Evidence map›Paper›PMID 39707176›Full record

ReviewMolecular medicine (Cambridge, Mass.)2024

Mitochondrial uncoupling protein 2: a central player in pancreatic disease pathophysiology.

Kunpeng Wang, Lilong Zhang, Beiying Deng, Kailiang Zhao, Chen Chen, Weixing Wang

Abstract readReview
In one paragraph

Review in Molecular medicine (Cambridge, Mass.), 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. Review
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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.

Kunpeng Wang *Department of General Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Lilong Zhang *Department of General Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Beiying DengDepartment of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, China.
Kailiang ZhaoDepartment of General Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
Chen ChenDepartment of General Surgery, Renmin Hospital of Wuhan University, Wuhan, China. appreciation@whu.edu.cn.
Weixing WangDepartment of General Surgery, Renmin Hospital of Wuhan University, Wuhan, China. wangwx@whu.edu.cn.

Funding

the National Natural Science Foundation of China 82172855, and 82370654The Research support fund of Hubei Microcirculation Society HBWXH2024(1)-1
6 · The paper itself

Abstract

Pancreatic diseases pose considerable health challenges due to their complex etiology and limited therapeutic options. Mitochondrial uncoupling protein 2 (UCP2), highly expressed in pancreatic tissue, participates in numerous physiological processes and signaling pathways, indicating its potential relevance in these diseases. Despite this, UCP2's role in acute pancreatitis (AP) remains underexplored, and its functions in chronic pancreatitis (CP) and pancreatic steatosis are largely unknown. Additionally, the mechanisms connecting various pancreatic diseases are intricate and not yet fully elucidated. Given UCP2's diverse functionality, broad expression in pancreatic tissue, and the distinct pathophysiological features of pancreatic diseases, this review offers a comprehensive analysis of current findings on UCP2's involvement in these conditions. We discuss recent insights into UCP2's complex regulatory mechanisms, propose that UCP2 may serve as a central regulatory factor in pancreatic disease progression, and hypothesize that UCP2 dysfunction could significantly contribute to disease pathogenesis. Understanding UCP2's role and mechanisms in pancreatic diseases may pave the way for innovative therapeutic and diagnostic approaches.

Indexed as

Pancreatic DiseasesUncoupling Protein 2AnimalsDisease SusceptibilityGene Expression RegulationHumansMitochondriaPancreasSignal TransductionUCP2 protein, humanUncoupling Protein 2Diabetes mellitusMitochondrial uncoupling protein 2Pancreatic cancerPancreatic diseasesPancreatitisReactive oxygen species

Identifiers

PMID39707176
PMCPMC11660649

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Registered trials

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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.