Evidence map›Paper›PMID 41827868›Full record

ArticleCells2026

Prolonged Mitogen-Activated Protein Kinase Kinase (MEK) Inhibition Induces Increase in Proteolysis and Compensatory Phosphorylation of MEK and Protein Kinase B (AKT) in Plexiform Neurofibroma Cells.

Kyungmin Ji, John F Callaghan, Thomas J Ridella, Raymond R Mattingly

Abstract read
In one paragraph

Article in Cells, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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

4 authors.

Kyungmin JiDepartment of Neurology, Henry Ford Health System, Detroit, MI 48202, USA.ORCID 0000-0001-7336-265X
John F CallaghanDepartment of Pharmacology and Toxicology, Brody Medical School, East Carolina University, Greenville, NC 27834, USA.ORCID 0009-0009-5564-355X
Thomas J RidellaDepartment of Pharmacology, Wayne State University, Detroit, MI 48201, USA.
Raymond R MattinglyDepartment of Pharmacology, Wayne State University, Detroit, MI 48201, USA.ORCID 0000-0002-3177-3861

Funding

Neurofibromatosis Therapeutic Acceleration Program N/ANF Michigan, Inc. N/AThe Barbara Ann Karmanos Cancer Institute N/AUnited States Department of Defense NF220063United States Department of Defense W81XWH-22-1-0564
6 · The paper itself

Abstract

Plexiform neurofibromas associated with neurofibromatosis type I (pNF1s) are benign tumors caused by the complete loss of function of the

Indexed as

Mitogen-Activated Protein Kinase KinasesNeurofibroma, PlexiformProtein Kinase InhibitorsProteolysisProto-Oncogene Proteins c-aktAnimalsCell Line, TumorHumansPhosphorylationMitogen-Activated Protein Kinase KinasesProtein Kinase InhibitorsProto-Oncogene Proteins c-aktMEKmitogen-activated protein kinase kinase (MEK) inhibitionplexiform neurofibromaprotein kinase B (AKT)proteolysis

Identifiers

PMID41827868
PMCPMC12984194

What OpenQuestion holds

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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.