Evidence map›Paper›PMID 36716956›Full record

ReviewJournal of advanced research2023

Contribution of Nischarin/IRAS in CNS development, injury and diseases.

Peijie Zheng, Chenshu Pan, Chuntao Zhou, Bin Liu, Linlin Wang, Shiwei Duan, Yuemin Ding

Open access · goldAbstract readReview
In one paragraph

Review in Journal of advanced research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Redox Regulation of Cell Migration via Nischarin S-glutathionylation.bioRxiv : the preprint server for biology · 2025
    Article
  4. Review
  5. 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 at 2 institutions in 1 country.

Peijie ZhengDepartment of Clinical Medicine, School of Medicine, Zhejiang University City College, Hangzhou 310015, China.
Chenshu PanDepartment of Clinical Medicine, School of Medicine, Zhejiang University City College, Hangzhou 310015, China.
Chuntao ZhouDepartment of Clinical Medicine, School of Medicine, Zhejiang University City College, Hangzhou 310015, China.
Bin LiuDepartment of Clinical Medicine, School of Medicine, Zhejiang University City College, Hangzhou 310015, China.
Linlin WangDepartment of Basic Medicine Sciences, and Department of Orthopaedics of Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Shiwei DuanDepartment of Clinical Medicine, School of Medicine, Zhejiang University City College, Hangzhou 310015, China; Institute of Translational Medicine, Zhejiang University City College, Hangzhou 310015, China; Key Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, Zhejiang University City College, Hangzhou 310015, China. Electronic address: duansw@zucc.edu.cn.
Yuemin DingDepartment of Clinical Medicine, School of Medicine, Zhejiang University City College, Hangzhou 310015, China; Institute of Translational Medicine, Zhejiang University City College, Hangzhou 310015, China; Key Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, Zhejiang University City College, Hangzhou 310015, China. Electronic address: dingyuemin@zucc.edu.cn.
Zhejiang University · CNSir Run Run Shaw Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMurine Nischarin and its human homolog IRAS are scaffold proteins highly expressed in the central nervous system (CNS). Nischarin was initially discovered as a tumor suppressor protein, and recent studies have also explored its potential value in the CNS. Research on IRAS has largely focused on its effect on opioid dependence. Although the role of Nischarin/IRAS in the physiological function and pathological process of the CNS has gradually attracted attention and the related research results are expected to be applied in clinical practice, there is no systematic review of the role and mechanisms of Nischarin/IRAS in the CNS so far. AIM OF REVIEW: This review will systematically analyze the role and mechanism of Nischarin/IRAS in the CNS, and provide necessary references and possible targets for the treatment of neurological diseases, thereby broadening the direction of Nischarin/IRAS research and facilitating clinical translation. KEY SCIENTIFIC CONCEPTS OF REVIEW: The pathophysiological processes affected by dysregulation of Nischarin/IRAS expression in the CNS are mainly introduced, including spinal cord injury (SCI), opioid dependence, anxiety, depression, and autism. The molecular mechanisms such as factors regulating Nischarin/IRAS expression and signal transduction pathways regulated by Nischarin/IRAS are systematically summarized. Finally, the clinical application of Nischarin/IRAS has been prospected.

Indexed as

Intracellular Signaling Peptides and ProteinsOpioid-Related DisordersAnimalsCarrier ProteinsHumansImidazoline ReceptorsMiceSignal TransductionCarrier ProteinsImidazoline ReceptorsIntracellular Signaling Peptides and ProteinsAnxietyAutismDepressionNeurodevelopmentNischarin/IRASOpioid dependenceSpinal cord injury

Identifiers

PMID36716956
PMCPMC10703726
OpenAlexW4318305393

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.