Evidence map›Paper›PMID 29021137›Full record

ArticleCancer research2017

DDB2 Is a Novel Regulator of Wnt Signaling in Colon Cancer.

Shuo Huang, Damiano Fantini, Bradley J Merrill, Srilata Bagchi, Grace Guzman, Pradip Raychaudhuri

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  14. Article
  15. Emerging Roles of DDB2 in Cancer.International journal of molecular sciences · 2019
    Review
  16. Wnt Signaling in vascular eye diseases.Progress in retinal and eye research · 2019
    Review
  17. Article
  18. Article
  19. Article
  20. TMEM59 potentiates Wnt signaling by promoting signalosome formation.Proceedings of the National Academy of Sciences of the United States of America · 2018
    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

6 authors at 2 institutions in 1 country.

Shuo HuangDepartment of Biochemistry and Molecular Genetics, University of Illinois, College of Medicine, Chicago, Illinois.
Damiano FantiniDepartment of Biochemistry and Molecular Genetics, University of Illinois, College of Medicine, Chicago, Illinois.
Bradley J MerrillDepartment of Biochemistry and Molecular Genetics, University of Illinois, College of Medicine, Chicago, Illinois.
Srilata BagchiDepartment of Oral Biology, College of Dentistry, University of Illinois, Chicago, Illinois. pradip@uic.edu sbagchi@uic.edu.
Grace GuzmanDepartment of Pathology, University of Illinois, Chicago, Illinois.
Pradip RaychaudhuriDepartment of Biochemistry and Molecular Genetics, University of Illinois, College of Medicine, Chicago, Illinois. pradip@uic.edu sbagchi@uic.edu.
Illinois College · USUniversity of Illinois Chicago · US

Funding

FoxM1 in liver cancer.R01CA175380 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RAYCHAUDHURI, PRADIP · 2014 to 2018
$2.0M
FoxM1 in breast cancer.R01CA177655 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RAYCHAUDHURI, PRADIP · 2014 to 2018
$1.6M
Wnt/Beta-catenin and Tcf/Lef factor regulation of pluripotencyR01HD081534 · NICHD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MERRILL, BRADLEY J · 2014 to 2018
$1.6M
DNA Damage Response and DDBR01CA156164 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BAGCHI, SRILATA, RAYCHAUDHURI, PRADIP · 2010 to 2014
$1.6M
FoxM1 in tumor cellI01BX000131 · VA · JESSE BROWN VA MEDICAL CENTER · PI RAYCHAUDHURI, PRADIP · 2009 to 2025
–
BLRD VA I01 BX000131NCI NIH HHS R01 CA156164NCI NIH HHS R01 CA175380NCI NIH HHS R01 CA177655NICHD NIH HHS R01 HD081534
6 · The paper itself

Abstract

Deregulation of the Wnt/β-catenin signaling pathway drives the development of colorectal cancer, but understanding of this pathway remains incomplete. Here, we report that the damage-specific DNA-binding protein DDB2 is critical for β-catenin-mediated activation of RNF43, which restricts Wnt signaling by removing Wnt receptors from the cell surface. Reduced expression of DDB2 and RNF43 was observed in human hyperplastic colonic foci. DDB2 recruited EZH2 and β-catenin at an upstream site in the

Indexed as

Animalsbeta CateninCell Line, TumorColonic NeoplasmsDisease Models, AnimalDNA-Binding ProteinsEnhancer of Zeste Homolog 2 ProteinEnzyme ActivationHCT116 CellsHT29 CellsHumansMaleMiceMice, KnockoutOncogene ProteinsReceptors, Wntbeta CateninDdb2 protein, mouseDNA-Binding ProteinsEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanOncogene ProteinsReceptors, WntRNA, Small InterferingRNF43 protein, humanUbiquitin-Protein Ligases

Identifiers

PMID29021137
PMCPMC5712251
OpenAlexW2764221000

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.