Evidence map›Paper›PMID 28588494›Full record

ReviewFrontiers in pharmacology2017

Myosin Light Chain Kinase: A Potential Target for Treatment of Inflammatory Diseases.

Yongjian Xiong, Chenou Wang, Liqiang Shi, Liang Wang, Zijuan Zhou, Dapeng Chen, Jingyu Wang, Huishu Guo

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
6.0field-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

45 citing papers in PubMed, 75 citations in OpenAlex.

  1. Temporal transcriptomic profiling identifies core regulators in cytokine-induced gut barrier disruption in differentiated Caco-2 cells.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Molecular Insights into the MLCK Activation by CaM.Journal of chemical information and modeling · 2023
    Article
  14. Article
  15. Transcriptome Profiling of Etridiazole-Exposed Zebrafish (International journal of molecular sciences · 2023
    Article
  16. Myosin Light-Chain Kinase Inhibition Potentiates the Antitumor Effects of Avapritinib in PDGFRA D842V-Mutant Gastrointestinal Stromal Tumor.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  17. Review
  18. Article
  19. Review
  20. Elucidating the Beneficial Effects of Ginger (ACS pharmacology & translational science · 2022
    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

8 authors at 1 institution in 1 country.

Yongjian XiongCentral Laboratory, The First Affiliated Hospital, Dalian Medical UniversityDalian, China.
Chenou WangLaboratory Animal Center, Dalian Medical UniversityDalian, China.
Liqiang ShiLaboratory Animal Center, Dalian Medical UniversityDalian, China.
Liang WangLaboratory Animal Center, Dalian Medical UniversityDalian, China.
Zijuan ZhouLaboratory Animal Center, Dalian Medical UniversityDalian, China.
Dapeng ChenLaboratory Animal Center, Dalian Medical UniversityDalian, China.
Jingyu WangLaboratory Animal Center, Dalian Medical UniversityDalian, China.
Huishu GuoCentral Laboratory, The First Affiliated Hospital, Dalian Medical UniversityDalian, China.
Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myosin light chain kinase (MLCK) induces contraction of the perijunctional apical actomyosin ring in response to phosphorylation of the myosin light chain. Abnormal expression of MLCK has been observed in respiratory diseases, pancreatitis, cardiovascular diseases, cancer, and inflammatory bowel disease. The signaling pathways involved in MLCK activation and triggering of endothelial barrier dysfunction are discussed in this review. The pharmacological effects of regulating MLCK expression by inhibitors such as ML-9, ML-7, microbial products, naturally occurring products, and microRNAs are also discussed. The influence of MLCK in inflammatory diseases starts with endothelial barrier dysfunction. The effectiveness of anti-MLCK treatment may depend on alleviation of that primary pathological mechanism. This review summarizes evidence for the potential benefits of anti-MLCK agents in the treatment of inflammatory disease and the importance of avoiding treatment-related side effects, as MLCK is widely expressed in many different tissues.

Indexed as

cancerendotheliuminflammatory bowel diseasesmyosin light chain kinasetight junctions

Identifiers

PMID28588494
PMCPMC5440522
OpenAlexW2619466966

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.