Evidence map›Paper›PMID 30962415›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2019

Phytanoyl-CoA 2-Hydroxylase-Interacting Protein-Like Gene Is a Therapeutic Target Gene for Glioblastoma Multiforme.

HuangDe Fu, Bin Ge, DuanKai Chen, YueQing Wu, QiSheng Luo, XueYu Li, ChuanHua Zheng, QianLi Tang

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

HuangDe FuDepartment of Neurosurgery, Affiliated Hospital of YouJiang Medical University for Nationalities, Baise, Guangxi, China (mainland).
Bin GeYouJiang Medical University for Nationalities, Baise, Guangxi, China (mainland).
DuanKai ChenYouJiang Medical University for Nationalities, Baise, Guangxi, China (mainland).
YueQing WuThe Fifth Affiliated Hospital of ZunYi Medical University, Zhuhai, Guangdong, China (mainland).
QiSheng LuoDepartment of Neurosurgery, Affiliated Hospital of YouJiang Medical University for Nationalities, Baise, Guangxi, China (mainland).
XueYu LiDepartment of Neurosurgery, Affiliated Hospital of YouJiang Medical University for Nationalities, Baise, Guangxi, China (mainland).
ChuanHua ZhengDepartment of Neurosurgery, Affiliated Hospital of YouJiang Medical University for Nationalities, Baise, Guangxi, China (mainland).
QianLi TangYouJiang Medical University for Nationalities, Baise, Guangxi, China (mainland).
Affiliated Hospital of Youjiang Medical University for Nationalities · CNZunyi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the most common primary CNS cancer and has a poor prognosis. This study searched for significant genes and the mechanisms involved in GBM. We used the Gene Expression Omnibus (GEO) to test the WHO normal and IV glioma database, used R tool to identify the significant gene, and finally, combined these with The Cancer Genome Atlas (TCGA) to verify the significant genes. Subsequently, we explored the biological mechanisms involved. Phytanoyl-CoA 2-hydroxylase-interacting protein-like gene (PHYHIPL) is downregulated in grade IV glioma (GBM). The downregulation of PHYHIPL in GBM is accompanied by poor overall survival in the TCGA database, which indicates that PHYHIPL is a protection gene in GBM development. Bioinformatics analysis shows that the poor prognosis with downregulated PHYHIPL may be the result of the TNF signaling pathway and the IL-17 signaling pathway, but good prognosis accompanied by upregulated PHYHIPL may be the result of retrograde endocannabinoid signaling and the cAMP signaling pathway. Protein-protein interactions (PPI) net indicated that PHYHIPL may play a vital role in cell metabolism, and we hypothesize that the downregulation mechanism may be the result of mutations of the ß-catenin gene and the endogenous siRNA, as shown in previous studies. PHYHIPL may be a target gene for the treatment and prognosis of GBM.

Indexed as

Brain NeoplasmsCoenzyme AComputational BiologyDatabases, GeneticGene Regulatory NetworksGlioblastomaGliomaHumansIntracellular Signaling Peptides and ProteinsMutationNerve Tissue ProteinsPhytanic AcidPrognosisSignal TransductionCoenzyme AIntracellular Signaling Peptides and ProteinsNerve Tissue ProteinsPHYHIPL protein, humanPhytanic Acidphytanoyl-coenzyme A

Identifiers

PMID30962415
PMCPMC6474294
OpenAlexW2937692161

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.