Evidence map›Paper›PMID 25079701›Full record

ArticleGastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association2015

Gene polymorphisms in the ornithine decarboxylase-polyamine pathway modify gastric cancer risk by interaction with isoflavone concentrations.

Lisa Y Cho, Jae Jeong Yang, Kwang-Pil Ko, Seung Hyun Ma, Aesun Shin, Bo Youl Choi, Hyun Ja Kim, Dong Soo Han, Kyu Sang Song, Yong Sung Kim and 5 more

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In one paragraph

Article in Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.3field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 24 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 7 institutions in 2 countries.

Lisa Y ChoDepartment of Preventive Medicine, Seoul National University College of Medicine, 103 Daehakno, Jongno-Gu, Seoul, 110-799, Republic of Korea, lisaycho@snu.ac.kr.
Jae Jeong Yang
Kwang-Pil Ko
Seung Hyun Ma
Aesun Shin
Bo Youl Choi
Hyun Ja Kim
Dong Soo Han
Kyu Sang Song
Yong Sung Kim
Soung-Hoon Chang
Hai-Rim Shin
Daehee Kang
Keun-Young Yoo
Sue K Park
Seoul National University · KRHanyang University · KRNational Cancer Center · KRChungnam National University · KRGachon University · KRKonkuk University · KRKorea Research Institute of Bioscience and Biotechnology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe study aimed to examine the association between genes encoding molecules in the ornithine decarboxylase (ODC)-polyamine pathway (ODC1, AMD1, NQO1, NOS2A, and OAZ2) and gastric cancer risk and whether the gene-phytoestrogen interaction modifies gastric cancer risk.

methodsAmong 76 gastric cancer cases and their 1:4 matched controls within the Korean Multi-center Cancer Cohort, a total of 30 SNPs in five genes involved in the ODC pathway were primarily analyzed. The second-stage genotyping in 388 matched case-control sets was conducted to reevaluate the significant SNPs interacting with phytoestrogens during the primary analysis. The summary odds ratios (ORs) [95 % confidence intervals (CIs)] for gastric cancer were estimated. Interaction effects between the SNPs and plasma concentrations of phytoestrogens (genistein, daidzein, equol, and enterolactone) were evaluated.

resultsIn the pooled analysis, NQO1 rs1800566 showed significant genetic effects on gastric cancer without heterogeneity [OR 0.83 (95 % CI 0.70-0.995)] and a greater decreased risk at high genistein/daidzein levels [OR 0.36 (95 % CI 0.15-0.90) and OR 0.26 (95 % CI 0.10-0.64), respectively; p interaction < 0.05]. Risk alleles of AMD1 rs1279599, AMD1 rs7768897, and OAZ2 rs7403751 had a significant gene-phytoestrogen (genistein and daidzein) interaction effect to modify the development of gastric cancer. They had an increased gastric cancer risk at low isoflavone levels, but a decreased risk at high isoflavone levels (p interaction < 0.01).

conclusionsOur findings suggest that common variants in the genes involved in the ODC pathway may contribute to the risk of gastric cancer possibly by modulating ODC polyamine biosynthesis or by interaction between isoflavones and NQO1, OAZ2, and AMD1.

Indexed as

Polymorphism, Single Nucleotide4-ButyrolactoneAdenosylmethionine DecarboxylaseAsian PeopleCase-Control StudiesEquolGene-Environment InteractionGenisteinHumansIsoflavonesLignansMulticenter Studies as TopicNAD(P)H Dehydrogenase (Quinone)Nitric Oxide Synthase Type IIOrnithine DecarboxylasePhytoestrogens2,3-bis(3'-hydroxybenzyl)butyrolactone4-ButyrolactoneAdenosylmethionine DecarboxylaseAMD1 protein, humandaidzeinEquolGenisteinIsoflavonesLignansNAD(P)H Dehydrogenase (Quinone)Nitric Oxide Synthase Type IINOS2 protein, humanNQO1 protein, humanOrnithine DecarboxylasePhytoestrogensPolyamines

Identifiers

PMID25079701
OpenAlexW2058253257

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.