Evidence map›Paper›PMID 38984448›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Protosappanin A Protects DOX-Induced Myocardial Injury and Cardiac Dysfunction by Targeting ACSL4/FTH1 Axis-Dependent Ferroptosis.

Jingxuan Cui, Yujia Chen, Qiannan Yang, Peng Zhao, Mian Yang, Xiaoqi Wang, Ge Mang, Xiangyu Yan, Di Wang, Zhonghua Tong and 9 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing 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

79 citing papers in PubMed.

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19 more citing papers are in PubMed but not listed here.

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

19 authors.

Jingxuan CuiDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Yujia ChenDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Qiannan YangDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Peng ZhaoDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Mian YangDepartment of Cardiology Daping Hospital, The Third Military Medical, Chongqing, 400000, China.
Xiaoqi WangDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Ge MangDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Xiangyu YanDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Di WangDepartment of Cardiology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Zhonghua TongDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Penghe WangDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Yingjin KongDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Naixin WangDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Dongni WangDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Nana DongDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Mingyang LiuDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Mingyan EDepartment of Thoracic Radiotherapy, Harbin Medical University Cancer Hospital, Harbin, China.
Maomao ZhangDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.ORCID 0000-0001-5649-7931
Bo YuDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.

Funding

National Natural Science Foundation of China 82070511National Natural Science Foundation of China 82072027National Natural Science Foundation of China 82270525Natural Science Foundation of Heilongjiang Province GA23C006
6 · The paper itself

Abstract

Doxorubicin (DOX) is an effective anticancer agent, but its clinical utility is constrained by dose-dependent cardiotoxicity, partly due to cardiomyocyte ferroptosis. However, the progress of developing cardioprotective medications to counteract ferroptosis has encountered obstacles. Protosappanin A (PrA), an anti-inflammatory compound derived from hematoxylin, shows potential against DOX-induced cardiomyopathy (DIC). Here, it is reported that PrA alleviates myocardial damage and dysfunction by reducing DOX-induced ferroptosis and maintaining mitochondrial homeostasis. Subsequently, the molecular target of PrA through proteome microarray, molecular docking, and dynamics simulation is identified. Mechanistically, PrA physically binds with ferroptosis-related proteins acyl-CoA synthetase long-chain family member 4 (ACSL4) and ferritin heavy chain 1 (FTH1), ultimately inhibiting ACSL4 phosphorylation and subsequent phospholipid peroxidation, while also preventing FTH1 autophagic degradation and subsequent release of ferrous ions (Fe

Indexed as

Coenzyme A LigasesDoxorubicinFerroptosisAnimalsCardiotoxicityDisease Models, AnimalHumansMaleMiceMyocytes, CardiacAcsl4 protein, mouseCoenzyme A LigasesDoxorubicindoxorubicin‐induced cardiomyopathyferroptosismolecular targeted therapymyocardial injuryprotosappanin A

Identifiers

PMID38984448
PMCPMC11425893

What OpenQuestion holds

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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.