1.56), healthy stomach(AA vs. GG+GA: OR=1.27, 95%CI=0.81-2.00, A carrier vs. GG: OR=1.13, 95%CI=0.8-1.84) and gastritis. (AA vs. GG+GA: OR=1.03, 95%CI=0.7-1.53, p=0.92, A carrier vs. GG: 1.06, 95%CI=0.72-1.56, p=0.77)No association was found between CCND1 genotypes and any of clinico-pathological features of GC. Conclusion: It appears that the G870 polymorphism of CCND1 is not associated with the risk of GC in the Japanese population.

Original languageEnglish
Pages (from-to)1232-1235
Number of pages4
JournalHepato-Gastroenterology
Volume56
Issue number93
Publication statusPublished - 01-07-2009

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Cyclin D1
Stomach Neoplasms
bcl-1 Genes
Stomach
Population
Pylorus
Gastritis
Carcinogenesis
Genotype
Restriction Fragment Length Polymorphisms
Neoplasms

All Science Journal Classification (ASJC) codes

  • Gastroenterology
  • Hepatology

Cite this

Tahara, T., Arisawa, T., Shibata, T., Yamashita, H., & Hirata, I. (2009). Association between cyclin D1 (CCND1) polymorphism and gastric cancer risk in Japanese population. Hepato-Gastroenterology, 56(93), 1232-1235.
Tahara, Tomomitsu ; Arisawa, Tomiyasu ; Shibata, Tomoyuki ; Yamashita, Hiromi ; Hirata, Ichiro. / Association between cyclin D1 (CCND1) polymorphism and gastric cancer risk in Japanese population. In: Hepato-Gastroenterology. 2009 ; Vol. 56, No. 93. pp. 1232-1235.
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abstract = "Background/Aims: A complex interaction of genetic and environmental factors is relevant in gastric carcinogenesis. Cyclin D1 (CCND1) is known to regulate function in G1 arrest and therefore, may play an important role in carcinogenesis. The present study aimed to clarify the effect of G870A polymorphism of the CCND1 gene on the risk of gastric cancer (GC) in a Japanese population. Methodology: Restriction fragment length polymorphism analysis was performed for polymorphisms at 870GA in the CCND1 gene in 392 GC and 359 cancer-free subjects including 203 H. pylori positive gastritis and 156 H. pylori negative healthy stomach Results: Non significant association was found between CCND1 G870A genotypes and risk of GC when compared to that of all non-cancer subjects (AA vs. GG+GA: OR=1.13, 95{\%}CI=0.81-1.58, A carrier vs. GG: OR=1.13, 95{\%}CI=0.81-1.56), healthy stomach(AA vs. GG+GA: OR=1.27, 95{\%}CI=0.81-2.00, A carrier vs. GG: OR=1.13, 95{\%}CI=0.8-1.84) and gastritis. (AA vs. GG+GA: OR=1.03, 95{\%}CI=0.7-1.53, p=0.92, A carrier vs. GG: 1.06, 95{\%}CI=0.72-1.56, p=0.77)No association was found between CCND1 genotypes and any of clinico-pathological features of GC. Conclusion: It appears that the G870 polymorphism of CCND1 is not associated with the risk of GC in the Japanese population.",
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Tahara, T, Arisawa, T, Shibata, T, Yamashita, H & Hirata, I 2009, 'Association between cyclin D1 (CCND1) polymorphism and gastric cancer risk in Japanese population', Hepato-Gastroenterology, vol. 56, no. 93, pp. 1232-1235.

Association between cyclin D1 (CCND1) polymorphism and gastric cancer risk in Japanese population. / Tahara, Tomomitsu; Arisawa, Tomiyasu; Shibata, Tomoyuki; Yamashita, Hiromi; Hirata, Ichiro.

In: Hepato-Gastroenterology, Vol. 56, No. 93, 01.07.2009, p. 1232-1235.

Research output: Contribution to journalArticle

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T1 - Association between cyclin D1 (CCND1) polymorphism and gastric cancer risk in Japanese population

AU - Tahara, Tomomitsu

AU - Arisawa, Tomiyasu

AU - Shibata, Tomoyuki

AU - Yamashita, Hiromi

AU - Hirata, Ichiro

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N2 - Background/Aims: A complex interaction of genetic and environmental factors is relevant in gastric carcinogenesis. Cyclin D1 (CCND1) is known to regulate function in G1 arrest and therefore, may play an important role in carcinogenesis. The present study aimed to clarify the effect of G870A polymorphism of the CCND1 gene on the risk of gastric cancer (GC) in a Japanese population. Methodology: Restriction fragment length polymorphism analysis was performed for polymorphisms at 870GA in the CCND1 gene in 392 GC and 359 cancer-free subjects including 203 H. pylori positive gastritis and 156 H. pylori negative healthy stomach Results: Non significant association was found between CCND1 G870A genotypes and risk of GC when compared to that of all non-cancer subjects (AA vs. GG+GA: OR=1.13, 95%CI=0.81-1.58, A carrier vs. GG: OR=1.13, 95%CI=0.81-1.56), healthy stomach(AA vs. GG+GA: OR=1.27, 95%CI=0.81-2.00, A carrier vs. GG: OR=1.13, 95%CI=0.8-1.84) and gastritis. (AA vs. GG+GA: OR=1.03, 95%CI=0.7-1.53, p=0.92, A carrier vs. GG: 1.06, 95%CI=0.72-1.56, p=0.77)No association was found between CCND1 genotypes and any of clinico-pathological features of GC. Conclusion: It appears that the G870 polymorphism of CCND1 is not associated with the risk of GC in the Japanese population.

AB - Background/Aims: A complex interaction of genetic and environmental factors is relevant in gastric carcinogenesis. Cyclin D1 (CCND1) is known to regulate function in G1 arrest and therefore, may play an important role in carcinogenesis. The present study aimed to clarify the effect of G870A polymorphism of the CCND1 gene on the risk of gastric cancer (GC) in a Japanese population. Methodology: Restriction fragment length polymorphism analysis was performed for polymorphisms at 870GA in the CCND1 gene in 392 GC and 359 cancer-free subjects including 203 H. pylori positive gastritis and 156 H. pylori negative healthy stomach Results: Non significant association was found between CCND1 G870A genotypes and risk of GC when compared to that of all non-cancer subjects (AA vs. GG+GA: OR=1.13, 95%CI=0.81-1.58, A carrier vs. GG: OR=1.13, 95%CI=0.81-1.56), healthy stomach(AA vs. GG+GA: OR=1.27, 95%CI=0.81-2.00, A carrier vs. GG: OR=1.13, 95%CI=0.8-1.84) and gastritis. (AA vs. GG+GA: OR=1.03, 95%CI=0.7-1.53, p=0.92, A carrier vs. GG: 1.06, 95%CI=0.72-1.56, p=0.77)No association was found between CCND1 genotypes and any of clinico-pathological features of GC. Conclusion: It appears that the G870 polymorphism of CCND1 is not associated with the risk of GC in the Japanese population.

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