Evidence map›Paper›PMID 26474282›Full record

ArticleOncotarget2015

Increased metastasis with loss of E2F2 in Myc-driven tumors.

Inez Yuwanita, Danielle Barnes, Michael D Monterey, Sandra O'Reilly, Eran R Andrechek

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 29 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

5 authors at 1 institution in 1 country.

Inez YuwanitaDepartment of Physiology, Michigan State University, East Lansing, MI48824, Michigan, USA.
Danielle BarnesDepartment of Physiology, Michigan State University, East Lansing, MI48824, Michigan, USA.
Michael D MontereyDepartment of Physiology, Michigan State University, East Lansing, MI48824, Michigan, USA.
Sandra O'ReillyDepartment of Physiology, Michigan State University, East Lansing, MI48824, Michigan, USA.
Eran R AndrechekDepartment of Physiology, Michigan State University, East Lansing, MI48824, Michigan, USA.
Michigan State University · US

Funding

Dissecting Tumor Heterogeneity by Analyzing Signaling Pathway Requirements.R01CA160514 · NCI · MICHIGAN STATE UNIVERSITY · PI ANDRECHEK, ERAN ROBERT · 2012 to 2016
$1.5M
NCI NIH HHS NIH R01CA160514NCI NIH HHS R01 CA160514
6 · The paper itself

Abstract

In human breast cancer, mortality is associated with metastasis to distant sites. Therefore, it is critical to elucidate the biological mechanisms that underlie tumor progression and metastasis. Using signaling pathway signatures we previously predicted a role for E2F transcription factors in Myc induced tumors. To test this role we interbred MMTV-Myc transgenic mice with E2F knockouts. Surprisingly, we observed that the loss of E2F2 sharply increased the percentage of lung metastasis in MMTV-Myc transgenic mice. Examining the gene expression profile from these tumors, we identified genetic components that were potentially involved in mediating metastasis. These genes were filtered to uncover the genes involved in metastasis that also impacted distant metastasis free survival in human breast cancer. In order to elucidate the mechanism by which E2F2 loss enhanced metastasis we generated knockdowns of E2F2 in MDA-MB-231 cells and observed increased migration in vitro and increased lung colonization in vivo. We then examined genes that were differentially regulated between tumors from MMTV-Myc, MMTV-Myc E2F2-/-, and lung metastases samples and identified PTPRD. To test the role of PTPRD in E2F2-mediated breast cancer metastasis, we generated a knockdown of PTPRD in MDA-MB-231 cells. We noted that decreased levels of PTPRD resulted in decreased migration in vitro and decreased lung colonization in vivo. Taken together, these data indicate that E2F2 loss results in increased metastasis in breast cancer, potentially functioning through a PTPRD dependent mechanism.

Indexed as

Genes, mycAnimalsBreast NeoplasmsCell MovementDisease Models, AnimalE2F2 Transcription FactorFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansLung NeoplasmsMCF-7 CellsMice, KnockoutMice, NudeMice, TransgenicE2F2 protein, humanE2f2 protein, mouseE2F2 Transcription FactorPTPRD protein, humanPtprd protein, mouseReceptor-Like Protein Tyrosine Phosphatases, Class 2E2F transcription factorsgene expressionmetastasisMMTV-MycPTPRD

Identifiers

PMID26474282
PMCPMC4741994
OpenAlexW2105309670

What OpenQuestion holds

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LicenceCC BY
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.