Evidence map›Paper›PMID 30353649›Full record

ArticleJournal of cellular and molecular medicine2019

IL-17A promotes cell migration and invasion of glioblastoma cells via activation of PI3K/AKT signalling pathway.

Qianqian Zheng, Shuo Diao, Qi Wang, Chen Zhu, Xun Sun, Bo Yin, Xinwen Zhang, Xin Meng, Biao Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.1field-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

30 citing papers in PubMed, 49 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

9 authors at 5 institutions in 1 country.

Qianqian ZhengDepartment of Pathophysiology, College of Basic Medical Science, China Medical University, Shenyang, China.
Shuo DiaoDepartment of Neurosurgery, First Affiliated Hospital of Dalian Medical University, Dalian, China.
Qi WangDepartment of Geriatrics, The First Affiliated Hospital of China Medical University, Shenyang, China.
Chen ZhuDepartment of Neurosurgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
Xun SunDepartment of Immunology, College of Basic Medical Sciences of China Medical University, Shenyang, China.
Bo YinDepartment of Urology, ShengJing Hospital of China Medical University, Shenyang, China.
Xinwen ZhangCenter of Implant Dentistry, School & Hospital of Stomatology, China Medical University, Shenyang, China.
Xin MengDepartment of Biochemistry and Molecular Biology, College of Basic Medical Sciences of China Medical University, Shenyang, China.
Biao WangDepartment of Biochemistry and Molecular Biology, College of Basic Medical Sciences of China Medical University, Shenyang, China.ORCID 0000-0001-7691-4368
China Medical University · CNFirst Hospital of China Medical University · CNDalian Medical University · CNSheng Jing Hospital · CNStomatology Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastomas (GBMs) are the most common of both benign and malignant primary brain tumours, in which the inflammatory and immunologic abnormalities are involved. Interleukin-17A (IL-17A) plays an important role in various inflammatory diseases and cancers. Several recent studies revealed that the expression of IL-17A was overexpressed in human GBMs tissue. However, the accurate role of IL-17A in GBMs remains unclear. In this study, we aimed to explore the effect of IL-17A on cell migration and invasion of GBMs and the mechanism by which the effects occurred. We found that exogenous IL-17A promoted significantly cell migration and invasion abilities in two GBMs cell lines (U87MG and U251) in a time-dependent manner. In addition, the protein expressions of PI3K, Akt and MMP-2/9 were increased in the GBMs cells challenged by IL-17A. Furthermore, a tight junction protein ZO-1 was down-regulated but Twist and Bmi1 were up-regulated. Treatment with a PI3K inhibitor (LY294002) significantly reduced the abilities of both migration and invasion in U87MG and U251 cells. LY294002 treatment also attenuated the IL-17A causing increases of protein levels of PI3K, AKT, MMP-2/9, Twist and the decreases of protein level of ZO-1 in the U87MG and U251 cells. Taken together, we concluded that IL-17A promotes the GBM cells migration and invasion via PI3K/AKT signalling pathway. IL-17A and its related signalling pathways may be potential therapeutic targets for GBM.

Indexed as

AgedBrain NeoplasmsCell Line, TumorCell MovementFemaleGene Expression Regulation, NeoplasticGlioblastomaHumansInterleukin-17MaleMatrix Metalloproteinase 2Matrix Metalloproteinase 9Middle AgedNuclear ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktIL17A protein, humanInterleukin-17Matrix Metalloproteinase 2Matrix Metalloproteinase 9MMP2 protein, humanMMP9 protein, humanNuclear ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTWIST1 protein, humanTwist-Related Protein 1glioblastomainterleukin-17AinvasionmigrationPI3K/AKT pathway

Identifiers

PMID30353649
PMCPMC6307791
OpenAlexW2898283111

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.