Evidence map›Paper›PMID 29976636›Full record

ArticleCancer genomics & proteomics

Overexpression of

Dai Shimizu, Tomoko Saito, Shuhei Ito, Takaaki Masuda, Junji Kurashige, Yosuke Kuroda, Hidetoshi Eguchi, Yasuhiro Kodera, Koshi Mimori

Open access · diamondAbstract read
In one paragraph

Article in Cancer genomics & proteomics. 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
0.7field-weighted citation impact, top 30% 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, 18 citations in OpenAlex.

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  4. A novel small molecule RK-019 inhibitsFrontiers in pharmacology · 2022
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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

9 authors at 3 institutions in 1 country.

Dai ShimizuDepartment of Surgery, Kyushu University Beppu Hospital, Tsurumihara, Japan.
Tomoko SaitoDepartment of Surgery, Kyushu University Beppu Hospital, Tsurumihara, Japan.
Shuhei ItoDepartment of Surgery, Kyushu University Beppu Hospital, Tsurumihara, Japan.
Takaaki MasudaDepartment of Surgery, Kyushu University Beppu Hospital, Tsurumihara, Japan.
Junji KurashigeDepartment of Surgery, Kyushu University Beppu Hospital, Tsurumihara, Japan.
Yosuke KurodaDepartment of Surgery, Kyushu University Beppu Hospital, Tsurumihara, Japan.
Hidetoshi EguchiDepartment of Surgery, Kyushu University Beppu Hospital, Tsurumihara, Japan.
Yasuhiro KoderaDepartment of Gastroenterological Surgery (Surgery II), Nagoya University Graduate School of Medicine, Nagoya, Japan.
Koshi MimoriDepartment of Surgery, Kyushu University Beppu Hospital, Tsurumihara, Japan kmimori@beppu.kyushu-u.ac.jp.
Kyushu University Beppu Hospital · JPNagoya University · JPKumamoto Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeritoneal dissemination (PD) is one of the most common causes of cancer-related mortality in gastric cancer (GC). We aimed to identify PD-associated genes and investigate their role in GC. MATERIALS AND

methodsWe identified FGFR1 as a putative PD-associated gene using a bioinformatics approach. The biological significance of FGFR1 in epithelial-to-mesenchymal transition (EMT) was evaluated according to the correlation with genes that participated in EMT and FGFR1 knockdown experiments. The associations between FGFR1 expression and the clinicopathological features were examined.

resultsFGFR1 expression positively correlated with SNAI1, VIM and ZEB1 expression, and negatively correlated with CDH1 expression. Knockdown of FGFR1 suppressed the malignant phenotype of GC cells. High FGFR1 expression significantly correlated with the peritoneal lavage cytology and synchronous PD positivity as well as poor prognosis.

conclusionHigh FGFR1 expression was associated with PD via promotion of EMT and led to a poor prognosis of GC patients.

Indexed as

Cell MovementEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticAgedApoptosisBiomarkers, TumorCell ProliferationFemaleHumansMaleNeoplasm InvasivenessPeritoneal NeoplasmsPrognosisReceptor, Fibroblast Growth Factor, Type 1Stomach NeoplasmsSurvival RateBiomarkers, TumorFGFR1 protein, humanReceptor, Fibroblast Growth Factor, Type 1epithelial to mesenchymal transitionFGFR1Gastric cancerperitoneal dissemination

Identifiers

PMID29976636
PMCPMC6070707
OpenAlexW2830238625

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.