Evidence map›Paper›PMID 28726782›Full record

ArticleCell death & disease2017

PKCζ phosphorylates TRAF2 to protect against intestinal ischemia-reperfusion-induced injury.

Wei Zhou, Jihong Yao, Guangzhi Wang, Zhao Chen, Zhenlu Li, Dongcheng Feng, Yang Li, Wasim Qasim, Wenzhi Tan, Shili Ning and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. 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
0.9field-weighted citation impact, top 26% 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, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Roles of TRAFs in Ischemia-Reperfusion Injury.Frontiers in cell and developmental biology · 2020
    Review
  11. Article
  12. Article
  13. 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

11 authors at 1 institution in 1 country.

Wei ZhouDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116023, China.
Jihong YaoDepartment of Pharmacology, Dalian Medical University, Dalian 116044, China.
Guangzhi WangDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116023, China.
Zhao ChenDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116023, China.
Zhenlu LiDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116023, China.
Dongcheng FengDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116023, China.
Yang LiDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116023, China.
Wasim QasimDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116023, China.
Wenzhi TanDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116023, China.
Shili NingDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116023, China.
Xiaofeng TianDepartment of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116023, China.ORCID 0000-0002-6654-2270
Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intestinal ischemia-reperfusion (I/R) is a common clinical problem that occurs during various clinical pathological processes. Excessive apoptosis has an indispensable role in intestinal I/R injury. Tumor necrosis factor receptor-associated factor 2 (TRAF2) and PKCζ have an essential role in apoptosis. Here, we aimed to investigate the effects of PKCζ and TRAF2 and to explore the correlation between PKCζ and TRAF2 in intestinal I/R injury. Mice were subjected to intestinal I/R injury in vivo. In vitro experiments were conducted by treating Caco-2 cells with hypoxia/reoxygenation (H/R) stimulation to simulate intestinal I/R. Intestinal tissue samples and Caco-2 cells were examined using various approaches. Intestinal I/R induced the membrane translocation and phosphorylation of PKCζ. Pretreatment with the PKCζ activator phosphatidylcholine remarkably attenuated gut injury by suppressing apoptosis. H/R induced PKCζ to combine with TRAF2, which was phosphorylated by PKCζ at Ser

Indexed as

AnimalsCaco-2 CellsHumansIntestinal DiseasesMaleMicePhosphorylationProtein Kinase CProtein Kinase C zetaReperfusion InjuryTNF Receptor-Associated Factor 2Protein Kinase CProtein Kinase C zetaPSMD2 protein, humanTNF Receptor-Associated Factor 2TRAF2 protein, mouse

Identifiers

PMID28726782
PMCPMC5550857
OpenAlexW2941590777

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.