Evidence map›Paper›PMID 17598916›Full record

ArticleBMC genetics2007

New chemically induced skin tumour susceptibility loci identified in a mouse backcross between FVB and dominant resistant PWK.

Kyoko Fujiwara, Jun Igarashi, Natsumi Irahara, Makoto Kimura, Hiroki Nagase

Open access · diamondAbstract read
In one paragraph

Article in BMC genetics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

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  7. Variants in an Hdac9 intronic enhancer plasmid impact Twist1 expression in vitro.Mammalian genome : official journal of the International Mammalian Genome Society · 2016
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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

5 authors at 2 institutions in 2 countries.

Kyoko FujiwaraDepartment of Cancer Genetics, Roswell Park Cancer Institute, Buffalo, New York 14263, USA. kyoko.fujiwara@roswellpark.org <kyoko.fujiwara@roswellpark.org>
Jun Igarashi
Natsumi Irahara
Makoto Kimura
Hiroki Nagase
Cancer Genetics (United States) · USNihon University · JP

Funding

Analysis and Identification of Skin Cancer in MiceR01ES012249 · NIEHS · ROSWELL PARK CANCER INSTITUTE CORP · PI NAGASE, HIROKI · 2004 to 2008
$2.0M
NCI NIH HHS CA016156NIEHS NIH HHS ES012249-01NIEHS NIH HHS R01 ES012249
6 · The paper itself

Abstract

backgroundA variety of skin cancer susceptibility among mouse strains has allowed identification of genes responsible for skin cancer development. Fifteen Skts loci for skin tumour susceptibility have been mapped so far by using the two-stage skin carcinogenesis model [induced by 7.12-dimethylbenz(a)anthracene (DMBA)/12-O-tetradecanoylphorbol-13-acetate (TPA)]. A few responsible genes have been identified using wild-derived dominant resistant Mus spretus mice, and one has been confirmed as a low penetrance cancer susceptibility gene in a variety of human cancers.

resultsIn the present study, we found that wild-derived PWK mice developed no tumour by treatment with the two-stage skin carcinogenesis protocol. This phenotype is dominant resistant when crossed with the highly susceptible strain FVB. By analyzing the F1 backcross generation between PWK and FVB, we found empirical evidence of significant linkage at the new loci Skts-fp1 on chromosome 4 and suggestive linkage on chromosomes 1, 3, 11, 12 and 14 for skin tumour susceptibility. Skts-fp1 includes the Skts7 interval, which was previously mapped by a Mus spretus and NIH backcross. We also observed suggestive linkage on chromosomes 1 and 2 in the female population only, while suggestive linkage on chromosomes 14 and 15 only was observed in the male population. A significant genetic interaction was seen between markers of D11Mit339 and D16Mit14.

conclusionAnalysis of this new cross may facilitate the identification of genes responsible for mouse skin cancer susceptibility and may reveal their biological interactions.

Indexed as

9,10-Dimethyl-1,2-benzanthraceneGenetic Predisposition to DiseaseTetradecanoylphorbol AcetateAnimalsChromosome MappingCrosses, GeneticDrug ResistanceFemaleGenes, DominantGenetic LinkageGenotypeMaleMiceMice, Inbred StrainsNeoplasms, Second PrimaryPapilloma9,10-Dimethyl-1,2-benzanthraceneTetradecanoylphorbol Acetate

Identifiers

PMID17598916
PMCPMC1948013
OpenAlexW2062048603

What OpenQuestion holds

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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.