Evidence map›Paper›PMID 38878273›Full record

ReviewExpert opinion on therapeutic targets2024

Therapeutic perspectives on PDE4B inhibition in adipose tissue dysfunction and chronic liver injury.

Dalton W Staller, Robert G Bennett, Ram I Mahato

Abstract readReview
In one paragraph

Review in Expert opinion on therapeutic targets, 2024. 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. Article
  2. Article
  3. Review
  4. 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

3 authors.

Dalton W StallerDepartment of Cellular & Integrative Physiology, University of Nebraska Medical Center, Omaha, NE, USA.
Robert G BennettDepartment of Internal Medicine, Division of Diabetes Endocrinology and Metabolism, University of Nebraska Medical Center, Omaha, NE, USA.
Ram I MahatoDepartment of Cellular & Integrative Physiology, University of Nebraska Medical Center, Omaha, NE, USA.

Funding

Nanomedicine of Hedgehog and AKT/ERK Dual Inhibitors for Pancreatic CancerR01CA266759 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Ram I. Mahato · 2022 to 2026
$2.2M
Overcoming Resistance Mechanisms in Hedgehog and Myc-amplified MedulloblastomaR01NS116037 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI COULTER, DONALD, MAHATO, RAM I. · 2021 to 2025
$1.9M
Development and Preclinical Evaluation of Nanoformulations in Liver Fibrotic MiceR01DK135817 · NIDDK · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Ram I. Mahato, NATALIA ALEKSANDR OSNA · 2023 to 2026
$1.6M
NCI NIH HHS R01 CA266759NIDDK NIH HHS R01 DK135817NINDS NIH HHS R01 NS116037
6 · The paper itself

Abstract

introductionChronic liver disease (CLD) is a complex disease associated with profound dysfunction. Despite an incredible burden, the first and only pharmacotherapy for metabolic-associated steatohepatitis was only approved in March of this year, indicating a gap in the translation of preclinical studies. There is a body of preclinical work on the application of phosphodiesterase 4 inhibitors in CLD, none of these molecules have been successfully translated into clinical use. AREAS COVERED: To design therapies to combat CLD, it is essential to consider the dysregulation of other tissues that contribute to its development and progression. As such, proper therapies must combat this throughout the body rather than focusing only on the liver. To detail this, literature characterizing the pathogenesis of CLD was pulled from PubMed, with a particular focus placed on the role of PDE4 in inflammation and metabolism. Then, the focus is shifted to detailing the available information on existing PDE4 inhibitors. EXPERT OPINION: This review gives a brief overview of some of the pathologies of organ systems that are distinct from the liver but contribute to disease progression. The demonstrated efficacy of PDE4 inhibitors in other human inflammatory diseases should earn them further examination for the treatment of CLD.

Indexed as

Adipose TissueCyclic Nucleotide Phosphodiesterases, Type 4Phosphodiesterase 4 InhibitorsAnimalsChronic DiseaseDisease ProgressionDrug DevelopmentHumansInflammationLiver DiseasesCyclic Nucleotide Phosphodiesterases, Type 4PDE4B protein, humanPhosphodiesterase 4 InhibitorsAdiposealcoholchronic liver diseaseliver fibrosisobesityphosphodiesterase

Identifiers

PMID38878273
PMCPMC11305103

What OpenQuestion holds

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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.