Evidence map›Paper›PMID 22140473›Full record

ArticlePloS one2011

Stat3 mediates expression of autotaxin in breast cancer.

Janeen Azare, Ashley Doane, Kenneth Leslie, Qing Chang, Marjan Berishaj, Jennifer Nnoli, Kevin Mark, Hikmat Al-Ahmadie, William Gerald, Maryam Hassimi and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

49 citing papers in PubMed, 71 citations in OpenAlex.

  1. Trial
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  7. E2F7 drives autotaxin/Enpp2 transcription via chromosome looping: Repression by p53 in murine but not in human carcinomas.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
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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

14 authors at 3 institutions in 1 country.

Janeen AzareDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, United States of America.
Ashley Doane
Kenneth Leslie
Qing Chang
Marjan Berishaj
Jennifer Nnoli
Kevin Mark
Hikmat Al-Ahmadie
William Gerald
Maryam Hassimi
Agnes Viale
Mary Stracke
David Lyden
Jacqueline Bromberg
Memorial Sloan Kettering Cancer Center · USCornell University · USNational Institutes of Health · US

Funding

Role of Stat3 in Breast Cancer TumorigenesisR01CA087637 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI BROMBERG, JACQUELINE F · 2001 to 2010
$2.5M
NCI NIH HHS R01 CA087637NCI NIH HHS R01 CA87637
6 · The paper itself

Abstract

We determined that signal transducer and activator of transcription 3 (Stat3) is tyrosine phosphorylated in 37% of primary breast tumors and 63% of paired metastatic axillary lymph nodes. Examination of the distribution of tyrosine phosphorylated (pStat3) in primary tumors revealed heterogenous expression within the tumor with the highest levels found in cells on the edge of tumors with relatively lower levels in the central portion of tumors. In order to determine Stat3 target genes that may be involved in migration and metastasis, we identified those genes that were differentially expressed in primary breast cancer samples as a function of pStat3 levels. In addition to known Stat3 transcriptional targets (Twist, Snail, Tenascin-C and IL-8), we identified ENPP2 as a novel Stat3 regulated gene, which encodes autotaxin (ATX), a secreted lysophospholipase which mediates mammary tumorigenesis and cancer cell migration. A positive correlation between nuclear pStat3 and ATX was determined by immunohistochemical analysis of primary breast cancer samples and matched axillary lymph nodes and in several breast cancer derived cell lines. Inhibition of pStat3 or reducing Stat3 expression led to a decrease in ATX levels and cell migration. An association between Stat3 and the ATX promoter, which contains a number of putative Stat3 binding sites, was determined by chromatin immunoprecipitation. These observations suggest that activated Stat3 may regulate the migration of breast cancer cells through the regulation of ATX.

Indexed as

Breast NeoplasmsCell Line, TumorCluster AnalysisFemaleGene Expression Regulation, NeoplasticGenes, NeoplasmHumansLymph NodesLysophospholipase DNeoplasm MetastasisPhosphoric Diester HydrolasesPhosphorylationPhosphotyrosineSTAT3 Transcription FactorLysophospholipase DPhosphoric Diester HydrolasesPhosphotyrosineSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID22140473
PMCPMC3225372
OpenAlexW2053431943

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.