Evidence map›Paper›PMID 29532565›Full record

ArticleCancer science2018

Established gastric cancer cell lines transplantable into C57BL/6 mice show fibroblast growth factor receptor 4 promotion of tumor growth.

Masami Yamamoto, Sachiyo Nomura, Akihiro Hosoi, Koji Nagaoka, Tamaki Iino, Tomohiko Yasuda, Tomoko Saito, Hirokazu Matsushita, Eiji Uchida, Yasuyuki Seto and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

56 citing papers in PubMed, 64 citations in OpenAlex.

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  15. Frizzled-1 amplification promotes fibrosis in the gastric tumor microenvironment through the activation of fibroblasts via the SLIT2/ROBO1 axis.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2026
    Article
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  18. LGMNFrontiers in immunology · 2026
    Article
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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 8 institutions in 2 countries.

Masami YamamotoDepartment of Pathology, Nippon Veterinary and Life Science University, Tokyo, Japan.
Sachiyo NomuraDepartment of Gastrointestinal Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.ORCID http://orcid.org/0000-0003-4293-6205
Akihiro HosoiDepartment of Immunotherapeutics, The University of Tokyo Hospital, Tokyo, Japan.
Koji NagaokaDepartment of Immunotherapeutics, The University of Tokyo Hospital, Tokyo, Japan.
Tamaki IinoDepartment of Immunotherapeutics, The University of Tokyo Hospital, Tokyo, Japan.
Tomohiko YasudaDepartment of Gastrointestinal Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Tomoko SaitoInstitute of Immunology Co., Ltd, Utsunomiya Laboratory, Genetic Modified Animal Group, Utsunomiya, Japan.
Hirokazu MatsushitaDepartment of Immunotherapeutics, The University of Tokyo Hospital, Tokyo, Japan.
Eiji UchidaDepartment of Surgery, Nippon Medical School, Tokyo, Japan.
Yasuyuki SetoDepartment of Gastrointestinal Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
James R GoldenringDepartment of Surgery and the Epithelial Biology Center, Vanderbilt University School of Medicine, Nashville VA Medical Center, Nashville, TN, USA.ORCID http://orcid.org/0000-0002-7833-2940
Kazuhiko KakimiDepartment of Immunotherapeutics, The University of Tokyo Hospital, Tokyo, Japan.ORCID http://orcid.org/0000-0003-2631-3040
Masae TatematsuTatematsu Clinic, Nagoya, Japan.
Tetsuya TsukamotoDepartment of Pathology, Graduate School of Medicine, Fujita Health University, Toyoake, Japan.ORCID http://orcid.org/0000-0002-7502-8724
University of Tokyo Hospital · JPThe University of Tokyo · JPFujita Health University · JPKomatsu (Japan) · JPNippon Medical School · JPNippon Veterinary and Life Science University · JPUtsunomiya University · JPVanderbilt University · US

Funding

Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
NIDDK NIH HHS P30 DK058404
6 · The paper itself

Abstract

Previously no mouse gastric cancer cell lines have been available for transplantation into C57BL/6 mice. However, a gastric cancer model in immunocompetent mice would be useful for analyzing putative therapies. N-Methyl-N-nitrosourea (MNU) was given in drinking water to C57BL/6 mice and p53 heterozygous knockout mice. Only 1 tumor from a p53 knockout mouse could be cultured and the cells s.c. transplanted into a C57BL/6 mouse. We cultured this s.c. tumor, and subcloned it. mRNA expression in the most aggressive YTN16 subline was compared to the less aggressive YTN2 subline by microarray analysis, and fibroblast growth factor receptor 4 (FGFR4) in YTN16 cells was knocked out with a CRISPR/Cas9 system and inhibited by an FGFR4 selective inhibitor, BLU9931. These transplanted cell lines formed s.c. tumors in C57BL/6 mice. Four cell lines (YTN2, YTN3, YTN5, YTN16) were subcloned and established. Their in vitro growth rates were similar. However, s.c. tumor establishment rates, metastatic rates, and peritoneal dissemination rates of YTN2 and YTN3 were lower than for YTN5 and YTN16. YTN16 established 8/8 s.c. tumors, 7/8 with lung metastases, 3/8 with lymph node metastases and 5/5 with peritoneal dissemination. FGFR4 expression by YTN16 was 121-fold higher than YTN2. FGFR4-deleted YTN16 cells failed to form s.c. tumors and showed lower rates of peritoneal dissemination. BLU9931 significantly inhibited the growth of peritoneal dissemination of YTN16. These studies present the first transplantable mouse gastric cancer lines. Our results further indicate that FGFR4 is an important growth signal receptor in gastric cancer cells with high FGFR4 expression.

Indexed as

AnimalsCell Line, TumorCell ProliferationGene Knockout TechniquesImmunocompetenceMethylnitrosoureaMiceMice, Inbred C57BLMice, KnockoutNeoplasm MetastasisNeoplasm TransplantationReceptor, Fibroblast Growth Factor, Type 4Stomach NeoplasmsTumor Suppressor Protein p53Fgfr4 protein, mouseMethylnitrosoureaReceptor, Fibroblast Growth Factor, Type 4Tumor Suppressor Protein p53animal modelC57BL/6 mouseFGFR4gastric cancerimmunocompetent

Identifiers

PMID29532565
PMCPMC5980194
OpenAlexW2793410667

What OpenQuestion holds

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LicenceCC BY-NC
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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.