Evidence map›Paper›PMID 38114486›Full record

ArticleCell death discovery2023

Upregulation of Hsp27 via further inhibition of histone H2A ubiquitination confers protection against myocardial ischemia/reperfusion injury by promoting glycolysis and enhancing mitochondrial function.

Pilong Shi, Jiawei Wu, Minghui Li, Yonggang Cao, Jiabi Wu, Ping Ren, Kai Liu, Jiajun Zhou, Yuetong Sha, Qianhui Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 23 citations in OpenAlex.

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  17. Epigenetics in Heart Failure.International journal of molecular sciences · 2024
    Review
  18. Pharmacological targeting of adaptor proteins in chronic inflammation.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Review
  19. Article
  20. 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

11 authors at 1 institution in 1 country.

Pilong Shi *Department of Pharmacology, Harbin Medical University-Daqing, Daqing, Heilongjiang, 163319, China.
Jiawei Wu *Department of Pharmacology, Harbin Medical University-Daqing, Daqing, Heilongjiang, 163319, China.
Minghui Li *Department of Pharmaceutics, Harbin Medical University-Daqing, Daqing, Heilongjiang, 163319, China.
Yonggang CaoDepartment of Pharmacology, Harbin Medical University-Daqing, Daqing, Heilongjiang, 163319, China.
Jiabi WuDepartment of Pharmacology, Harbin Medical University-Daqing, Daqing, Heilongjiang, 163319, China.
Ping RenDepartment of Pharmacology, Harbin Medical University-Daqing, Daqing, Heilongjiang, 163319, China.
Kai LiuDepartment of Pharmacology, Harbin Medical University-Daqing, Daqing, Heilongjiang, 163319, China.
Jiajun ZhouDepartment of Pharmacology, Harbin Medical University-Daqing, Daqing, Heilongjiang, 163319, China.
Yuetong ShaDepartment of Pharmacology, Harbin Medical University-Daqing, Daqing, Heilongjiang, 163319, China.
Qianhui ZhangDepartment of Pharmacology, Harbin Medical University-Daqing, Daqing, Heilongjiang, 163319, China.
Hongli SunDepartment of Pharmacology, Harbin Medical University-Daqing, Daqing, Heilongjiang, 163319, China. sunhongli@hmudq.edu.cn.ORCID http://orcid.org/0000-0001-8844-2353
Harbin Medical University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82173810
6 · The paper itself

Abstract

Research suggests that ischemic glycolysis improves myocardial tolerance to anoxia and low-flow ischemia. The rate of glycolysis during ischemia reflects the severity of the injury caused by ischemia and subsequent functional recovery following reperfusion. Histone H2AK119 ubiquitination (H2Aub) is a common modification that is primarily associated with gene silencing. Recent studies have demonstrated that H2Aub contributes to the development of cardiovascular diseases. However, the underlying mechanism remains unclear. This study identified Hsp27 (heat shock protein 27) as a H2Aub binding protein and explored its involvement in mediating glycolysis and mitochondrial function. Functional studies revealed that inhibition of PRC1 (polycomb repressive complex 1) decreased H2Aub occupancy and promoted Hsp27 expression through inhibiting ubiquitination. Additionally, it increased glycolysis by activating the NF-κB/PFKFB3 signaling pathway during myocardial ischemia. Furthermore, Hsp27 reduced mitochondrial ROS production by chaperoning COQ9, and suppressed ferroptosis during reperfusion. A delivery system was developed based on PCL-PEG-MAL (PPM)-PCM-SH (CWLSEAGPVVTVRALRGTGSW) to deliver PRT4165 (PRT), a potent inhibitor of PRC1, to damaged myocardium, resulting in decreased H2Aub. These findings revealed a novel epigenetic mechanism connecting glycolysis and ferroptosis in protecting the myocardium against ischemia/reperfusion injury.

Identifiers

PMID38114486
PMCPMC10730859
OpenAlexW4389934344

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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.