Evidence map›Paper›PMID 39521734›Full record

ArticleCardiovascular toxicology2025

Isoprenaline Inhibits Histone Demethylase LSD1 to Induce Cardiac Hypertrophy.

Lili Wu, Bo Yang, Yingze Sun, Guanwei Fan, Lina Ma, Ying Ma, Xianjia Xiong, Hui Zhou, Huiping Wang, Ling Zhang and 1 more

Abstract read
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In one paragraph

Article in Cardiovascular toxicology, 2025. 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.

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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.

Lili WuDepartment Pathology and Pathophysiology, Logistics University of People's Armed Police Force, Tianjin, 300309, China.
Bo YangDepartment of Cardiology, Tianjin Beichen Hospital, Tianjin, 300134, China.
Yingze SunDepartment of Communication Engineering, College of Electronic Information and Optical Engineering, Nankai University, Tianjin, 300350, China.
Guanwei FanNational Clinical Research Center for Chinese Medicine Acupuncture and Moxibustion, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, 300193, China.
Lina MaDepartment of Health Management, Tianjin Hospital, Tianjin, 300211, China.
Ying MaSchool of Pharmacy, Tianjin Medical University, Tianjin, 300070, China.
Xianjia XiongCollege of Basic Medical Sciences, Tianjin Medical University, 22# Qixiangtai Road, Heping District, Tianjin, 300070, People's Republic of China.
Hui ZhouSchool of Pharmacy, Tianjin Medical University, Tianjin, 300070, China.
Huiping WangXuzhou Engineering Research Center of Medical Genetics and Transformation, Laboratory of Genetic Foundation and Clinical Application, Department of Genetics, Xuzhou Medical University, Xuzhou, 221004, China.
Ling ZhangCollege of Basic Medical Sciences, Tianjin Medical University, 22# Qixiangtai Road, Heping District, Tianjin, 300070, People's Republic of China. zhanglsl@tmu.edu.cn.
Bing YangCollege of Basic Medical Sciences, Tianjin Medical University, 22# Qixiangtai Road, Heping District, Tianjin, 300070, People's Republic of China. bingyang@tmu.edu.cn.

Funding

Key Research and Development Program of Xuzhou City KC22125Tianjin Beichen District Science and Technology Plan Project SHGY-2020010
6 · The paper itself

Abstract

Histone demethylation in cardiac hypertrophy is poorly understood. This study aims to determine the role of the histone demethylase LSD1 in pathological cardiac hypertrophy. Both isoprenaline (ISO)-treated and transverse aortic constriction (TAC)-treated rats developed hypertrophic hearts. LSD1 was significantly decreased; the histone marks mono- and dimethyl H3K4 and H3K9 (H3K4me1/2 and H3K9me1/2) were significantly up-regulated in the hypertrophic heart tissue, as well as the expression of the ANP, α-HMC and MLV-2v genes. An LSD1 inhibitor, OG-L002 could also induce cardiac hypertrophy and enhance the induction of cardiac hypertrophy by ISO. Overexpressed LSD1 abolished ISO-induced cardiac hypertrophy and downregulated H3K4me1/2 and H3K9me1/2 expression. Overexpression of LSD1 also reduced the expression of ANP, α-HMC and MLV-2v. In addition, we have reported isoprenaline (ISO) as one of the histone demethylase LSD1 inhibitors. This was confirmed by molecular docking, molecular dynamic studies and a histone demethylation assay. The H3K4me1/2 expression increases with the incubation of ISO in HEK 293T and HELA cells. CaMKII could be significantly activated by the LSD1 inhibitor OG-L002 as well as by ISO in rats. In summary, we have identified a novel role for LSD1 in initiating and maintaining cardiac hypertrophy.

Indexed as

CardiomegalyEnzyme InhibitorsHistone DemethylasesHypertrophy, Left VentricularIsoproterenolMyocytes, CardiacVentricular RemodelingAnimalsCalcium-Calmodulin-Dependent Protein Kinase Type 2Disease Models, AnimalHEK293 CellsHistonesHumansMaleMolecular Docking SimulationRats, Sprague-DawleyCalcium-Calmodulin-Dependent Protein Kinase Type 2Enzyme InhibitorsHistone DemethylasesHistonesIsoproterenolKDM1A protein, humanKDM1A protein, ratCardiac hypertrophyHistone demethylationIsoprenalineLSD1

Identifiers

PMID39521734

What OpenQuestion holds

Textmetadata
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.