Evidence map›Paper›PMID 40035775›Full record

ArticleAmerican journal of respiratory cell and molecular biology2025

MOTS-c Promotes Glycolysis via AMPK-HIF-1α-PFKFB3 Pathway to Ameliorate Cardiopulmonary Bypass-induced Lung Injury.

Zihao Shen, Peng Lu, Wanjun Jin, Ziang Wen, Yuanpu Qi, Xiangyu Li, Mingyu Chu, Xin Yao, Minchao Wu, Ao Wang and 4 more

Abstract read
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In one paragraph

Article in American journal of respiratory cell and molecular biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Interplay between ischemia-reperfusion and metabolic reprogramming.Apoptosis : an international journal on programmed cell death · 2026
    Review
  3. Review
  4. Mitochondrial-derived microproteins in lung disease: insights and implications.American journal of physiology. Lung cellular and molecular physiology · 2026
    Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. A Mighty Mitochondrial Microprotein: The Protective Role of MOTS-c in Acute Lung Injury.American journal of respiratory cell and molecular biology · 2025
    Article
  10. Review
  11. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Zihao ShenDepartment of Cardiovascular Surgery and.
Peng LuDepartment of Cardiovascular Surgery and.
Wanjun JinDepartment of Cardiovascular Surgery and.
Ziang WenDepartment of Cardiovascular Surgery and.
Yuanpu QiDepartment of Cardiovascular Surgery and.
Xiangyu LiDepartment of Cardiovascular Surgery and.
Mingyu ChuDepartment of Cardiovascular Surgery and.
Xin YaoDepartment of Cardiovascular Surgery and.
Minchao WuDepartment of Cardiovascular Surgery and.
Ao WangDepartment of Cardiovascular Surgery and.
Xiao ZhangDepartment of Cardiovascular Surgery and.
Wei WangMazankowski Alberta Heart Institute, University of Alberta, Edmonton, Alberta, Canada.
Meijuan SongDepartment of Geriatrics, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Xiaowei WangDepartment of Cardiovascular Surgery and.

Funding

Key Project of Taizhou School of Clinical Medicine TZKY20220304National Natural Science Foundation of China 82470419Postgraduate Research & Practice Innovation Program of Jiangsu Province JX10214182
6 · The paper itself

Abstract

Cardiopulmonary bypass (CPB) is essential during cardiac surgery but frequently leads to lung ischemia-reperfusion injury (LIRI), a significant contributor to postoperative complications. We investigated the protective effects of mitochondrial open reading frame of the 12S ribosomal RNA type C (MOTS-c), a mitochondrial-derived peptide, against LIRI-induced acute lung injury (ALI), emphasizing glycolytic reprogramming and ferroptosis in pulmonary microvascular endothelial cells. We hypothesized that MOTS-c exerts its protective effects by regulating glycolysis and suppressing ferroptosis via metabolic signaling pathways. We conducted a prospective, controlled trial involving 107 patients undergoing CPB, evaluating plasma concentrations of MOTS-c and inflammatory markers. MOTS-c concentrations were significantly reduced in patients with ALI.

Indexed as

Acute Lung InjuryAMP-Activated Protein KinasesCardiopulmonary BypassGlycolysisHypoxia-Inducible Factor 1, alpha SubunitPhosphofructokinase-2AnimalsEndothelial CellsFemaleFerroptosisHumansMaleMiceMice, Inbred C57BLMiddle AgedOxidative StressAMP-Activated Protein KinasesHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitPFKFB3 protein, humanPhosphofructokinase-2CPBferroptosisglycolysislung ischemia–reperfusion injuryMOTS-c

Identifiers

What OpenQuestion holds

Textmetadata
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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.