Evidence map›Paper›PMID 27308401›Full record

ReviewMolecular & cellular oncology

DYRK1A: the double-edged kinase as a protagonist in cell growth and tumorigenesis.

P Fernández-Martínez, C Zahonero, P Sánchez-Gómez

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular & cellular oncology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
6.6field-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

66 citing papers in PubMed, 110 citations in OpenAlex.

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  7. Cell entry mechanisms of porcine enteric coronaviruses.The Journal of biological chemistry · 2026
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6 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

3 authors at 2 institutions in 1 country.

P Fernández-MartínezInstituto de Medicina Molecular Aplicada; Universidad CEU-San Pablo ; Madrid, Spain.
C ZahoneroNeuro-oncology Unit; Instituto de Salud Carlos III-UFIEC ; Madrid, Spain.
P Sánchez-GómezNeuro-oncology Unit; Instituto de Salud Carlos III-UFIEC ; Madrid, Spain.
Instituto de Salud Carlos III · ESInstituto de Medicina Molecular João Lobo Antunes

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DYRK1A (dual-specificity tyrosine-regulated kinase 1A) is a kinase with multiple implications for embryonic development, especially in the nervous system where it regulates the balance between proliferation and differentiation of neural progenitors. The DYRK1A gene is located in the Down syndrome critical region and may play a significant role in the developmental brain defects, early neurodegeneration, and cancer susceptibility of individuals with this syndrome. DYRK1A is also expressed in adults, where it might participate in the regulation of cell cycle, survival, and tumorigenesis, thus representing a potential therapeutic target for certain types of cancer. However, the final readout of DYRK1A overexpression or inhibition depends strongly on the cellular context, as it has both tumor suppressor and oncogenic activities. Here, we will discuss the functions and substrates of DYRK1A associated with the control of cell growth and tumorigenesis with a focus on the potential use of DYRK1A inhibitors in cancer therapy.

Indexed as

cancercell differentiationcell proliferationDYRK1Aneural progenitors

Identifiers

PMID27308401
PMCPMC4905233
OpenAlexW1966836247

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.