Evidence map›Paper›PMID 39717752›Full record

ReviewFrontiers in oncology2024

Pharmacological inhibition of the MAP2K7 kinase in human disease.

H Daniel Lacorazza

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. The mechanism of the JNK signaling pathway in drug addiction : Author list.Journal of molecular medicine (Berlin, Germany) · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Expression and Clinical Significance ofInternational journal of molecular sciences · 2025
    Article
  6. Article
  7. 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

1 author.

H Daniel LacorazzaDepartment of Pathology and Immunology, Baylor College of Medicine, Houston, TX, United States.

Funding

A Molecular Approach to Dissecting MEK-Mediated Phosphorylation in Pediatric LeukemiaR01CA285402 · NCI · NORTHWESTERN UNIVERSITY · PI Daniel Lacorazza, Karl A Scheidt · 2024 to 2026
$2.0M
Targeting DYRK2 to eradicate leukemia stem cells in chronic myeloid leukemia.R01CA283079 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Daniel Lacorazza · 2024 to 2026
$1.2M
Discovery of MAP2K7 Inhibitors Through DNA-Encoded Chemical Screens to Treat T-Cell Acute Lymphoblastic LeukemiaR21CA286412 · NCI · BAYLOR COLLEGE OF MEDICINE · PI LACORAZZA, DANIEL · 2024 to 2024
$413k
NCI NIH HHS R01 CA283079NCI NIH HHS R01 CA285402NCI NIH HHS R21 CA286412
6 · The paper itself

Abstract

The MAP2K7 signaling pathway activates the c-Jun NH2-terminal protein kinase (JNK) in response to stress signals, such as inflammatory cytokines, osmotic stress, or genomic damage. While there has been interest in inhibiting JNK due to its involvement in inflammatory processes and cancer, there is increasing focus on developing MAP2K7 inhibitors to enhance specificity when MAP2K7 activation is associated with disease progression. Despite some progress, further research is needed to fully comprehend the role of MAP2K7 in cancer and assess the potential use of kinase inhibitors in cancer therapy. This review examines the role of MAP2K7 in cancer and the development of small-molecule inhibitors.

Indexed as

cancerkinase inhibitorsleukemiaMAP2K7mitogen-activated protein kinase kinase 7T-ALL

Identifiers

PMID39717752
PMCPMC11663940

What OpenQuestion holds

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LicenceCC BY
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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.