Evidence map›Paper›PMID 23138933›Full record

ArticleMolecular carcinogenesis2014

Human MCS5A1 candidate breast cancer susceptibility gene FBXO10 is induced by cellular stress and correlated with lens epithelium-derived growth factor (LEDGF).

Xin Xu, David W Powell, Courtney J Lambring, Aaron H Puckett, Lucas Deschenes, Russell A Prough, Eric M Poeschla, David J Samuelson

Open access · greenAbstract read
In one paragraph

Article in Molecular carcinogenesis, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Dysregulation of arginine methylation in tumorigenesis.Frontiers in molecular biosciences · 2024
    Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Mapping Mammary Tumor Traits in the Rat.Methods in molecular biology (Clifton, N.J.) · 2019
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Roles of F-box proteins in cancer.Nature reviews. Cancer · 2014
    Review
  17. 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 2 institutions in 1 country.

Xin XuDepartment of Biochemistry and Molecular Biology, University of Louisville Health Sciences Center, Louisville, Kentucky.
David W Powell
Courtney J Lambring
Aaron H Puckett
Lucas Deschenes
Russell A Prough
Eric M Poeschla
David J Samuelson
University of Louisville · USMayo Clinic · US

Funding

LEDGF/p7 and HIV IntegrationR01AI077344 · NIAID · UNIVERSITY OF COLORADO DENVER · PI POESCHLA, ERIC M. · 2008 to 2018
$4.1M
Identifying candidate modifier elements of a breast cancer risk associated alleleR01CA137052 · NCI · UNIVERSITY OF LOUISVILLE · PI SAMUELSON, DAVID J · 2009 to 2013
$1.5M
NCI NIH HHS CA137052NCI NIH HHS R01 CA137052NIAID NIH HHS AI77344NIAID NIH HHS R01 AI077344NIDDK NIH HHS DK176743NIEHS NIH HHS P30ES01443
6 · The paper itself

Abstract

Genetic variation and candidate genes associated with breast cancer susceptibility have been identified. Identifying molecular interactions between associated genetic variation and cellular proteins may help to better understand environmental risk. Human MCS5A1 breast cancer susceptibility associated SNP rs7042509 is located in F-box protein 10 (FBXO10). An orthologous Rattus norvegicus DNA-sequence that contains SNV ss262858675 is located in rat Mcs5a1, which is part of a mammary carcinoma susceptibility locus controlling tumor development in a non-mammary cell-autonomous manner via an immune cell-mediated mechanism. Higher Fbxo10 expression in T cells is associated with Mcs5a increased susceptibility alleles. A common DNA-protein complex bound human and rat sequences containing MCS5A1/Mcs5a1 rs7042509/ss262858675 in electrophoretic mobility shift assays (EMSAs). Lens epithelium-derived growth factor (LEDGF), a stress-response protein, was identified as a candidate to bind both human and rat sequences using DNA-pulldown and mass spectrometry. LEDGF binding was confirmed by LEDGF-antibody EMSA and chromatin immunoprecipitation (ChIP). Ectopic expression of LEDGF/p75 increased luciferase activities of co-transfected reporters containing both human and rat orthologs. Over-expressed LEDGF/p75 increased endogenous FBXO10 mRNA levels in Jurkat cells, a human T-cell line, implying LEDGF may be involved in increasing FBXO10 transcript levels. Oxidative and thermal stress of Jurkat cells increased FBXO10 and LEDGF expression, further supporting a hypothesis that LEDGF binds to a regulatory region of FBXO10 and increases expression during conditions favoring carcinogenesis. We conclude that FBXO10, a candidate breast cancer susceptibility associated gene, is induced by cellular stress and LEDGF may play a role in expression of this gene.

Indexed as

Genetic Predisposition to DiseaseOxidative StressAnimalsBase SequenceBreast NeoplasmsDNA PrimersF-Box ProteinsFemaleHumansIntercellular Signaling Peptides and ProteinsJurkat CellsMolecular Sequence DataPolymerase Chain ReactionSequence Homology, Nucleic AcidDNA PrimersF-Box ProteinsIntercellular Signaling Peptides and Proteinslens epithelium-derived growth factorcomparative geneticscomplex diseasesMCS5Anon-protein-coding genetic variantsrs7042509

Identifiers

PMID23138933
PMCPMC9737042
OpenAlexW2111216934

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Read underepoch 390

Registered trials

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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.