Evidence map›Paper›PMID 34106407›Full record

ArticleJournal of molecular neuroscience : MN2021

An E3 Ubiquitin Ligase RNF139 Serves as a Tumor-Suppressor in Glioma.

Xiaofeng Chen, Weiping Kuang, Yong Zhu, Bin Zhou, Xiaosong Li, Xi Zhang, Bo Li, Liang Li, Shucheng Zou

Open access · hybridAbstract read
In one paragraph

Article in Journal of molecular neuroscience : MN, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

4 citing papers in PubMed, 5 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 2 institutions in 1 country.

Xiaofeng ChenDepartment of Neurosurgery, Hunan Brain Hospital, Clinical Medical School of Hunan, University of Chinese Medicine, Changsha, 410007, Hunan Province, China.
Weiping KuangDepartment of Neurosurgery, Hunan Brain Hospital, Clinical Medical School of Hunan, University of Chinese Medicine, Changsha, 410007, Hunan Province, China.
Yong ZhuDepartment of Neurosurgery, Hunan Brain Hospital, Clinical Medical School of Hunan, University of Chinese Medicine, Changsha, 410007, Hunan Province, China.
Bin ZhouDepartment of Neurosurgery, Hunan Brain Hospital, Clinical Medical School of Hunan, University of Chinese Medicine, Changsha, 410007, Hunan Province, China.
Xiaosong LiDepartment of Neurosurgery, Hunan Brain Hospital, Clinical Medical School of Hunan, University of Chinese Medicine, Changsha, 410007, Hunan Province, China.
Xi ZhangDepartment of Neurosurgery, Hunan Brain Hospital, Clinical Medical School of Hunan, University of Chinese Medicine, Changsha, 410007, Hunan Province, China.
Bo LiDepartment of Neurosurgery, Hunan Brain Hospital, Clinical Medical School of Hunan, University of Chinese Medicine, Changsha, 410007, Hunan Province, China.
Liang LiDepartment of Neurosurgery, Hunan Brain Hospital, Clinical Medical School of Hunan, University of Chinese Medicine, Changsha, 410007, Hunan Province, China. superliliang@126.com.ORCID http://orcid.org/0000-0001-9994-4690
Shucheng ZouDepartment of Neurosurgery, Hunan Brain Hospital, Clinical Medical School of Hunan, University of Chinese Medicine, Changsha, 410007, Hunan Province, China. 2297128086@qq.com.
Hunan University · CNHunan University of Traditional Chinese Medicine · CN

Funding

Hunan Province Science and technology innovation plan project 2018SK50605Hunan Provincial Health and Family Planning Commission Project C2019043Hunan Science and technology major special program 2018SK1030Natural Science Foundation of Hunan Province 2019JJ80024Natural Science Foundation of Hunan Province 2020JJ8081
6 · The paper itself

Abstract

Glioma is highly lethal because of its high malignancy. Ubiquitination, a type of ubiquitin-dependent protein modification, has been reported to play an oncogenic or tumor-suppressive role in glioma development, depending on the targets. Ring finger protein 139 (RNF139) is a membrane-bound E3 ubiquitin ligase serving as a tumor suppressor by ubiquitylation-dependently suppressing cell growth. Herein, we firstly confirmed the abnormal downregulation of RNF139 in glioma tissues and cell lines. In glioma cells, ectopic RNF139 overexpression could inhibit, whereas RNF139 knockdown could aggravate the aggressive behaviors of glioma cells, including hyperproliferation, migration, and invasion. Moreover, in two glioma cell lines, RNF139 overexpression inhibited, whereas RNF139 knockdown enhanced the phosphorylation of phosphatidylinositol 3-kinase (PI3K) and AKT serine/threonine kinase 1 (AKT). In a word, we demonstrate the aberration in RNF139 expression in glioma tissue samples and cell lines. RNF139 serves as a tumor-suppressor in glioma by inhibiting glioma cell proliferation, migration, and invasion and promoting glioma cell apoptosis through regulating PI3K/AKT signaling.

Indexed as

Brain NeoplasmsCell Line, TumorCell ProliferationGenes, Tumor SuppressorGliomaHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptors, Cell SurfaceSignal TransductionPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptors, Cell SurfaceRNF139 protein, humanE3 ubiquitin ligaseGliomaRNF139The PI3K/AKT signaling

Identifiers

PMID34106407
PMCPMC8349318
OpenAlexW3172441483

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.