Evidence map›Paper›PMID 25636474›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2015

Methods to generate genetically engineered mouse models of soft tissue sarcoma.

Rebecca D Dodd, Leonor Añó, Jordan M Blum, Zhizhong Li, David Van Mater, David G Kirsch

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

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  11. Review
  12. Tumor Subtype Determines Therapeutic Response to Chimeric Polypeptide Nanoparticle-based Chemotherapy inClinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
  13. Article
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  17. NF1Cancer research · 2017
    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

6 authors.

Rebecca D DoddDuke University Medical Center, Box 91006, Durham, NC, 27708, USA.
Leonor Añó
Jordan M Blum
Zhizhong Li
David Van Mater
David G Kirsch

Funding

Center for Molecular &Cellular Studies of Ped DiseaseK12HD043494 · NICHD · DUKE UNIVERSITY · PI REED, ANN M. · 2003 to 2017
$5.2M
NICHD NIH HHS K12 HD043494
6 · The paper itself

Abstract

We discuss the generation of primary soft tissue sarcomas in mice using the Cre-loxP system to activate conditional mutations in oncogenic Kras and the tumor suppressor p53 (LSL-Kras(G12D/+); p53(flox/flox)). Sarcomas can be generated either by adenoviral delivery of Cre recombinase, activation of transgenic Cre recombinase with tamoxifen, or through transplantation of isolated satellite cells with Cre activation in vitro. Various applications of these models are discussed, including anticancer therapies, metastasis, in vivo imaging, and genetic requirements for tumorigenesis.

Indexed as

AdenoviridaeAnimalsCell SeparationCell Transformation, NeoplasticDisease Models, AnimalGenetic EngineeringIntegrasesMiceMice, TransgenicMutationProto-Oncogene Proteins p21(ras)SarcomaTamoxifenTumor Suppressor Protein p53Cre recombinaseHras protein, mouseIntegrasesProto-Oncogene Proteins p21(ras)TamoxifenTumor Suppressor Protein p53

Identifiers

PMID25636474
PMCPMC5612825

What OpenQuestion holds

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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.