Evidence map›Paper›PMID 37841259›Full record

ReviewFrontiers in immunology2023

The clinical relevance of OSM in inflammatory diseases: a comprehensive review.

Cody L Wolf, Clyde Pruett, Darren Lighter, Cheryl L Jorcyk

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
15.9field-weighted citation impact, top 1% 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

62 citing papers in PubMed, 69 citations in OpenAlex.

  1. Trial
  2. Inflammatory bowel disease and breast cancer: epidemiological evidence, shared biology, and clinical management.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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2 more citing papers are in PubMed but not listed here.

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 at 1 institution in 1 country.

Cody L WolfDepartment of Biomolecular Sciences, Boise State University, Boise, ID, United States.
Clyde PruettDepartment of Biological Sciences, Boise State University, Boise, ID, United States.
Darren LighterDepartment of Biological Sciences, Boise State University, Boise, ID, United States.
Cheryl L JorcykDepartment of Biomolecular Sciences, Boise State University, Boise, ID, United States.
Boise State University · US

Funding

Women's health: interplay of maternal diet and key demographics on neurological health in the rural frontier and remote WestP20GM103408 · NIGMS · UNIVERSITY OF IDAHO · PI Scott A Minnich · 2012 to 2026
$59.8M
VPS35 D620N inhibits autophagy through disrupted hyaluronic acid-CD44 signalingP20GM109095 · NIGMS · BOISE STATE UNIVERSITY · PI OXFORD, JULIA THOM · 2014 to 2023
$22.7M
The Southwest Idaho Bridges to the BaccalaureateR25GM123927 · NIGMS · BOISE STATE UNIVERSITY · PI JORCYK, CHERYL LYNN, LYSNE, STEVEN · 2017 to 2021
$1.6M
OSM-induced IL-6 and ER status in metastatic breast cancerR15CA242471 · NCI · BOISE STATE UNIVERSITY · PI JORCYK, CHERYL LYNN · 2020 to 2020
$407k
NCI NIH HHS R15 CA242471NIGMS NIH HHS P20 GM103408NIGMS NIH HHS P20 GM109095NIGMS NIH HHS R25 GM123927
6 · The paper itself

Abstract

Oncostatin M (OSM) is a pleiotropic cytokine involved in a variety of inflammatory responses such as wound healing, liver regeneration, and bone remodeling. As a member of the interleukin-6 (IL-6) family of cytokines, OSM binds the shared receptor gp130, recruits either OSMRβ or LIFRβ, and activates a variety of signaling pathways including the JAK/STAT, MAPK, JNK, and PI3K/AKT pathways. Since its discovery in 1986, OSM has been identified as a significant contributor to a multitude of inflammatory diseases, including arthritis, inflammatory bowel disease, lung and skin disease, cardiovascular disease, and most recently, COVID-19. Additionally, OSM has also been extensively studied in the context of several cancer types including breast, cervical, ovarian, testicular, colon and gastrointestinal, brain,lung, skin, as well as other cancers. While OSM has been recognized as a significant contributor for each of these diseases, and studies have shown OSM inhibition is effective at treating or reducing symptoms, very few therapeutics have succeeded into clinical trials, and none have yet been approved by the FDA for treatment. In this review, we outline the role OSM plays in a variety of inflammatory diseases, including cancer, and outline the previous and current strategies for developing an inhibitor for OSM signaling.

Indexed as

COVID-19NeoplasmsClinical RelevanceHumansOncostatin MPhosphatidylinositol 3-KinasesOncostatin MOSM protein, humanPhosphatidylinositol 3-Kinasescancercytokinedrug developmentinflammatory diseasesmetastasisoncostatin M (OSM)oncostatin M receptor beta (OSMRβ)therapeutics

Identifiers

PMID37841259
PMCPMC10570509
OpenAlexW4387167418

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.