Evidence map›Paper›PMID 38993858›Full record

ArticleFrontiers in transplantation2023

Prolonged warm ischemia time increases mitogen-activated protein kinase activity and decreases perfusate cytokine levels in

Joohyun Kim, Seung-Keun Hong, Yongqiang Yang, Alice Lee, Karin M Hoffmeister, Benjamin N Gantner, Jong-In Park

Abstract read
In one paragraph

Article in Frontiers in transplantation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Joohyun KimDepartment of Surgery, Division of Transplant Surgery, Medical College of Wisconsin, Milwaukee, WI, United States.
Seung-Keun HongDepartment of Surgery, Division of Transplant Surgery, Medical College of Wisconsin, Milwaukee, WI, United States.
Yongqiang YangDepartment of Surgery, Division of Transplant Surgery, Medical College of Wisconsin, Milwaukee, WI, United States.
Alice LeeDepartment of Surgery, Division of Transplant Surgery, Medical College of Wisconsin, Milwaukee, WI, United States.
Karin M HoffmeisterVersiti Translational Glycomics Center, Blood Research Institute and Medical College of Wisconsin, Milwaukee, WI, United States.
Benjamin N GantnerDepartment of Medicine, Division of Endocrinology, Medical College of Wisconsin, Milwaukee, WI, United States.
Jong-In ParkDepartment of Biochemistry, Medical College of Wisconsin, Milwaukee, WI, United States.

Funding

Clinical and Translational Science AwardUL1TR001436 · NCATS · MEDICAL COLLEGE OF WISCONSIN · PI FREED, JULIE K · 2015 to 2025
$47.5M
NCATS NIH HHS UL1 TR001436
6 · The paper itself

Abstract

Introduction: Machine perfusion is increasingly being utilized in liver transplantation in lieu of traditional cold static organ preservation. Nevertheless, better understanding of the molecular mechanisms underlying the ischemia-reperfusion injury (IRI) during Methods: Male Sprague-Dawley rats underwent Results: Our data revealed a strong correlation between incremental WIT and a series of liver injury markers, and that prolonged WIT increases ERK1/2 and p54 JNK phosphorylation during machine perfusion. Notably, specific cytokine levels (MCP-1, MIP-2, GRO/KC, IL-10, and IL-5) were inversely correlated with the phosphorylation levels of ERK1/2, p38 MAPK, and p46/p54 JNK. Discussion: These results suggest that MAPK activation, specifically ERK1/2 and p54 JNK phosphorylation, have potential as a biomarker for hepatic IRI pathophysiology during machine perfusion. Elucidation of their functional significance may lead to designing a novel strategy to increase the clinical benefit of machine perfusion.

Indexed as

chemokinecytokineliver viabilitymachine perfusionwarm ischemia time

Identifiers

PMID38993858
PMCPMC11235240

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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.