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    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Asian Pacific Journal of Cancer Prevention
    • Volume 17, Issue 6
    • مشاهده مورد
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Asian Pacific Journal of Cancer Prevention
    • Volume 17, Issue 6
    • مشاهده مورد
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    DNMT3B -149 C>T and -579 G>T Polymorphisms and Risk of Gastric and Colorectal Cancer: a Meta-analysis

    (ندگان)پدیدآور
    Khoram-Abadi, KhadijehMirzaee Khoram-Abadi, KhadijehForat-Yazdi, MohammadKheirandish, ShahnazSaeidi, NasimZarezade, ZeinabMehrabi, NahidNeamatzadeh, Hossein
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    نوع مدرک
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    Systematic Review and Meta-analysis
    زبان مدرک
    English
    نمایش کامل رکورد
    چکیده
    Background: Numerous studies have investigated associations of DNA methyltransferase (DNMT) -149 C>T and -579 G>T polymorphisms with gastric cancer (GC) and colorectal cancer (CRC) susceptibility; however, the findings are inconsistent prompting the present meta-analysis. T and -579 G>T polymorphisms with gastric cancer (GC) and colorectal cancer (CRC) susceptibility; however, the findings are inconsistent prompting the present meta-analysis. T polymorphisms with gastric cancer (GC) and colorectal cancer (CRC) susceptibility; however, the findings are inconsistent prompting the present meta-analysis. Materials and Methods: Related studies were identified from PubMed, Google scholar, and SID until 10 October 2015. Pooled odds ratios (ORs) and 95% confidence intervals (CIs) were used to assess the strength of the associations. Results: Eleven studies were included based on the search criteria for CRC and GC related to the DNMT3B 149 C>T (3,353 cases and 4,936 controls) and DNMT3B 579 G>T (1,387 cases and 2,064 controls) polymorphisms. There was no significant association overall between DNMT3B -149 and 579 polymorphisms and the risk of cancer. In the stratified analysis by cancer type, DNMT3B 579G>T polymorphism was associated with the risk of CRC and GC. While the DNMT3B -149C/T polymorphism was related with a significantly increased risk of CRC in two tested models, dominant (GG+GT T (3,353 cases and 4,936 controls) and DNMT3B 579 G>T (1,387 cases and 2,064 controls) polymorphisms. There was no significant association overall between DNMT3B -149 and 579 polymorphisms and the risk of cancer. In the stratified analysis by cancer type, DNMT3B 579G>T polymorphism was associated with the risk of CRC and GC. While the DNMT3B -149C/T polymorphism was related with a significantly increased risk of CRC in two tested models, dominant (GG+GT T (1,387 cases and 2,064 controls) polymorphisms. There was no significant association overall between DNMT3B -149 and 579 polymorphisms and the risk of cancer. In the stratified analysis by cancer type, DNMT3B 579G>T polymorphism was associated with the risk of CRC and GC. While the DNMT3B -149C/T polymorphism was related with a significantly increased risk of CRC in two tested models, dominant (GG+GT T polymorphism was associated with the risk of CRC and GC. While the DNMT3B -149C/T polymorphism was related with a significantly increased risk of CRC in two tested models, dominant (GG+GT vs. TT: OR 0.51, 95 % CI 0.38-0.69; P = 0.00, Pheterogeneity=0.69, I2= 0 %) and heterozygote (GT vs. TT: OR 0.50, 95 % CI 0.37-0.69; P=0.00, Pheterogeneity=0.41, I2= 0 %), no evidence of any association with GC risk was observed as in the pooled analyses. Conclusions: More studies are needed to assess associations of DNMT3B -149C/T and DNMT3B 579G>T polymorphisms with cancer in different ethnicities with large population sizes to generate comprehensive conclusions
    کلید واژگان
    DNA methyltransferases
    CRC
    Gastric cancer
    Polymorphism

    شماره نشریه
    6
    تاریخ نشر
    2016-07-01
    1395-04-11
    ناشر
    West Asia Organization for Cancer Prevention (WAOCP)
    سازمان پدید آورنده
    Department of Anatomy, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
    Department of Anatomy,Shahid Sadoughi University of Medical Sciences, Yazd, Iran
    Department of Internal Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
    Department of Internal Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
    Department of Internal Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
    Department of Internal Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
    Department of Biology, Science Faculty, University of Yazd, Iran
    Department of Medical Genetics, Internationl Campus, Shahid Sadoughi University of Medical Sciences, Yazd, Iran

    شاپا
    1513-7368
    2476-762X
    URI
    https://dx.doi.org/APJCP.2016.17.6.3015
    http://journal.waocp.org/article_16385.html
    https://iranjournals.nlai.ir/handle/123456789/35609

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