Evidence map›Paper›PMID 20551321›Full record

ArticleThe Journal of biological chemistry2010

Genome-wide analysis of CDX2 binding in intestinal epithelial cells (Caco-2).

Mette Boyd, Morten Hansen, Tine G K Jensen, Anna Perearnau, Anders K Olsen, Lotte L Bram, Mads Bak, Niels Tommerup, Jørgen Olsen, Jesper T Troelsen

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Intestinal Wnt in the transition from physiology to oncology.World journal of clinical oncology · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. International journal of molecular sciences · 2020
    Article
  12. Article
  13. HNF4α and CDX2 Regulate IntestinalInternational journal of molecular sciences · 2019
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

10 authors at 1 institution in 1 country.

Mette BoydDepartment of Cellular and Molecular Medicine, Panum Institute, Building 6.4, University of Copenhagen, Blegdamsvej 3. 2200 Copenhagen N, Denmark.
Morten Hansen
Tine G K Jensen
Anna Perearnau
Anders K Olsen
Lotte L Bram
Mads Bak
Niels Tommerup
Jørgen Olsen
Jesper T Troelsen
University of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CDX2 transcription factor is known to play a crucial role in inhibiting proliferation, promoting differentiation and the expression of intestinal specific genes in intestinal cells. The overall effect of CDX2 in intestinal cells has previously been investigated in conditional knock-out mice, revealing a critical role of CDX2 in the formation of the normal intestinal identity. The identification of direct targets of transcription factors is a key problem in the study of gene regulatory networks. The ChIP-seq technique combines chromatin immunoprecipitation (ChIP) with next generation sequencing resulting in a high throughput experimental method of identifying direct targets of specific transcription factors. The method was applied to CDX2, leading to the identification of the direct binding of CDX2 to several known and novel target genes in the intestinal cell. Examination of the transcript levels of selected genes verified the regulatory role of CDX2 binding. The results place CDX2 as a key node in a transcription factor network controlling the proliferation and differentiation of intestinal cells.

Indexed as

Caco-2 CellsCDX2 Transcription FactorCell DifferentiationChromatin ImmunoprecipitationComputational BiologyElectrophoretic Mobility Shift AssayEnhancer Elements, GeneticEpithelial CellsGenome, HumanHepatocyte Nuclear Factor 4High Mobility Group ProteinsHomeodomain ProteinsHumansIntestinesMembrane ProteinsMetalloendopeptidasesCDX2 Transcription FactorHBP1 protein, humanHepatocyte Nuclear Factor 4HEPH protein, humanHigh Mobility Group ProteinsHomeodomain ProteinsMembrane Proteinsmeprin AMetalloendopeptidasesRepressor ProteinsTrans-Activators

Identifiers

PMID20551321
PMCPMC2919073
OpenAlexW1979165357

What OpenQuestion holds

Textmetadata
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.