Evidence map›Paper›PMID 33078370›Full record

ArticleMolecular neurobiology2021

Long Non-coding RNA MALAT1 Upregulates ZEB2 Expression to Promote Malignant Progression of Glioma by Attenuating miR-124.

Hongyu Cheng, Haikang Zhao, Xin Xiao, Qian Huang, Wen Zeng, Bo Tian, Tao Ma, Dan Lu, Yulong Jin, Yuqian Li

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

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  7. Crosstalk betweenInternational journal of molecular sciences · 2023
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  14. Unveiling a Ghost Proteome in the Glioblastoma Non-Coding RNAs.Frontiers in cell and developmental biology · 2021
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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

10 authors at 5 institutions in 1 country.

Hongyu Cheng *Department of Ultrasound Diagnosis, Tangdu Hospital, Air Force Medical University, No.1, Xinsi Road, Xi'an, 710038, Shaanxi, China.
Haikang Zhao *Department of Neurosurgery, The Second Hospital Affiliated of Xi'an Medical University, Xi'an, Shaanxi, China.
Xin Xiao *Department of Orthopedics, Xijing Hospital, Air Force Medical University, Xi'an, Shaanxi, China.
Qian HuangCollege of Basic Medicine, Air Force Medical University, Xi'an, Shaanxi, China.
Wen ZengDepartment of Neurosurgery, Tangdu Hospital, Air Force Medical University, Xi'an, Shaanxi, China.
Bo TianDepartment of Neurosurgery, Tangdu Hospital, Air Force Medical University, Xi'an, Shaanxi, China.
Tao MaDepartment of Neurosurgery, Tangdu Hospital, Air Force Medical University, Xi'an, Shaanxi, China.
Dan LuDepartment of Neurosurgery, Tangdu Hospital, Air Force Medical University, Xi'an, Shaanxi, China.
Yulong JinDepartment of Hematology, General Hospital of Central Theater Command, Wuhan, 430030, Hubei, China. 468104986@qq.com.
Yuqian LiDepartment of Neurosurgery, Tangdu Hospital, Air Force Medical University, Xi'an, Shaanxi, China. liyuqiancheng@126.com.ORCID http://orcid.org/0000-0002-3164-6248
Air Force Medical University · CNCentral Hospital of Wuhan · CNTang Du Hospital · CNXi'an Medical University · CNXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNA (lncRNA) metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) has been shown to play a critical role in the development of several malignancies. However, the potential molecular mechanism of MALAT1 in glioma remains unclear. In the present study, we found that the expression of MALAT1 was aberrantly increased in both human glioma tissues and cells and associated with poor prognosis in glioma patients. We further found that MALAT1 silencing significantly inhibited glioma cell proliferation while induced cell cycle arrest and apoptosis. In parallel, knockdown of MALAT1 decreased tumor volume in vivo. These results suggested that MALAT1 acts as a functional oncogene, resulting in the oncogenicity in glioma. Nevertheless, the tumor-suppressive effect of MALAT1 silencing was reversed by miR-124. Besides, the relevance of ZEB2 in tumor progression has been studied in several forms of human cancer, and ZEB2 was identified as a target of miR-124 and negatively regulated by miR-124. MALAT1 overexpression or miR-124 inhibitor led to increased expression of ZEB2. In summary, our study depicts a novel pathway of MALAT1/miR-124/ZEB2 that regulates the progression of glioma and might provide a promising strategy for glioma therapy.

Indexed as

Disease ProgressionAnimalsApoptosisBase SequenceBrain NeoplasmsCarcinogenesisCell Cycle CheckpointsCell Line, TumorCell ProliferationDown-RegulationGene Expression Regulation, NeoplasticGliomaHumansMiceMice, Inbred BALB CMice, NudeMALAT1 long non-coding RNA, humanMicroRNAsMIRN124 microRNA, humanRNA, Long NoncodingZEB2 protein, humanZinc Finger E-box Binding Homeobox 2GliomaLncRNAMALAT1miR-124ZEB2

Identifiers

PMID33078370
OpenAlexW3093025902

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.