Evidence map›Paper›PMID 23899160›Full record

ArticleBMC gastroenterology2013

Gene expression analysis of a Helicobacter pylori-infected and high-salt diet-treated mouse gastric tumor model: identification of CD177 as a novel prognostic factor in patients with gastric cancer.

Takeshi Toyoda, Tetsuya Tsukamoto, Masami Yamamoto, Hisayo Ban, Noriko Saito, Shinji Takasu, Liang Shi, Ayumi Saito, Seiji Ito, Yoshitaka Yamamura and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC gastroenterology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

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  15. Animal Models andJournal of clinical medicine · 2022
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  20. Genome-wide transcriptional analysis ofPharmaceutical biology · 2020
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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

14 authors at 7 institutions in 1 country.

Takeshi Toyoda
Tetsuya Tsukamoto
Masami Yamamoto
Hisayo Ban
Noriko Saito
Shinji Takasu
Liang Shi
Ayumi Saito
Seiji Ito
Yoshitaka Yamamura
Akiyoshi Nishikawa
Kumiko Ogawa
Takuji Tanaka
Masae Tatematsu
Aichi Cancer Center · JPNational Institute of Health Sciences · JPFujita Health University · JPMie University · JPMitsui Chemicals (Japan) · JPNippon Veterinary and Life Science University · JPOkazaki Institute for Integrative Bioscience · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHelicobacter pylori (H. pylori) infection and excessive salt intake are known as important risk factors for stomach cancer in humans. However, interactions of these two factors with gene expression profiles during gastric carcinogenesis remain unclear. In the present study, we investigated the global gene expression associated with stomach carcinogenesis and prognosis of human gastric cancer using a mouse model.

methodsTo find candidate genes involved in stomach carcinogenesis, we firstly constructed a carcinogen-induced mouse gastric tumor model combined with H. pylori infection and high-salt diet. C57BL/6J mice were given N-methyl-N-nitrosourea in their drinking water and sacrificed after 40 weeks. Animals of a combination group were inoculated with H. pylori and fed a high-salt diet. Gene expression profiles in glandular stomach of the mice were investigated by oligonucleotide microarray. Second, we examined an availability of the candidate gene as prognostic factor for human patients. Immunohistochemical analysis of CD177, one of the up-regulated genes, was performed in human advanced gastric cancer specimens to evaluate the association with prognosis.

resultsThe multiplicity of gastric tumor in carcinogen-treated mice was significantly increased by combination of H. pylori infection and high-salt diet. In the microarray analysis, 35 and 31 more than two-fold up-regulated and down-regulated genes, respectively, were detected in the H. pylori-infection and high-salt diet combined group compared with the other groups. Quantitative RT-PCR confirmed significant over-expression of two candidate genes including Cd177 and Reg3g. On immunohistochemical analysis of CD177 in human advanced gastric cancer specimens, over-expression was evident in 33 (60.0%) of 55 cases, significantly correlating with a favorable prognosis (P = 0.0294). Multivariate analysis including clinicopathological factors as covariates revealed high expression of CD177 to be an independent prognostic factor for overall survival.

conclusionsThese results suggest that our mouse model combined with H. pylori infection and high-salt diet is useful for gene expression profiling in gastric carcinogenesis, providing evidence that CD177 is a novel prognostic factor for stomach cancer. This is the first report showing a prognostic correlation between CD177 expression and solid tumor behavior.

Indexed as

Disease Models, AnimalGene Expression Regulation, NeoplasticHelicobacter pyloriAnimalsGastric MucosaGene Expression ProfilingGPI-Linked ProteinsHelicobacter InfectionsHumansImmunohistochemistryIsoantigensMaleMice, Inbred C57BLMiddle AgedOligonucleotide Array Sequence AnalysisPancreatitis-Associated ProteinsCD177 protein, humanGPI-Linked ProteinsIsoantigensPancreatitis-Associated ProteinsProteinsReceptors, Cell SurfaceREG3G protein, humanSodium, Dietary

Identifiers

PMID23899160
PMCPMC3734037
OpenAlexW2155089326

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LicenceCC BY
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Registered trials

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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.