Evidence map›Paper›PMID 35665319›Full record

ArticleFrontiers in medicine2022

A Potent Histone Deacetylase Inhibitor MPT0E028 Mitigates Emphysema Severity via Components of the Hippo Signaling Pathway in an Emphysematous Mouse Model.

Lu-Yang Yeh, Yu-Ting Fang, Hong-Sheng Lee, Chia-Hao Liu, You-Yin Chen, Yu-Chun Lo, Vincent Laiman, Jing-Ping Liou, Kian Fan Chung, Hsiao-Chi Chuang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. From gut to proteomics: the impact ofFrontiers in oncology · 2025
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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

11 authors at 5 institutions in 3 countries.

Lu-Yang YehSchool of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Yu-Ting FangDepartment of Biomedical Engineering, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Hong-Sheng LeeGraduate Institute of Medical Science, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Chia-Hao LiuGraduate Institute of Medical Science, College of Medicine, Taipei Medical University, Taipei, Taiwan.
You-Yin ChenDepartment of Biomedical Engineering, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Yu-Chun LoPhD Program for Neural Regenerative Medicine, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.
Vincent LaimanInternational PhD Program in Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Jing-Ping LiouSchool of Pharmacy, College of Pharmacy, Taipei Medical University, Taipei, Taiwan.
Kian Fan ChungNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Hsiao-Chi ChuangSchool of Respiratory Therapy, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Chien-Huang LinGraduate Institute of Medical Science, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Taipei Medical University · TWNational Yang Ming Chiao Tung University · TWImperial College London · GBTaipei Medical University-Shuang Ho Hospital · TWUniversitas Gadjah Mada · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chronic obstructive pulmonary disease (COPD) is a major cause of chronic mortality. The objective of this study was to investigate the therapeutic potential of a novel potent histone deacetylase (HDAC) inhibitor MPT0E028 on emphysema. Materials and Methods: A mouse model of porcine pancreatic elastase (PPE)-induced emphysema was orally administered 0, 25, or 50 mg/kg body weight (BW) of the MPT0E028 five times/week for 3 weeks. Pulmonary function, mean linear intercept (MLI), chest CT, inflammation, yes-associated protein (YAP), transcriptional coactivator with PDZ-binding motif (TAZ), surfactant protein C (SPC), T1-α, p53, and sirtuin 1 (SIRT1) levels were examined. Results: 50 mg/kg BW of the MPT0E028 significantly decreased the tidal volume in emphysematous mice ( Conclusions: Our study showed that the potent HDAC inhibitor MPT0E028 reduced the severity and inflammation of emphysema with improvement in lung function, which could be regulated by Hippo signaling pathway. The MPT0E028 may have therapeutic potential for emphysema.

Indexed as

alveolarapoptosisCOPDHDACinflammationTAZ

Identifiers

PMID35665319
PMCPMC9157428
OpenAlexW4280559909

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.