Evidence map›Paper›PMID 35220406›Full record

ReviewOncogene2022

The chromosome 21 kinase DYRK1A: emerging roles in cancer biology and potential as a therapeutic target.

Malini Rammohan, Ethan Harris, Rahul S Bhansali, Emily Zhao, Loretta S Li, John D Crispino

Open access · greenAbstract readReview
In one paragraph

Review in Oncogene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
9.6field-weighted citation impact, top 1% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Article
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  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. CMGC Kinases in Viral Infection and Human Disease.Pathogens (Basel, Switzerland) · 2026
    Review
  16. Article
  17. Article
  18. Article
  19. Article
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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 3 institutions in 1 country.

Malini RammohanDriskill Graduate Program in Life Sciences, Northwestern University, Chicago, IL, USA.
Ethan HarrisUniversity of Illinois at Chicago College of Medicine, Chicago, IL, USA.ORCID http://orcid.org/0000-0002-8735-1959
Rahul S BhansaliDepartment of Medicine, Division of Hematology/Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0002-3616-7393
Emily ZhaoWeinberg College of Arts and Sciences, Northwestern University, Chicago, IL, USA.
Loretta S LiMolecular and Translational Cancer Biology Program, Stanley Manne Children's Research Institute, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.
John D CrispinoDivision of Experimental Hematology, Department of Hematology, St. Jude Children's Research Hospital, Memphis, TN, USA. john.crispino@stjude.org.ORCID http://orcid.org/0000-0002-8182-8306
Northwestern University · USSt. Jude Children's Research Hospital · USHospital of the University of Pennsylvania · US

Funding

CARCINOGENESIS TRAINING PROGRAMT32CA009560 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Kathleen Janee Green · 1986 to 2026
$8.4M
Identifying the mechanisms of leukemia progressionR35CA253096 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI John D Crispino · 2021 to 2026
$6.1M
NCI NIH HHS R35 CA253096NCI NIH HHS T32 CA009560
6 · The paper itself

Abstract

Dual-specificity tyrosine phosphorylation-regulated kinase 1 A (DYRK1A) is a serine/threonine kinase that belongs to the DYRK family of proteins, a subgroup of the evolutionarily conserved CMGC protein kinase superfamily. Due to its localization on chromosome 21, the biological significance of DYRK1A was initially characterized in the pathogenesis of Down syndrome (DS) and related neurodegenerative diseases. However, increasing evidence has demonstrated a prominent role in cancer through its ability to regulate biologic processes including cell cycle progression, DNA damage repair, transcription, ubiquitination, tyrosine kinase activity, and cancer stem cell maintenance. DYRK1A has been identified as both an oncogene and tumor suppressor in different models, underscoring the importance of cellular context in its function. Here, we review mechanistic contributions of DYRK1A to cancer biology and its role as a potential therapeutic target.

Indexed as

NeoplasmsProtein Serine-Threonine KinasesProtein-Tyrosine KinasesChromosomes, Human, Pair 21Dyrk KinasesHumansOncogenesPhosphorylationDyrk KinasesProtein Serine-Threonine KinasesProtein-Tyrosine Kinases

Identifiers

PMID35220406
PMCPMC8977259
OpenAlexW4214680668

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.