Evidence map›Paper›PMID 40563900›Full record

ReviewBiology2025

Role of C-Jun N-Terminal Kinases on a Stressed Epithelium: Time for Testing Isoform Specificity.

Nitesh Shashikanth, Osama Alaidi, Lohitha Basa, Shreya Taank, RadhaKrishna Rao, Jayaraman Seetharaman

Abstract readReview
In one paragraph

Review in Biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Dexamethasone regulates gene expression in chondrocytes through MKP-1 and downregulates cholesterol hydroxylases CH25H and CYP7B1.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    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

6 authors.

Nitesh ShashikanthDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN 38103, USA.
Osama AlaidiDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, TN 38163, USA.ORCID 0000-0002-1292-6789
Lohitha BasaDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN 38103, USA.
Shreya TaankDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN 38103, USA.
RadhaKrishna RaoDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN 38103, USA.
Jayaraman SeetharamanDepartment of Pharmacology, Addiction Science and Toxicology, University of Tennessee Health Science Center, Memphis, TN 38103, USA.

Funding

Defining the Role of Intestinal Calcium Channels in Alcoholic Liver Damage.R01AA029270 · NIAAA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI RADHAKRISHNA RAO · 2022 to 2026
$2.5M
BLRD VA I01 BX003014NIAID NIH HHS R01AA029270NIAID NIH HHS R01AA12307
6 · The paper itself

Abstract

Biological, physiological, and psychological stressors cause a "stress response" in our bodies. Stressors that are sensorily perceived (either acute or chronic) trigger hormonal responses from the sympathetic nervous system-the SAM and HPA axis-that effect intended organs to alert the individual. Other stressors have a direct effect on the target organ(s) of the body-e.g., physical injury and wounds, toxins, ionizing, and UV radiation. Both kinds of stressors change cell equilibrium, often leading to reactive oxygen species (ROS) accumulation and cellular damage. Among the signaling pathways involved in fighting these stressors, the c-Jun-N-terminal kinases (JNK) respond to diverse kinds of stressors. This review focuses on JNK1 and JNK2, both of which are ubiquitously present in all cell types, and attention is paid to gastrointestinal tract epithelial cells and their response-including tight junction disruption and cytoskeletal changes. We discuss the seemingly opposite roles of JNK1 and JNK2 in helping cells choose pro-survival and pro-apoptotic pathways. We examine the common features of the JNK protein structure and the possibilities of discovering JNK-isoform-specific inhibitors since, although JNK1 and JNK2 are involved in multiple diseases, including cancer, obesity, diabetes, musculoskeletal and liver disease, no cell-specific or isoform-specific inhibitors are available.

Indexed as

c-Jun N-terminal Kinase (JNK)epitheliuminhibitorskinasereactive oxygen speciesstressorstructure–function relationship

Identifiers

PMID40563900
PMCPMC12189051

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.