Evidence map›Paper›PMID 33057597›Full record

Observational studyBioscience reports2020

LncRNA NEAT1 promotes malignant phenotypes and TMZ resistance in glioblastoma stem cells by regulating let-7g-5p/MAP3K1 axis.

Chang-Long Bi, Jin-Fang Liu, Ming-Yu Zhang, Song Lan, Zhuan-Yi Yang, Jia-Sheng Fang

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

28 citing papers in PubMed, 36 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

6 authors at 1 institution in 1 country.

Chang-Long BiDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, P.R. China.
Jin-Fang LiuDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, P.R. China.
Ming-Yu ZhangDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, P.R. China.
Song LanDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, P.R. China.
Zhuan-Yi YangDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, P.R. China.
Jia-Sheng FangDepartment of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, P.R. China.
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is one of the most malign brain tumors in adults. Temozolomide (TMZ) is an oral chemotherapy drug constituting the backbone of chemotherapy regimens utilized as first-line treatment of GBM. However, resistance to TMZ often leads to treatment failure. In the present study, we explored the expression and related mechanisms of nuclear enriched abundant transcript 1 (NEAT1) in glioma stem cells (GSCs). Quantitative real-time PCR (qRT-PCR) showed that NEAT1 was up-regulated in serum samples of GBM patients and GSCs isolated from U87, U251 cell lines. Functional experiments showed that NEAT1 knockdown restrained malignant behaviors of GSC, including proliferation, migration and invasion. Dual-luciferase assays identified let-7g-5p was a downstream target and negatively adjusted by NEAT1. Restoration of let-7g-5p impeded tumor progression by inhibiting proliferation, migration and invasion. Mitogen-activated protein kinase kinase kinase 1 (MAP3K1), as a direct target of let-7g-5p, was positively regulated by NEAT1 and involved to affect the regulation of NEAT1 on GSCs' behaviors. In conclusion, our results suggested that NEAT1 promoted GSCs progression via NEAT1/let-7g-5p/MAP3K1 axis, which provided a depth insight into TMZ resistance mechanism.

Indexed as

Brain NeoplasmsCase-Control StudiesCell Line, TumorCell MovementCell ProliferationDrug Resistance, NeoplasmGene Knockdown TechniquesGlioblastomaHealthy VolunteersHumansMAP Kinase Kinase Kinase 1MicroRNAsNeoplasm InvasivenessNeoplastic Stem CellsRNA, Long NoncodingTemozolomideMAP3K1 protein, humanMAP Kinase Kinase Kinase 1MicroRNAsmirnlet7 microRNA, humanNEAT1 long non-coding RNA, humanRNA, Long NoncodingTemozolomideGlioma stem cellslet-7g-5plncRNAMAP3K1NEAT1Temozolomide

Identifiers

PMID33057597
PMCPMC7601351
OpenAlexW3093138698

What OpenQuestion holds

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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.