Evidence map›Paper›PMID 31953610›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2020

RNF213 suppresses carcinogenesis in glioblastoma by affecting MAPK/JNK signaling pathway.

X Wang, M Ye, M Wu, H Fang, B Xiao, L Xie, X Zhu

Abstract read
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Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2020. 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
1.3field-weighted citation impact, top 20% 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, 24 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

7 authors at 1 institution in 1 country.

X WangDepartment of Neurosurgery, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
M YeDepartment of Neurosurgery, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
M WuDepartment of Neurosurgery, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
H FangDepartment of Neurosurgery, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
B XiaoDepartment of Neurosurgery, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
L XieDepartment of Neurosurgery, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
X ZhuDepartment of Neurosurgery, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China. xgzhu_07@aliyun.com.ORCID http://orcid.org/0000-0002-8993-009X
Nanchang University · CN

Funding

Construction Plan of the Superior Science and Technology Innovation Team of Jiangxi Province No.20152BCB24009Foreign Science and Technology Cooperation Plan of Jiangxi Province No.20151BDH8009Key Project of Jiangxi Natural Science Foundation No.20171ACB20035National Natural Science Foundation of China No.81660420National Natural Science Foundation of China No.81760446
6 · The paper itself

Abstract

purposeGlioblastoma is the most common malignant brain tumor in central nervous system. Due to absence of the mechanism underlying glioblastoma, the clinical outcome is poor. RNF213 is a ring finger protein and mutation in RNF213 gene is detected in cancers. But the role of RNF213 in glioblastoma is unknown.

methodsRNF213 expression was detected by qPCR, western blotting, IHC technology. RNF213 was overexpressed in plasmid pcDNA3.1. Assays including CCK-8, plate colony formation, wound healing, transwell and FITC/PI dye were used to detect cell behaviors.

resultsRNF213 was shown to express much lower in tumor tissues and in tumor cell lines compared to control. The patients with higher RNF213 expression displayed longer survival time. When RNF213 was overexpressed in U87MG cells, cell proliferation and colony formation were inhibited significantly. The ability of cell migration and invasion was also suppressed. FAC analysis demonstrated that cell apoptosis was increased after RNF213 overexpression. But cell cycle distribution was not affected by RNF213. Then the expression level of MEKK1, JNK, c-Jun, and cdc42 was decreased after RNF213 overexpression, but increased reversely when RNF213 was knocked down by RNAi technology.

conclusionsRNF213 suppresses carcinogenesis and affects MAPK/JNK signaling pathway in glioblastoma. This study suggests that RNF213 might be a promising target for therapy of glioblastoma.

Indexed as

MAP Kinase Signaling SystemMutationAdenosine TriphosphatasesApoptosisBrain NeoplasmsCell Line, TumorCell MovementCell ProliferationGlioblastomaHumansSurvival RateUbiquitin-Protein LigasesAdenosine TriphosphatasesRNF213 protein, humanUbiquitin-Protein LigasesGlioblastomaJNKMAPKRNF213

Identifiers

PMID31953610
OpenAlexW3000236572

What OpenQuestion holds

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Registered trials

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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.