Evidence map›Paper›PMID 31015365›Full record

ArticleBioscience reports2019

Pristimerin inhibits glioma progression by targeting AGO2 and PTPN1 expression via miR-542-5p.

Zaiyu Li, Cong Hu, Yu Zhen, Bo Pang, Huanfa Yi, Xianglin Chen

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. MicroRNA Dysregulation in Prostate Cancer.Pharmacogenomics and personalized medicine · 2022
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Terpenoids, Cannabimimetic Ligands, beyond theMolecules (Basel, Switzerland) · 2020
    Review
  15. Article
  16. Article
  17. Review
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

6 authors at 2 institutions in 1 country.

Zaiyu LiDepartment of Neurosurgery, The Sixth Hospital Affiliated to Guangzhou Medical University, Qingyuan, Guangdong, 511500, China.
Cong HuCentral Laboratory of the Eastern Division, The First Hospital of Jilin University, Changchun, Jilin 130021, China.ORCID 0000-0002-8595-4713
Yu ZhenDepartment of Dermatology, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
Bo PangDepartment of Cardiology, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
Huanfa YiCentral Laboratory of the Eastern Division, The First Hospital of Jilin University, Changchun, Jilin 130021, China.
Xianglin ChenDepartment of Neurosurgery, The Sixth Hospital Affiliated to Guangzhou Medical University, Qingyuan, Guangdong, 511500, China xianglinchen007@163.com.ORCID 0000-0001-5088-7103
Jilin University · CNGuangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiform is the most common and malignant primary tumor of the central nervous system in adults, the high recurrence rate and poor prognosis are critical priorities. Pristimerin is a naturally occurring quinone methide triterpenoid isolated from the Celastraceae and Hippocrateaceae families. Its anticancer effects have garnered considerable attention; nonetheless, the mechanisms of action remain unknown. To predict the hub genes of pristimerin, PharmMapper and the Coremine database were used to identify 13 potential protein targets; protein-protein interaction, for which functional enrichment analyses were performed. Compound-target, target-pathway, and compound-target-pathway networks were constructed using Cytoscape. Biological process analysis first revealed that enrichment of these target genes correlated with negative regulation of symbiont growth in the host, and regulation of chronic inflammatory response to antigenic stimulus. Survival analysis in cBioPortal showed that protein tyrosine phosphatase, non-receptor type 1 (PTPN1) and Argonaute 2 (AGO2) might be involved in the carcinogenesis, invasion, or recurrence of diffuse glioma. In addition, we observed that low-dose pristimerin inhibited the viability of glioma cells, while miR-542-5p

Indexed as

AnimalsAntineoplastic AgentsArgonaute ProteinsCell Line, TumorDisease ProgressionGene Expression Regulation, NeoplasticGlioblastomaHumansMiceMicroRNAsPentacyclic TriterpenesProtein Tyrosine Phosphatase, Non-Receptor Type 1TriterpenesAGO2 protein, humanAntineoplastic AgentsArgonaute ProteinscelastrolMicroRNAsMIRN542 microRNA, humanPentacyclic TriterpenesProtein Tyrosine Phosphatase, Non-Receptor Type 1PTPN1 protein, humanTriterpenesAGO2anti-cancerglioma cellsmiRNAPritimerinPTPN1

Identifiers

PMID31015365
PMCPMC6522714
OpenAlexW2941395708

What OpenQuestion holds

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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.