Evidence map›Paper›PMID 36852158›Full record

ArticleDisease markers2023

Peptide ARHGEF9 Inhibits Glioma Progression via PI3K/AKT/mTOR Pathway.

Jie Huang, Xiaoling Fu, Qiang Xue, Peng Ma, Yating Yin, Minjie Jiang, Yunpeng Lu, Qi Ying, Jun Jiang, Hua He and 1 more

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Disease markers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

  • Retraction · 2023-08-09Concerns/Issues about Data · Concerns/Issues about Results and/or Conclusions · Concerns/Issues about Referencing/Attributions · Concerns/Issues about Peer Review · Informed/Patient Consent - None/Withdrawn · Investigation by Journal/Publisher · Investigation by Third Party · Lack of IRB/IACUC Approval and/or Compliance · Paper Mill · Computer-Aided Content or Computer-Generated Content · Unreliable Results and/or Conclusions · · See also: https://pubpeer.com/publications/0DD3E5B32AD589D78EC120C82A1798
  • Retracted
5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Jie HuangDepartment of Neurosurgery, Third Affiliated Hospital, Navy Medical University, Shanghai, China 200432.
Xiaoling FuDepartment of Medical Psychology, The Fourth Medical Center of PLA General Hospital, 51 Fu Cheng Road, Beijing, China 100048.
Qiang XueDepartment of Neurosurgery, Third Affiliated Hospital, Navy Medical University, Shanghai, China 200432.ORCID https://orcid.org/0000-0001-7220-4975
Peng MaDepartment of Neurosurgery, Third Affiliated Hospital, Navy Medical University, Shanghai, China 200432.
Yating YinDepartment of Neurosurgery, Third Affiliated Hospital, Navy Medical University, Shanghai, China 200432.
Minjie JiangDepartment of Neurosurgery, Yixing People's Hospital, Yixing, Jiangsu Province, China 214200.
Yunpeng LuDepartment of Neurosurgery, Yixing People's Hospital, Yixing, Jiangsu Province, China 214200.
Qi YingDepartment of Neurosurgery, Third Affiliated Hospital, Navy Medical University, Shanghai, China 200432.
Jun JiangEndoscopy Center, Minhang Hospital, Fudan University, Shanghai, China.
Hua HeDepartment of Neurosurgery, Third Affiliated Hospital, Navy Medical University, Shanghai, China 200432.ORCID https://orcid.org/0000-0001-9160-3859
Da WuDepartment of Neurosurgery, Yixing People's Hospital, Yixing, Jiangsu Province, China 214200.ORCID https://orcid.org/0000-0002-2988-9144
Jiangsu University · CNChinese PLA General Hospital · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The most prevalent malignant tumor in a human brain nervous system is called glioma. Peptide is a compound formed by the peptide bond of Method: Based on public databases, we targeted the common genes between glioma differentially expressed genes (DEGs) and peptide genes related to glioma prognosis. Then, these common genes were analyzed by LASSO-Cox analysis, prognostic risk model, and nomogram to identify key prognostic peptide genes and the target gene in this study. Next, the mechanism of target gene in glioma was explored by bioinformatics analysis and functional experiments. Results: We obtained a total of 26 overlapping genes for the following study. After that, 6 independent prognostic factors (REPIN1, PSD3, RDX, CDK4, FANCI, and ARHGEF9) were obtained and applied to construct the prognostic nomogram, and ARHGEF9 was the target gene in the study. Next, peptide ARHGEF9 was found to inhibit glioma cell development. Through Spearman's correlation analysis, ARHGEF9 had a close relation with PI3K/AKT/mTOR pathway. In functional experiments, peptide ARHGEF9 could suppress the protein expressions of p-PIK3K, p-AKT and p-mTOR, while IGF-1 could reverse this effect. Conclusion: This study identifies 6 new prognostic biomarkers for glioma patients. Among them, peptide ARHGEF9 gene is an inhibitory gene functioning by targeting PI3K/AKT/mTOR pathway.

Indexed as

Fanconi AnemiaGliomaAmino AcidsHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRho Guanine Nucleotide Exchange FactorsTOR Serine-Threonine KinasesAmino AcidsARHGEF9 protein, humanMTOR protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRho Guanine Nucleotide Exchange FactorsTOR Serine-Threonine Kinases

Identifiers

PMID36852158
PMCPMC9966571
OpenAlexW4321333010

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.