Evidence map›Paper›PMID 12082548›Full record

ArticleNeoplasia (New York, N.Y.)

STAT6 mediates interleukin-4 growth inhibition in human breast cancer cells.

Jennifer L Gooch, Barbara Christy, Douglas Yee

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

43 citing papers in PubMed, 84 citations in OpenAlex.

  1. Article
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  5. Cell Death: Mechanisms and Potential Targets in Breast Cancer Therapy.International journal of molecular sciences · 2024
    Review
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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

3 authors at 1 institution in 1 country.

Jennifer L GoochDepartment of Medicine, Division of Oncology, University of Texas Health Science Center, San Antonio, TX 78284, USA.
Barbara Christy
Douglas Yee
The University of Texas Health Science Center at San Antonio · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Lei Zheng · 1991 to 2026
$59.1M
TARGETING THE IGF SYSTEM IN BREAST CANCERR01CA074285 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI YEE, DOUGLAS · 1998 to 2012
$4.0M
NCI NIH HHS P30 CA054174NCI NIH HHS P30 CA 54174NCI NIH HHS R01 CA074285NCI NIH HHS R01 CA 74285
6 · The paper itself

Abstract

In addition to acting as a hematopoietic growth factor, interleukin-4 (IL-4) inhibits growth of some transformed cells in vitro and in vivo. In this study, we show that insulin receptor substrate (IRS)-1, IRS-2, and signal transducer and activator of transcription 6 (STAT6) are phosphorylated following IL-4 treatment in MCF-7 breast cancer cells. STAT6 DNA binding is enhanced by IL-4 treatment. STAT6 activation occurs even after IRS-1 depletion, suggesting the two pathways are independent. To examine the role of STAT6 in IL-4-mediated growth inhibition and apoptosis, a full-length STAT6 cDNA was transfected into MCF-7 cells. Transient overexpression of STAT6 resulted in both cytoplasmic and nuclear expression of the protein, increased DNA binding in response to IL-4, and increased transactivation of an IL-4 responsive promoter. In STAT6-transfected cells, basal proliferation was reduced whereas apoptosis was increased. Finally, stable expression of STAT6 resulted in reduced foci formation compared to vector-transfected cells alone. These results suggest STAT6 is required for IL-4-mediated growth inhibition and induction of apoptosis in human breast cancer cells.

Indexed as

AdenocarcinomaApoptosisBreast NeoplasmsCell DivisionDNA, ComplementaryFemaleGrowth InhibitorsHumansInsulin Receptor Substrate ProteinsInterleukin-4Intracellular Signaling Peptides and ProteinsNeoplasm ProteinsPhosphoproteinsPhosphorylationProtein Processing, Post-TranslationalRecombinant Fusion ProteinsDNA, ComplementaryGrowth InhibitorsInsulin Receptor Substrate ProteinsInterleukin-4Intracellular Signaling Peptides and ProteinsIRS1 protein, humanIRS2 protein, humanNeoplasm ProteinsPhosphoproteinsRecombinant Fusion ProteinsSTAT6 protein, humanSTAT6 Transcription FactorTrans-Activators

Identifiers

PMID12082548
PMCPMC1531710
OpenAlexW2060976085

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.