Evidence map›Paper›PMID 23319807›Full record

ArticleCancer research2013

FOXP3 regulates sensitivity of cancer cells to irradiation by transcriptional repression of BRCA1.

Weiquan Li, Hiroto Katoh, Lizhong Wang, Xiaochun Yu, Zhanwen Du, Xiaoli Yan, Pan Zheng, Yang Liu

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Forkhead Box Protein P3 (FOXP3) Represses ATF3 Transcriptional Activity.International journal of molecular sciences · 2021
    Article
  3. Article
  4. FOXP3 Activates SUMO-ConjugatingInternational journal of molecular sciences · 2018
    Article
  5. Article
  6. Article
  7. BRCA1 Mutation: A Predictive Marker for Radiation Therapy?International journal of radiation oncology, biology, physics · 2015
    Review
  8. Article
  9. Foxp3 expression in T regulatory cells and other cell lineages.Cancer immunology, immunotherapy : CII · 2014
    Review
  10. Article
  11. Article
  12. IPEX Syndrome, FOXP3 and Cancer.Journal of syndromes · 2013
    Article
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

8 authors at 4 institutions in 2 countries.

Weiquan LiDepartment of Pathology, University of Michigan, Ann Arbor, MI, USA.
Hiroto Katoh
Lizhong Wang
Xiaochun Yu
Zhanwen Du
Xiaoli Yan
Pan Zheng
Yang Liu
Molecular Oncology (United States) · USChildren's National · USUniversity of Michigan–Ann Arbor · USHokkaido University · JP

Funding

Checkpoints of Host Response to Cellular InjuriesR01AI064350 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, YANG, ZHENG, PAN · 2006 to 2019
$5.6M
Tumor burden and T cell immunityR01CA058033 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, YANG · 1992 to 2013
$3.3M
FoxP3 as the X-Linked Breast Cancer Suppressor GeneR01CA120901 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, YANG · 2007 to 2010
$1.6M
NCI NIH HHS CA120901NCI NIH HHS CA58033NCI NIH HHS R01 CA058033NCI NIH HHS R01 CA120901NIAID NIH HHS R01 AI064350
6 · The paper itself

Abstract

FOXP3 is an X-linked tumor suppressor gene and a master regulator in T regulatory cell function. This gene has been found to be mutated frequently in breast and prostate cancers and to inhibit tumor cell growth, but its functional significance in DNA repair has not been studied. We found that FOXP3 silencing stimulates homologous recombination-mediated DNA repair and also repair of γ-irradiation-induced DNA damage. Expression profiling and chromatin-immunoprecipitation analyses revealed that FOXP3 regulated the BRCA1-mediated DNA repair program. Among 48 FOXP3-regulated DNA repair genes, BRCA1 and 12 others were direct targets of FOXP3 transcriptional control. Site-specific interaction of FOXP3 with the BRCA1 promoter repressed its transcription. Somatic FOXP3 mutants identified in breast cancer samples had reduced BRCA1 repressor activity, whereas FOXP3 silencing and knock-in of a prostate cancer-derived somatic FOXP3 mutant increased the radioresistance of cancer cells. Together our findings provide a missing link between FOXP3 function and DNA repair programs.

Indexed as

Gamma RaysAnimalsApoptosisBlotting, WesternBRCA1 ProteinBreast NeoplasmsCell ProliferationChromatin ImmunoprecipitationComet AssayDNA DamageDNA RepairFemaleForkhead Transcription FactorsGene Expression Regulation, NeoplasticHomologous RecombinationHumansBRCA1 ProteinForkhead Transcription FactorsFoxp3 protein, mouseRNA, Messenger

Identifiers

PMID23319807
PMCPMC3815443
OpenAlexW2091202945

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.