Evidence map›Paper›PMID 31221431›Full record

ReviewDifferentiation; research in biological diversity

Dickkopf1: An immunomodulatory ligand and Wnt antagonist in pathological inflammation.

Wook-Jin Chae, Alfred L M Bothwell

Open access · greenAbstract readReview
In one paragraph

Review in Differentiation; research in biological diversity. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Inflammation and DKK1-induced AKT activation contribute to endothelial dysfunction following NR2F2 loss.American journal of physiology. Lung cellular and molecular physiology · 2023
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review
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

2 authors at 1 institution in 1 country.

Wook-Jin ChaeDepartment of Immunobiology, Yale University School of Medicine, 300 Cedar Street, New Haven, CT, 06520, USA; Department of Microbiology and Immunology, Virginia Commonwealth University School of Medicine, 1101 Marshall Street, Richmond, VA, 23298, USA; Massey Cancer Center, Virginia Commonwealth University, 401 College Street, Richmond, VA, 23298, USA. Electronic address: wook-jin.chae@vcuhealth.org.
Alfred L M BothwellDepartment of Immunobiology, Yale University School of Medicine, 300 Cedar Street, New Haven, CT, 06520, USA. Electronic address: Alfred.bothwell@yale.edu.
Yale University · US

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI MEGAN C KING · 1985 to 2026
$85.0M
Regulatory T Cell Control of Intestinal TumorigenesisR01CA168670 · NCI · YALE UNIVERSITY · PI BOTHWELL, ALFRED LM · 2014 to 2018
$2.1M
Regulation of Pulmonary Inflammation in Asthma by Wnt Antagonist DKK1R21AI123858 · NIAID · YALE UNIVERSITY · PI BOTHWELL, ALFRED LM · 2017 to 2018
$461k
Regulatory T cell mediated control of colitis by Dkk1R21AI107957 · NIAID · YALE UNIVERSITY · PI BOTHWELL, ALFRED LM · 2013 to 2014
$443k
Thrombocyte Regulation of Anti-Parasite ImmunityR56AI127794 · NIAID · YALE UNIVERSITY · PI BOTHWELL, ALFRED LM · 2017 to 2017
$419k
NCI NIH HHS P30 CA016359NCI NIH HHS R01 CA168670NIAID NIH HHS R21 AI107957NIAID NIH HHS R21 AI123858NIAID NIH HHS R56 AI127794
6 · The paper itself

Abstract

The Wnt signaling pathway plays essential roles in tissue or organ homeostasis by regulating cell proliferation and differentiation. Upon tissue or organ injury, inflammation is coupled with tissue repair and regeneration process. The canonical Wnt signaling transduction pathway is crucial for cell proliferation, cell differentiation, and tissue regeneration. Dickkopf1 (DKK1) is a quintessential Wnt antagonist that inhibits the Wnt-mediated tissue repair process. Recent studies reported increased levels of DKK1 in many diseases such as cancer, infection, and musculoskeletal diseases. In many cases, the role of DKK1 has been identified as a pro-inflammatory ligand and the expression levels are associated with poor disease outcomes. A variety of cell types including platelets, endothelial cells, and cancer cells secrete DKK1 upon stimuli. This puts DKK1 in a unique place to view immune responses from multicellular interactions in tissue injury and repair process. In this review, we discuss recent efforts to address the underlying mechanism regarding the pro-inflammatory role of DKK1 in cancer, bone diseases, and other inflammatory diseases.

Indexed as

AnimalsBone DiseasesCarcinogenesisHumansImmunologic FactorsIntercellular Signaling Peptides and ProteinsWnt ProteinsWnt Signaling PathwayDKK1 protein, humanImmunologic FactorsIntercellular Signaling Peptides and ProteinsWnt Proteins

Identifiers

PMID31221431
PMCPMC6982462
OpenAlexW2949553677

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.