Evidence map›Paper›PMID 25379017›Full record

ArticleNeoplasia (New York, N.Y.)2014

FLI1 expression is correlated with breast cancer cellular growth, migration, and invasion and altered gene expression.

Melissa N Scheiber, Patricia M Watson, Tihana Rumboldt, Connor Stanley, Robert C Wilson, Victoria J Findlay, Paul E Anderson, Dennis K Watson

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

29 citing papers in PubMed, 70 citations in OpenAlex.

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  15. Lumefantrine, an antimalarial drug, reverses radiation and temozolomide resistance in glioblastoma.Proceedings of the National Academy of Sciences of the United States of America · 2020
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  20. Downregulation ofOncotarget · 2019
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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

8 authors at 2 institutions in 1 country.

Melissa N ScheiberDepartment of Pathology and Laboratory Medicine, The James E. Clyburn Research Center, Medical University of South Carolina, 68 President Street, Charleston, SC 29425.
Patricia M WatsonDepartment of Medicine, Division of Hematology/Oncology, The James E. Clyburn Research Center, Medical University of South Carolina, 68 President Street, Charleston, SC 29425.
Tihana RumboldtDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Children's Hospital, 171 Ashley Avenue, Charleston, SC 29425.
Connor StanleyDepartment of Computer Science, College of Charleston, Charleston, SC 29424.
Robert C WilsonDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, The James E. Clyburn Research Center, Medical University of South Carolina, 68 President Street, Charleston, SC 29425.
Victoria J FindlayDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Walton Research Building, 39 Sabin Street, Charleston, SC 29425.
Paul E AndersonDepartment of Computer Science, College of Charleston, Charleston, SC 29424.
Dennis K WatsonDepartment of Pathology and Laboratory Medicine, The James E. Clyburn Research Center, Medical University of South Carolina, 68 President Street, Charleston, SC 29425.
Medical University of South Carolina · USCollege of Charleston · US

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
THE ROLE OF FLI1 IN CELLULAR DIFFERENTIATION AND DEVELOPMENTP01CA078582 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI TROJANOWSKA, MARIA · 1998 to 2009
$9.1M
NCI NIH HHS P01 CA078582NCI NIH HHS P01CA78582NCI NIH HHS P30 CA 138313NCI NIH HHS P30 CA138313
6 · The paper itself

Abstract

ETS factors have been shown to be dysregulated in breast cancer. ETS factors control the expression of genes involved in many biological processes, such as cellular proliferation, differentiation, and apoptosis. FLI1 is an ETS protein aberrantly expressed in retrovirus-induced hematological tumors, but limited attention has been directed towards elucidating the role of FLI1 in epithelial-derived cancers. Using data mining, we show that loss of FLI1 expression is associated with shorter survival and more aggressive phenotypes of breast cancer. Gain and loss of function cellular studies indicate the inhibitory effect of FLI1 expression on cellular growth, migration, and invasion. Using Fli1 mutant mice and both a transgenic murine breast cancer model and an orthotopic injection of syngeneic tumor cells indicates that reduced Fli1 contributes to accelerated tumor growth. Global expression analysis and RNA-Seq data from an invasive human breast cancer cell line with over expression of either FLI1 and another ETS gene, PDEF, shows changes in several cellular pathways associated with cancer, such as the cytokine-cytokine receptor interaction and PI3K-Akt signaling pathways. This study demonstrates a novel role for FLI1 in epithelial cells. In addition, these results reveal that FLI1 down-regulation in breast cancer may promote tumor progression.

Indexed as

AnimalsBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMammary Neoplasms, ExperimentalMice, Inbred C57BLMice, Mutant StrainsMice, TransgenicPhosphatidylinositol 3-KinasesProto-Oncogene Protein c-fli-1Proto-Oncogene Proteins c-etsFLI1 protein, humanFli1 protein, mousePhosphatidylinositol 3-KinasesProto-Oncogene Protein c-fli-1Proto-Oncogene Proteins c-etsSPDEF protein, humanAd-FLI1, Ad-GFP-FLI1EMT, Epithelial-mesenchymal transitionER, Estrogen receptorFLI1, Friend leukemia virus integration 1GAPDH, Glyceraldehyde-3-phosphate dehydrogenaseGEO, Gene Expression OmnibusGOBO, Gene expression-based Outcome for Breast cancer OnlineIDC, Invasive ductal carcinomaIHC, ImmunohistochemistryILC, Invasive lobular carcinomaN, Normal Breast TissuePDEF, Prostate-derived ETS factorPyVT, FVB/N-Tg(MMTV-PyVT)634Mul/JRb, RetinoblastomaT, TumoruPA, Urokinase plasminogen activator

Identifiers

PMID25379017
PMCPMC4212256
OpenAlexW2128871819

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.