Evidence map›Paper›PMID 27484906›Full record

ArticleMolecules and cells2016

MicroRNA-203 As a Stemness Inhibitor of Glioblastoma Stem Cells.

Yifan Deng, Gang Zhu, Honghai Luo, Shiguang Zhao

Open access · diamondAbstract read
In one paragraph

Article in Molecules and cells, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Tumor heterogeneity and resistance in glioblastoma: the role of stem cells.Apoptosis : an international journal on programmed cell death · 2025
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  10. MicroRNA Signature in Human Normal and Tumoral Neural Stem Cells.International journal of molecular sciences · 2019
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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

4 authors at 1 institution in 1 country.

Yifan DengDepartment of Neurosurgery, Huizhou Municipal Central Hospital, Huizhou City, Guangdong Province, 516000, The People's Republic of China.
Gang ZhuDepartment of Neurosurgery, Huizhou Municipal Central Hospital, Huizhou City, Guangdong Province, 516000, The People's Republic of China.
Honghai LuoDepartment of Neurosurgery, Huizhou Municipal Central Hospital, Huizhou City, Guangdong Province, 516000, The People's Republic of China.
Shiguang ZhaoDepartment of Neurosurgery, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province, The People's Republic of China.
First Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma stem cells (GBM-SCs) are believed to be a subpopulation within all glioblastoma (GBM) cells that are in large part responsible for tumor growth and the high grade of therapeutic resistance that is so characteristic of GBM. MicroRNAs (miR) have been implicated in regulating the expression of oncogenes and tumor suppressor genes in cancer stem cells, including GBM-SCs, and they are a potential target for cancer therapy. In the current study, miR-203 expression was reduced in CD133(+) GBM-SCs derived from six human GBM biopsies. MicroRNA-203 transfected GBM-SCs had reduced capacity for self-renewal in the cell sphere assay and increased expression of glial and neuronal differentiation markers. In addition, a reduced proliferation rate and an increased rate of apoptosis were observed. Therefore, miR-203 has the potential to reduce features of stemness, specifically in GBM-SCs, and is a logical target for GBM gene therapy.

Indexed as

Genetic TherapyAC133 AntigenAdultApoptosisBrain NeoplasmsCarcinogenesisCell DifferentiationCell ProliferationCell Self RenewalCell SurvivalFemaleGene Expression Regulation, NeoplasticGlioblastomaHumansMaleMembrane ProteinsAC133 AntigenCKAP4 protein, humanMembrane ProteinsMicroRNAsMIRN203 microRNA, humandifferentiationglioblastoma stem cellsmiR-203self-renewal ability

Identifiers

PMID27484906
PMCPMC4990754
OpenAlexW2498284272

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.