Evidence map›Paper›PMID 28144241›Full record

ReviewFrontiers in immunology2017

Phosphatase Wip1 in Immunity: An Overview and Update.

Xiao-Fei Shen, Yang Zhao, Jin-Peng Jiang, Wen-Xian Guan, Jun-Feng Du

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 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
1.6field-weighted citation impact, top 17% 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, 39 citations in OpenAlex.

  1. Article
  2. Review
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  6. Review
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  12. WIP1 phosphatase as pharmacological target in cancer therapy.Journal of molecular medicine (Berlin, Germany) · 2017
    Review
  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

5 authors at 3 institutions in 1 country.

Xiao-Fei ShenDepartment of General Surgery, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China; Transplantation Biology Research Division, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Yang ZhaoTransplantation Biology Research Division, Institute of Zoology, Chinese Academy of Sciences , Beijing , China.
Jin-Peng JiangDepartment of Rehabilitation Medicine, PLA Army General Hospital , Beijing , China.
Wen-Xian GuanDepartment of General Surgery, Affiliated Drum Tower Hospital of Nanjing University Medical School , Nanjing , China.
Jun-Feng DuDepartment of General Surgery, PLA Army General Hospital , Beijing , China.
Chinese Academy of Sciences · CNThe Military General Hospital of Beijing PLA · CNNanjing Drum Tower Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wild-type p53-induced phosphatase 1 (Wip1) is a newly identified serine/threonine phosphatase, which belongs to the PP2C family. Due to its involvement in stress-induced networks and overexpression in human tumors, primary studies have mainly focused on the role of Wip1 in tumorigenesis. It now has also been implicated in regulating several other physiological processes such as organism aging and neurogenesis. Recent evidence highlights a new role of Wip1 in controlling immune response through regulating immune cell development and function, as well as through the interplay with inflammatory signaling pathways such NF-κB and p38 mitogen-activated protein kinase. In this short review, we will give an overview of Wip1 in immunity to better understand this important phosphatase.

Indexed as

immunityinflammationsignaling pathwaystumorigenesiswild-type p53-induced phosphatase 1

Identifiers

PMID28144241
PMCPMC5239779
OpenAlexW2575777769

What OpenQuestion 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 OpenQuestion graph.