Evidence map›Paper›PMID 26473373›Full record

ArticleOncotarget2015

Migration-prone glioma cells show curcumin resistance associated with enhanced expression of miR-21 and invasion/anti-apoptosis-related proteins.

Wei-Lan Yeh, Hsiao-Yun Lin, Chiung-Yin Huang, Bor-Ren Huang, Chingju Lin, Dah-Yuu Lu, Kuo-Chen Wei

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

16 citing papers in PubMed, 32 citations in OpenAlex.

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  9. Differential Characterization of Temozolomide-Resistant Human Glioma Cells.International journal of molecular sciences · 2018
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  15. An integrated transcriptomic and computational analysis for biomarker identification in human glioma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
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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

7 authors at 6 institutions in 1 country.

Wei-Lan YehDepartment of Cell and Tissue Engineering, Changhua Christian Hospital, Changhua, Taiwan.
Hsiao-Yun LinGraduate Institute of Neural and Cognitive Sciences, China Medical University, Taichung, Taiwan.
Chiung-Yin HuangDepartment of Neurosurgery, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan.
Bor-Ren HuangSchool of Medicine, Tzu Chi University, Hualien, Taiwan.
Chingju LinDepartment of Physiology, School of Medicine, China Medical University, Taichung, Taiwan.
Dah-Yuu LuGraduate Institute of Neural and Cognitive Sciences, China Medical University, Taichung, Taiwan.
Kuo-Chen WeiDepartment of Neurosurgery, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan.
China Medical University · TWAsia University · TWChang Gung Memorial Hospital · TWChang Gung University · TWChanghua Christian Hospital · TWTzu Chi University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In study, the expression patterns and functional differences between an original glioma cell population (U251 and U87) and sublines (U251-P10, U87-P10) that were selected to be migration-prone were investigated. The expressions levels of VEGF and intracellular adhesion molecule-1 (ICAM-1) were increased in the migration-prone sublines as well as in samples from patients with high-grade glioma when compared to those with low-grade glioma. In addition, cells of the migration-prone sublines showed increased expression of the oncogenic microRNA. miR-21, which was also associated with more advanced clinical pathological stages in the patient tissue specimens. Treatment of U251 cells with an miR-21 mimic dramatically enhanced the migratory activity and expression of anti-apoptotic proteins. Furthermore, treatment with curcumin decreased the miR-21 level and anti-apoptotic protein expression, and increased the expression of pro-apoptosis proteins and microtubule-associated protein light chain 3-II (LC3-II) in U251 cells. The migration-prone sublines showed decreased induction of cell death markers in response to curcumin treatment. Finally, U251-P10 cells showed resistance against curcumin treatment. These results suggest that miR-21 is associated with regulation of the migratory ability and survival in human glioma cells. These findings suggest novel mechanisms of malignancy and new potential combinatorial strategies for the management of malignant glioma.

Indexed as

Antineoplastic AgentsApoptosisApoptosis Regulatory ProteinsBlotting, WesternBrain NeoplasmsCell MovementCell ProliferationCurcuminDrug Resistance, NeoplasmFlow CytometryFluorescent Antibody TechniqueGene Expression Regulation, NeoplasticGliomaHumansImmunoenzyme TechniquesMicroRNAsAntineoplastic AgentsApoptosis Regulatory ProteinsBCL2 protein, humanCurcuminMicroRNAsMIRN21 microRNA, humanProto-Oncogene Proteins c-bcl-2RNA, Messengercurcumindeath receptorgliomamigrationmiR-21

Identifiers

PMID26473373
PMCPMC4741964
OpenAlexW2267215259

What OpenQuestion holds

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LicenceCC BY
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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.