Evidence map›Paper›PMID 20930144›Full record

ArticleJournal of cell science2010

ATF3, an adaptive-response gene, enhances TGF{beta} signaling and cancer-initiating cell features in breast cancer cells.

Xin Yin, Christopher C Wolford, Yi-Seok Chang, Stephen J McConoughey, Stephen A Ramsey, Alan Aderem, Tsonwin Hai

Abstract read
In one paragraph

Article in Journal of cell science, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

85 citing papers in PubMed, 162 citations in OpenAlex.

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  19. Tracking of Melanoma Cell Plasticity by Transcriptional Reporters.International journal of molecular sciences · 2022
    Article
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25 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Xin YinThe Ohio State Biochemistry Program, The Ohio State University, Columbus, OH 43210, USA.
Christopher C Wolford
Yi-Seok Chang
Stephen J McConoughey
Stephen A Ramsey
Alan Aderem
Tsonwin Hai
The Ohio State University · USInstitute for Systems Biology · US

Funding

Ohio State Neuroscience Centr CoreP30NS045758 · NINDS · OHIO STATE UNIVERSITY · PI OBRIETAN, KARL H · 2004 to 2015
$7.7M
LPS REGULATION OF MACROPHAGE FUNCTIONR01AI025032 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI ADEREM, ALAN A · 1987 to 2016
$6.7M
ATF3 and iNOS in Islet Distruction and Graft RejectionR01DK064938 · NIDDK · OHIO STATE UNIVERSITY · PI HAI, TSONWIN · 2006 to 2010
$1.1M
ATF3, a stress-inducible gene, in tumorigenesis and metastasisR01CA118306 · NCI · OHIO STATE UNIVERSITY · PI HAI, TSONWIN · 2008 to 2011
$1.0M
NCI NIH HHS R01 CA118306NIAID NIH HHS R01 AI025032NIDDK NIH HHS DK064938S1NIDDK NIH HHS R01 DK064938NINDS NIH HHS P30 NS045758NINDS NIH HHS P30-NS045758
6 · The paper itself

Abstract

The activating transcription factor 3 (ATF3) gene is induced by a variety of signals, including many of those encountered by cancer cells. We present evidence that ATF3 is induced by TGFβ in the MCF10CA1a breast cancer cells and plays an integral role for TGFβ to upregulate its target genes snail, slug and twist, and to enhance cell motility. Furthermore, ATF3 upregulates the expression of the TGFb gene itself, forming a positive-feedback loop for TGFβ signaling. Functionally, ectopic expression of ATF3 leads to morphological changes and alterations of markers consistent with epithelial-to-mesenchymal transition (EMT). It also leads to features associated with breast-cancer-initiating cells: increased CD24(low)-CD44(high) population of cells, mammosphere formation and tumorigenesis. Conversely, knockdown of ATF3 reduces EMT, CD24(low)-CD44(high) cells and mammosphere formation. Importantly, knocking down twist, a downstream target, reduces the ability of ATF3 to enhance mammosphere formation, indicating the functional significance of twist in ATF3 action. To our knowledge, this is the first report demonstrating the ability of ATF3 to enhance breast cancer-initiating cell features and to feedback on TGFβ. Because ATF3 is an adaptive-response gene and is induced by various stromal signals, these findings have significant implications for how the tumor microenvironment might affect cancer development.

Indexed as

Signal TransductionActivating Transcription Factor 3Breast NeoplasmsCD24 AntigenCell Line, TumorChromatin ImmunoprecipitationEpithelial-Mesenchymal TransitionFemaleFlow CytometryGene Expression Regulation, NeoplasticHumansHyaluronan ReceptorsImmunoblottingImmunoprecipitationNeoplastic Stem CellsReverse Transcriptase Polymerase Chain ReactionActivating Transcription Factor 3CD24 AntigenHyaluronan ReceptorsTransforming Growth Factor beta

Identifiers

PMID20930144
PMCPMC2951469
OpenAlexW1983661286

What OpenQuestion holds

Textmetadata
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.