Evidence map›Paper›PMID 33499468›Full record

ArticleMilitary medicine2021

MG53 as a Novel Therapeutic Protein to Treat Acute Lung Injury.

Bryan A Whitson, Kristine Mulier, Haichang Li, Xinyu Zhou, Chuanxi Cai, Sylvester M Black, Tao Tan, Jianjie Ma, Greg J Beilman

Open access · bronzeAbstract read
In one paragraph

Article in Military medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Is MG53 a potential therapeutic target for cancer?Frontiers in endocrinology · 2023
    Review
  10. MG53 attenuates nitrogen mustard-induced acute lung injury.Journal of cellular and molecular medicine · 2022
    Article
  11. Article
  12. Review
  13. Review
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

9 authors at 4 institutions in 1 country.

Bryan A WhitsonDepartment of Surgery, Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH 43210, USA.
Kristine MulierDepartment of Surgery, University of Minnesota, Minneapolis, MN 55455, USA.
Haichang LiDepartment of Surgery, Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH 43210, USA.
Xinyu ZhouDepartment of Surgery, Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH 43210, USA.
Chuanxi CaiDepartment of Surgery, Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH 43210, USA.
Sylvester M BlackDepartment of Surgery, Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH 43210, USA.
Tao TanDepartment of Surgery, Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH 43210, USA.
Jianjie MaDepartment of Surgery, Davis Heart and Lung Research Institute, The Ohio State University, Columbus, OH 43210, USA.
Greg J BeilmanDepartment of Surgery, University of Minnesota, Minneapolis, MN 55455, USA.
Lung Institute · USThe Ohio State University · USUniversity of Minnesota · USTRIM edicine (United States) · US

Funding

Preservation and Rescue of The Lung Donor Allograft for TransplantationR01HL143000 · NHLBI · OHIO STATE UNIVERSITY · PI WHITSON, BRYAN A · 2018 to 2022
$3.4M
Preservation of DCD Allograft Integrity for Liver TransplantationR01DK123475 · NIDDK · OHIO STATE UNIVERSITY · PI BLACK, SYLVESTER M · 2020 to 2024
$3.1M
NHLBI NIH HHS R01 HL143000NIDDK NIH HHS R01 DK123475
6 · The paper itself

Abstract

introductionLung injury has several inciting etiologies ranging from trauma (contusion and hemorrhage) to ischemia reperfusion injury. Reflective of the injury, tissue and cellular injury increases proportionally with the injury stress and is an area of potential intervention to mitigate the injury. This study aims to evaluate the therapeutic benefits of recombinant human MG53 (rhMG53) protein in porcine models of acute lung injury (ALI). MATERIALS AND

methodsWe utilized live cell imaging to monitor the movement of MG53 in cultured human bronchial epithelial cells following mechanical injury. The in vivo efficacy of rhMG53 was evaluated in a porcine model of hemorrhagic shock/contusive lung injury. Varying doses of rhMG53 (0, 0.2, or 1 mg/kg) were administered intravenously to pigs after induction of hemorrhagic shock/contusive induced ALI. Ex vivo lung perfusion system enabled assessment of the isolated porcine lung after a warm ischemic induced injury with rhMG53 supplementation in the perfusate (1 mg/mL).

resultsMG53-mediated cell membrane repair is preserved in human bronchial epithelial cells. rhMG53 mitigates lung injury in the porcine model of combined hemorrhagic shock/contusive lung injury. Ex vivo lung perfusion administration of rhMG53 reduces warm ischemia-induced injury to the isolated porcine lung.

conclusionsMG53 is an endogenous protein that circulates in the bloodstream. Therapeutic treatment with exogenous rhMG53 may be part of a strategy to restore (partially or completely) structural morphology and/or functional lung integrity. Systemic administration of rhMG53 constitutes a potential effective therapeutic means to combat ALI.

Indexed as

Acute Lung InjuryReperfusion InjuryAnimalsCarrier ProteinsDisease Models, AnimalLungRecombinant ProteinsSwineCarrier ProteinsRecombinant Proteins

Identifiers

PMID33499468
PMCPMC7980479
OpenAlexW3123358460

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.