Evidence map›Paper›PMID 20678582›Full record

ReviewThe international journal of biochemistry & cell biology2010

Signalling through FOXP3 as an X-linked tumor suppressor.

Hiroto Katoh, Pan Zheng, Yang Liu

Open access · greenAbstract readReview
In one paragraph

Review in The international journal of biochemistry & cell biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

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  18. FOXP3 as an X-linked tumor suppressor.Discovery medicine · 2010
    Review
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.

Hiroto KatohDivision of Immunotherapy, Department of Surgery, University of Michigan School of Medicine and Cancer Center, Ann Arbor, MI 48109, USA.
Pan Zheng
Yang Liu
University of Michigan–Ann Arbor · US

Funding

FoxP3 as the X-Linked Breast Cancer Suppressor GeneR01CA120901 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, YANG · 2007 to 2010
$1.6M
CD24 Polymorphism and Acetaminophen ToxicityRC1GM091648 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHENG, PAN · 2009 to 2010
$998k
NCI NIH HHS R01 CA120901NIGMS NIH HHS RC1 GM091648
6 · The paper itself

Abstract

The FOXP3 (forkhead box P3) gene is a member of forkhead winged helix family transcription factors and functions as both a transcriptional activator and a repressor. FOXP3 dysfunction is responsible for an X-linked autoimmune syndrome: immune dysregulation, polyendopathy, enterophathy, X-linked syndrome. In addition to its role as an essential transcription factor in regulatory T cells, the FOXP3 gene is an epithelial cell-intrinsic tumor suppressor for breast and prostate cancers. We will focus on the FOXP3 signalling pathway in epithelial cells and discuss how genetic and/or epigenetic inactivation of the FOXP3 contributes to the malignant transformation of cells.

Indexed as

AnimalsBreast NeoplasmsFemaleForkhead Transcription FactorsGenes, Tumor SuppressorGenes, X-LinkedHumansMaleProstatic NeoplasmsForkhead Transcription Factors

Identifiers

PMID20678582
PMCPMC2950213
OpenAlexW2086782898

What OpenQuestion holds

Textmetadata
LicenceTDM
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.