Evidence map›Paper›PMID 32000296›Full record

ArticleJournal of cellular and molecular medicine2020

Verbascoside inhibits progression of glioblastoma cells by promoting Let-7g-5p and down-regulating HMGA2 via Wnt/beta-catenin signalling blockade.

Wei-Qiang Jia, Jian-Wei Zhu, Cheng-Yong Yang, Jun Ma, Tian-You Pu, Guo-Qiang Han, Ming-Ming Zou, Ru-Xiang Xu

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. TheCancers · 2025
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Bioactive Compounds ofBiomolecules · 2023
    Review
  11. Article
  12. The pharmacokinetic property and pharmacological activity of acteoside: A review.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2022
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Association ofPharmacogenomics and personalized medicine · 2021
    Article
  19. Article
  20. 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

8 authors at 3 institutions in 1 country.

Wei-Qiang JiaDepartment of Neurosurgery, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China.
Jian-Wei ZhuDepartment of Neurosurgery, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China.
Cheng-Yong YangDepartment of Neurosurgery, Guizhou Provincial People's Hospital, Guiyang, China.
Jun MaDepartment of Neurosurgery, Guizhou Provincial People's Hospital, Guiyang, China.
Tian-You PuDepartment of Neurosurgery, Guizhou Provincial People's Hospital, Guiyang, China.
Guo-Qiang HanDepartment of Neurosurgery, Guizhou Provincial People's Hospital, Guiyang, China.
Ming-Ming ZouDepartment of Neurosurgery, The Seventh Medical Center of PLA General Hospital, Beijing, China.
Ru-Xiang XuDepartment of Neurosurgery, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, China.ORCID 0000-0002-1544-5198
Guizhou Provincial People's Hospital · CNUniversity of Electronic Science and Technology of China · CNChinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) continues to show a poor prognosis despite advances in diagnostic and therapeutic approaches. The discovery of reliable prognostic indicators may significantly improve treatment outcome of GBM. In this study, we aimed to explore the function of verbascoside (VB) in GBM and its effects on GBM cell biological processes via let-7g-5p and HMGA2. Differentially expressed GBM-related microRNAs (miRNAs) were initially screened. Different concentrations of VB were applied to U87 and U251 GBM cells, and 50 µmol/L of VB was selected for subsequent experiments. Cells were transfected with let-7g-5p inhibitor or mimic, and overexpression of HMGA2 or siRNA against HMGA2 was induced, followed by treatment with VB. The regulatory relationships between VB, let-7g-5p, HMGA2 and Wnt/β-catenin signalling pathway were determined. The results showed that HMGA2 was a direct target gene of let-7g-5p. VB treatment or let-7g-5p overexpression inhibited HMGA2 expression and the activation of Wnt/β-catenin signalling pathway, which further inhibited cell viability, invasion, migration, tumour growth and promoted GBM cell apoptosis and autophagy. On the contrary, HMGA2 overexpression promoted cell viability, invasion, migration, tumour growth while inhibiting GBM cell apoptosis and autophagy. We demonstrated that VB inhibits cell viability and promotes cell autophagy in GBM cells by up-regulating let-7g-5p and down-regulating HMGA2 via Wnt/β-catenin signalling blockade.

Indexed as

Disease ProgressionAnimalsApoptosisAutophagyBase SequenceBrain NeoplasmsCell Line, TumorCell MovementCell SurvivalDown-RegulationGene Expression Regulation, NeoplasticGlioblastomaGlucosidesHMGA2 ProteinHumansMice, NudeacteosideGlucosidesHMGA2 ProteinMicroRNAsmirnlet7 microRNA, humanPhenolsPolyphenolsProtein Kinase Cautophagyglioblastomainvasionlet-7g-5pmigrationverbascosideviabilityWnt/β-catenin signalling pathway

Identifiers

PMID32000296
PMCPMC7077555
OpenAlexW3003246873

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.