Evidence map›Paper›PMID 31341204›Full record

ArticleScientific reports2019

E2F1 Drives Breast Cancer Metastasis by Regulating the Target Gene FGF13 and Altering Cell Migration.

Daniel P Hollern, Matthew R Swiatnicki, Jonathan P Rennhack, Sean A Misek, Brooke C Matson, Andrew McAuliff, Kathleen A Gallo, Kathleen M Caron, Eran R Andrechek

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

48 citing papers in PubMed, 82 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

9 authors at 2 institutions in 1 country.

Daniel P HollernLineberger Comprehensive Cancer Center University of North Carolina, Chapel Hill, United States.
Matthew R SwiatnickiDepartment of Physiology, Michigan State University, East Lansing, United States.
Jonathan P RennhackDepartment of Physiology, Michigan State University, East Lansing, United States.
Sean A MisekDepartment of Physiology, Michigan State University, East Lansing, United States.ORCID http://orcid.org/0000-0002-0246-5018
Brooke C MatsonUniversity of North Carolina Department of Cell Biology, Chapel Hill, United States.ORCID http://orcid.org/0000-0003-1979-1562
Andrew McAuliffDepartment of Physiology, Michigan State University, East Lansing, United States.
Kathleen A GalloDepartment of Physiology, Michigan State University, East Lansing, United States.
Kathleen M CaronLineberger Comprehensive Cancer Center University of North Carolina, Chapel Hill, United States.
Eran R AndrechekDepartment of Physiology, Michigan State University, East Lansing, United States. andrech1@msu.edu.
Michigan State University · USUniversity of North Carolina at Chapel Hill · US

Funding

Dissecting Tumor Heterogeneity by Analyzing Signaling Pathway Requirements.R01CA160514 · NCI · MICHIGAN STATE UNIVERSITY · PI ANDRECHEK, ERAN ROBERT · 2012 to 2016
$1.5M
Causes and Consequences of Digestive Tract LymphangiectasiaR01DK099156 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CARON, KATHLEEN M · 2013 to 2016
$1.3M
The Role of E2F2 in HER2 Positive Breast CancerK00CA212221 · NCI · DANA-FARBER CANCER INST · PI RENNHACK, JONATHAN · 2018 to 2021
$366k
The Role of E2F2 in HER2 Positive Breast CancerF99CA212221 · NCI · MICHIGAN STATE UNIVERSITY · PI RENNHACK, JONATHAN · 2016 to 2017
$85k
Illuminating the E2F Transcription Factors Control of Breast Cancer MetastasisF31CA183272 · NCI · MICHIGAN STATE UNIVERSITY · PI HOLLERN, DANIEL PATRICK · 2014 to 2014
$34k
NCI NIH HHS F31 CA183272NCI NIH HHS F99 CA212221NCI NIH HHS K00 CA212221NCI NIH HHS R01 CA160514NIDDK NIH HHS R01 DK099156U.S. Department of Health & Human Services | National Institutes of Health (NIH) F30 HD085625
6 · The paper itself

Abstract

In prior work we demonstrated that loss of E2F transcription factors inhibits metastasis. Here we address the mechanisms for this phenotype and identify the E2F regulated genes that coordinate tumor cell metastasis. Transcriptomic profiling of E2F1 knockout tumors identified a role for E2F1 as a master regulator of a suite of pro-metastatic genes, but also uncovered E2F1 target genes with an unknown role in pulmonary metastasis. High expression of one of these genes, Fgf13, is associated with early human breast cancer metastasis in a clinical dataset. Together these data led to the hypothesis that Fgf13 is critical for breast cancer metastasis, and that upregulation of Fgf13 may partially explain how E2F1 promotes breast cancer metastasis. To test this hypothesis we ablated Fgf13 via CRISPR. Deletion of Fgf13 in a MMTV-PyMT breast cancer cell line reduces colonization of the lungs in a tail vein injection. In addition, loss of Fgf13 reduced in vitro cell migration, suggesting that Fgf13 may be critical for tumor cells to escape the primary tumor and to colonize the distal sites. The significance of this work is twofold: we have both uncovered genomic features by which E2F1 regulates metastasis and we have identified new pro-metastatic functions for the E2F1 target gene Fgf13.

Indexed as

Cell MovementAnimalsCell Line, TumorE2F1 Transcription FactorFemaleFibroblast Growth FactorsGene Expression Regulation, NeoplasticMammary Neoplasms, ExperimentalMiceNeoplasm MetastasisE2f1 protein, mouseE2F1 Transcription Factorfibroblast growth factor 13Fibroblast Growth Factors

Identifiers

PMID31341204
PMCPMC6656723
OpenAlexW2963788253

What OpenQuestion holds

Textmetadata
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.