Evidence map›Paper›PMID 32015336›Full record

ArticleCell death & disease2020

PABPC1-induced stabilization of BDNF-AS inhibits malignant progression of glioblastoma cells through STAU1-mediated decay.

Rui Su, Jun Ma, Jian Zheng, Xiaobai Liu, Yunhui Liu, Xuelei Ruan, Shuyuan Shen, Chunqing Yang, Di Wang, Heng Cai and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 4% 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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 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

12 authors at 1 institution in 1 country.

Rui SuDepartment of Neurobiology, College of Basic Medicine, China Medical University, Shenyang, 110122, China.
Jun MaDepartment of Neurobiology, College of Basic Medicine, China Medical University, Shenyang, 110122, China.
Jian ZhengDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Xiaobai LiuDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Yunhui LiuDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Xuelei RuanDepartment of Neurobiology, College of Basic Medicine, China Medical University, Shenyang, 110122, China.
Shuyuan ShenDepartment of Neurobiology, College of Basic Medicine, China Medical University, Shenyang, 110122, China.
Chunqing YangDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Di WangDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Heng CaiDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Zhen LiDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, 110004, China.
Yixue XueDepartment of Neurobiology, College of Basic Medicine, China Medical University, Shenyang, 110122, China. xueyixue888@163.com.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma is the most common and malignant form of primary central nervous tumor in adults. Long noncoding RNAs (lncRNAs) have been reported to play a pivotal role in modulating gene expression and regulating human tumor's malignant behaviors. In this study, we confirmed that lncRNA brain-derived neurotrophic factor antisense (BDNF-AS) was downregulated in glioblastoma tissues and cells, interacted and stabilized by polyadenylate-binding protein cytoplasmic 1 (PABPC1). Overexpression of BDNF-AS inhibited the proliferation, migration, and invasion, as well as induced the apoptosis of glioblastoma cells. In the in vivo study, PABPC1 overexpression combined with BDNF-AS overexpression produced the smallest tumor and the longest survival. Moreover, BDNF-AS could elicit retina and anterior neural fold homeobox 2 (RAX2) mRNA decay through STAU1-mediated decay (SMD), and thereby regulated the malignant behaviors glioblastoma cells. Knockdown of RAX2 produced tumor-suppressive function in glioblastoma cells and increased the expression of discs large homolog 5 (DLG5), leading to the activation of the Hippo pathway. In general, this study elucidated that the PABPC1-BDNF-AS-RAX2-DLG5 mechanism may contribute to the anticancer potential of glioma cells and may provide potential therapeutic targets for human glioma.

Indexed as

AnimalsApoptosisCell Line, TumorCell MovementCell ProliferationCytoskeletal ProteinsEye ProteinsGene Expression Regulation, NeoplasticGlioblastomaGliomaHomeodomain ProteinsHumansMembrane ProteinsMiceMice, NudePoly(A)-Binding Protein ICytoskeletal ProteinsDLG5 protein, humanEye ProteinsHomeodomain ProteinsMembrane ProteinsPoly(A)-Binding Protein IRAX protein, humanRNA-Binding ProteinsRNA, Long NoncodingSTAU1 protein, humanTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID32015336
PMCPMC6997171
OpenAlexW3004157702

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.