Evidence map›Paper›PMID 20460455›Full record

ArticleNucleic acids research2010

Identification of {beta}-catenin binding regions in colon cancer cells using ChIP-Seq.

Daniel Bottomly, Sydney L Kyler, Shannon K McWeeney, Gregory S Yochum

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

108 citing papers in PubMed, 156 citations in OpenAlex.

  1. Article
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  6. Signal integrator function of CXXC5 in Cancer.Cell communication and signaling : CCS · 2025
    Review
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  9. LPAAmerican journal of physiology. Gastrointestinal and liver physiology · 2024
    Article
  10. Article
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  12. TCF7L1 RegulatesGenes · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

48 more citing papers are in PubMed but not listed here.

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

4 authors at 3 institutions in 1 country.

Daniel BottomlyOregon Clinical and Translational Research Institute, Oregon Health and Science University, Portland, OR, USA.
Sydney L Kyler
Shannon K McWeeney
Gregory S Yochum
Oregon Health & Science University · USOregon Clinic · USPennsylvania State University · US

Funding

OREGON CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR024140 · NCRR · OREGON HEALTH & SCIENCE UNIVERSITY · PI ORWOLL, ERIC S. · 2006 to 2011
$61.1M
Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Luiz Eduardo Bertassoni · 1997 to 2026
$60.5M
c-Myc transcription in intestinal growth, differentiation, and carcinogenesisR01DK080805 · NIDDK · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI YOCHUM, GREGORY S. · 2008 to 2012
$1.5M
NCI NIH HHS 5 P30 CA069533-13NCRR NIH HHS 5UL1RR024140NIDDK NIH HHS R01 DK080805NIDDK NIH HHS R01DK080805
6 · The paper itself

Abstract

Deregulation of the Wnt/β-catenin signaling pathway is a hallmark of colon cancer. Mutations in the adenomatous polyposis coli (APC) gene occur in the vast majority of colorectal cancers and are an initiating event in cellular transformation. Cells harboring mutant APC contain elevated levels of the β-catenin transcription coactivator in the nucleus which leads to abnormal expression of genes controlled by β-catenin/T-cell factor 4 (TCF4) complexes. Here, we use chromatin immunoprecipitation coupled with massively parallel sequencing (ChIP-Seq) to identify β-catenin binding regions in HCT116 human colon cancer cells. We localized 2168 β-catenin enriched regions using a concordance approach for integrating the output from multiple peak alignment algorithms. Motif discovery algorithms found a core TCF4 motif (T/A-T/A-C-A-A-A-G), an extended TCF4 motif (A/T/G-C/G-T/A-T/A-C-A-A-A-G) and an AP-1 motif (T-G-A-C/T-T-C-A) to be significantly represented in β-catenin enriched regions. Furthermore, 417 regions contained both TCF4 and AP-1 motifs. Genes associated with TCF4 and AP-1 motifs bound β-catenin, TCF4 and c-Jun in vivo and were activated by Wnt signaling and serum growth factors. Our work provides evidence that Wnt/β-catenin and mitogen signaling pathways intersect directly to regulate a defined set of target genes.

Indexed as

Regulatory Elements, Transcriptionalbeta CateninBinding SitesCarrier ProteinsCell Line, TumorChromatinChromatin ImmunoprecipitationColonic NeoplasmsDNA-Binding ProteinsGenomicsHumansSequence Analysis, DNATranscription Factorsbeta CateninCarrier ProteinsChromatinCXXC5 protein, humanDNA-Binding ProteinsTranscription Factors

Identifiers

PMID20460455
PMCPMC2943592
OpenAlexW2108808690

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.