Evidence map›Paper›PMID 23551873›Full record

ArticleCancer science2013

Novel mouse model for Gardner syndrome generated by a large-scale N-ethyl-N-nitrosourea mutagenesis program.

Hideaki Toki, Maki Inoue, Hiromi Motegi, Osamu Minowa, Hiroaki Kanda, Noriko Yamamoto, Ami Ikeda, Yuko Karashima, Junko Matsui, Hideki Kaneda and 9 more

Open access · greenAbstract read
In one paragraph

Article in Cancer science, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed, 9 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

19 authors at 4 institutions in 2 countries.

Hideaki TokiTeam for Advanced Development and Evaluation of Human Disease Models, Riken BioResource Center, Tsukuba, Japan.
Maki Inoue
Hiromi Motegi
Osamu Minowa
Hiroaki Kanda
Noriko Yamamoto
Ami Ikeda
Yuko Karashima
Junko Matsui
Hideki Kaneda
Ikuo Miura
Tomohiro Suzuki
Shigeharu Wakana
Hiroshi Masuya
Yoichi Gondo
Toshihiko Shiroishi
Tetsu Akiyama
Ryoji Yao
Tetsuo Noda
RIKEN BioResource Research Center · JPJapanese Foundation For Cancer Research · JPDivision of Molecular & Cellular Biosciences · USNational Institute of Genetics · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutant mouse models are indispensable tools for clarifying the functions of genes and elucidating the underlying pathogenic mechanisms of human diseases. We carried out large-scale mutagenesis using the chemical mutagen N-ethyl-N-nitrosourea. One specific aim of our mutagenesis project was to generate novel cancer models. We screened 7012 animals for dominant traits using a necropsy test and thereby established 17 mutant lines predisposed to cancer. Here, we report on a novel cancer model line that developed osteoma, trichogenic tumor, and breast cancer. Using fine mapping and genomic sequencing, we identified a point mutation in the adenomatous polyposis coli (Apc) gene. The Apc1576 mutants bear a nonsense mutation at codon 1576 in the Apc gene. Although most Apc mutant mice established thus far have multifocal intestinal tumors, mice that are heterozygous for the Apc1576 mutation do not develop intestinal tumors; instead, they develop multifocal breast cancers and trichogenic tumors. Notably, the osteomas that develop in the Apc1576 mutant mice recapitulate the lesion observed in Gardner syndrome, a clinical variant of familial adenomatous polyposis. Our Apc1576 mutant mice will be valuable not only for understanding the function of the Apc gene in detail but also as models of human Gardner syndrome.

Indexed as

Disease Models, AnimalEthylnitrosoureaMutagensAnimalsCodonFemaleGardner SyndromeGenes, APCGenomeHeterozygoteIntestinal NeoplasmsMaleMammary Neoplasms, ExperimentalMiceMutagenesisMutationCodonEthylnitrosoureaMutagens

Identifiers

PMID23551873
PMCPMC7657124
OpenAlexW2061681236

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.