論文

査読有り 国際誌
2022年8月16日

SNP rs2920280 in PSCA Is Associated with Susceptibility to Gastric Mucosal Atrophy and Is a Promising Biomarker in Japanese Individuals with Helicobacter pylori Infection

Diagnostics
  • Hajime Isomoto
  • Takuki Sakaguchi
  • Tatsuo Inamine
  • Shintaro Takeshita
  • Daisuke Fukuda
  • Ken Ohnita
  • Tsutomu Kanda
  • Kayoko Matsushima
  • Tetsuro Honda
  • Takaaki Sugihara
  • Tatsuro Hirayama
  • Kazuhiko Nakao
  • Kazuhiro Tsukamoto
  • 全て表示

12
8
開始ページ
1988
終了ページ
1988
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.3390/diagnostics12081988
出版者・発行元
MDPI AG

Helicobacter pylori infection results in gastric cancer (GC) with gastric mucosal atrophy (GMA). Some single-nucleotide polymorphisms (SNPs) in the prostate stem cell antigen gene (PSCA) are associated with GC and duodenal ulcers. However, the relationship of other identified SNPs in PSCA with these diseases remains unclear. Herein, the association between PSCA SNPs and GMA among 195 Japanese individuals with H. pylori infection was evaluated. The definition of GMA or non-GMA was based on serum pepsinogen levels or endoscopic findings. Five tag PSCA SNPs were analyzed using PCR high-resolution melting curve analysis with nonlabelled probes. The frequencies of alleles and the genotypes of each tag SNP were compared between the GMA and non-GMA groups. Subsequently, a genetic test was performed using associated SNPs as biomarkers to detect patients developing GMA. Two tag PSCA SNPs (rs2920280 and rs2294008) were related to GMA susceptibility. Individuals with the rs2920280 G/G genotype or the rs2294008 T/T genotype in PSCA had 3.5- and 2.1-fold susceptibility to GMA, respectively. In conclusion, SNP rs2920280 is a possible biomarker for detecting individuals developing GMA. PSCA polymorphisms may be useful biomarkers for predicting GMA linked to GC risk and a screening endoscopy strategy to detect GC related to early stage H. pylori associated GMA.

リンク情報
DOI
https://doi.org/10.3390/diagnostics12081988
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/36010338
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407312
URL
https://www.mdpi.com/2075-4418/12/8/1988/pdf
ID情報
  • DOI : 10.3390/diagnostics12081988
  • eISSN : 2075-4418
  • PubMed ID : 36010338
  • PubMed Central 記事ID : PMC9407312

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