Evidence map›Paper›PMID 31010428›Full record

ArticleBMC research notes2019

Mebendazole-induced M1 polarisation of THP-1 macrophages may involve DYRK1B inhibition.

Kristin Blom, Jenny Rubin, Malin Berglund, Malin Jarvius, Lena Lenhammar, Vendela Parrow, Claes Andersson, Angelica Loskog, Mårten Fryknäs, Peter Nygren and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC research notes, 2019. 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
0.9field-weighted citation impact, top 27% 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, 18 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Mebendazole effectively overcomes imatinib resistance by dual-targeting BCR/ABL oncoprotein and β-tubulin in chronic myeloid leukemia cells.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  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

11 authors at 1 institution in 1 country.

Kristin BlomDepartment of Medical Sciences, Division of Cancer Pharmacology and Computational Medicine, Uppsala University, 75185, Uppsala, Sweden.
Jenny RubinDepartment of Medical Sciences, Division of Cancer Pharmacology and Computational Medicine, Uppsala University, 75185, Uppsala, Sweden.
Malin BerglundDepartment of Medical Sciences, Division of Cancer Pharmacology and Computational Medicine, Uppsala University, 75185, Uppsala, Sweden.
Malin JarviusDepartment of Medical Sciences, Division of Cancer Pharmacology and Computational Medicine, Uppsala University, 75185, Uppsala, Sweden.
Lena LenhammarDepartment of Medical Sciences, Division of Cancer Pharmacology and Computational Medicine, Uppsala University, 75185, Uppsala, Sweden.
Vendela ParrowDepartment of Medical Sciences, Division of Cancer Pharmacology and Computational Medicine, Uppsala University, 75185, Uppsala, Sweden.
Claes AnderssonDepartment of Medical Sciences, Division of Cancer Pharmacology and Computational Medicine, Uppsala University, 75185, Uppsala, Sweden.
Angelica LoskogDepartment of Immunology, Genetics and Pathology, Uppsala University, 75185, Uppsala, Sweden.
Mårten FryknäsDepartment of Medical Sciences, Division of Cancer Pharmacology and Computational Medicine, Uppsala University, 75185, Uppsala, Sweden.
Peter NygrenDepartment of Immunology, Genetics and Pathology, Uppsala University, 75185, Uppsala, Sweden.
Rolf LarssonDepartment of Medical Sciences, Division of Cancer Pharmacology and Computational Medicine, Uppsala University, 75185, Uppsala, Sweden. rolf.larsson@medsci.uu.se.ORCID http://orcid.org/0000-0002-3427-4128
Uppsala University · SE

Funding

Cancerfonden Can 2016/335
6 · The paper itself

Abstract

objectiveWe recently showed that the anti-helminthic compound mebendazole (MBZ) has immunomodulating activity by inducing a M2 to M1 phenotype switch in monocyte/macrophage models. In the present study we investigated the potential role of protein kinases in mediating this effect.

resultsMBZ potently binds and inhibits Dual specificity tyrosine-phosphorylation-regulated kinase 1B (DYRK1B) with a Kd and an IC

Indexed as

Antigens, CDAntigens, Differentiation, MyelomonocyticAntinematodal AgentsCD163 AntigenCell DifferentiationDyrk KinasesGene Expression RegulationHeterocyclic Compounds, 2-RingHumansInterferon-gammaInterleukinsLipopolysaccharidesMacrophagesMebendazolePhosphorylationProtein BindingABL1 protein, humanAntigens, CDAntigens, Differentiation, MyelomonocyticAntinematodal AgentsAZ191 compoundCD163 AntigenDyrk KinasesHeterocyclic Compounds, 2-RingInterferon-gammaInterleukinsLipopolysaccharidesMebendazoleProtein Kinase InhibitorsProtein Serine-Threonine KinasesProtein-Tyrosine KinasesProto-Oncogene Proteins c-ablPyrimidinesReceptors, Cell SurfaceTetradecanoylphorbol AcetateDYRK1BM1 polarisationMebendazoleMonocytes and macrophages

Identifiers

PMID31010428
PMCPMC6477744
OpenAlexW2944480511

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.