Evidence map›Paper›PMID 29577647›Full record

ArticleCNS neuroscience & therapeutics2018

Long noncoding RNA LINC00152 is a potential prognostic biomarker in patients with high-grade glioma.

Wen Wang, Fan Wu, Zheng Zhao, Kuan-Yu Wang, Ruo-Yu Huang, Hao-Yuan Wang, Qing Lan, Jiang-Fei Wang, Ji-Zong Zhao

Open access · bronzeAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2018. 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
1.4field-weighted citation impact, top 23% 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, 30 citations in OpenAlex.

  1. Review
  2. Targeting LINC00152 activates cAMP/CaCell death & disease · 2024
    Article
  3. Targeting LINC00152 activates cAMP/CabioRxiv : the preprint server for biology · 2023
    Article
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  15. Role of LINC00152 in non-small cell lung cancer.Journal of Zhejiang University. Science. B
    Article
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 3 institutions in 1 country.

Wen WangDepartment of Neurosurgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Fan WuChinese Glioma Cooperative Group (CGCG), Beijing, China.
Zheng ZhaoChinese Glioma Cooperative Group (CGCG), Beijing, China.
Kuan-Yu WangChinese Glioma Cooperative Group (CGCG), Beijing, China.
Ruo-Yu HuangChinese Glioma Cooperative Group (CGCG), Beijing, China.
Hao-Yuan WangChinese Glioma Cooperative Group (CGCG), Beijing, China.
Qing LanDepartment of Neurosurgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Jiang-Fei WangDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Ji-Zong ZhaoDepartment of Neurosurgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.ORCID 0000-0002-1269-0972
Capital Medical University · CNAnhui Medical University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsTo investigate the role of LINC00152 in high-grade glioma (HGG).

methodsWe collected data from the Chinese Glioma Genome Atlas (CGGA) microarray, CGGA RNA sequencing, and GSE16011 datasets to evaluate the expression and prognostic relationship of LINC00152 in patients with HGGs. A knockdown assay was performed to determine the function of LINC00152 in glioma development and progression in vitro and in vivo.

resultsThe expression of LINC00152 was increased with glioma grade, especially in the mesenchymal TCGA subtype. LINC00152 was independently associated with poor prognosis, and the overall survival (OS) of the high expression group was shorter than the low expression group (median OS 14.77 vs 9.65 months; P = 0.0216) in the CGGA microarray dataset. The results were validated in the other 2 datasets. Based on the expression of LINC00152, 4288 (2519 positively; 1769 negatively) probes were extracted to perform a biological process analysis using the Database for Annotation, Visualization, and Integrated Discovery. Positively regulated genes were enriched in immune response, apoptotic process, cell adhesion, and regulation of cell proliferation. The clinical and molecular features of HGG patients indicated that patients in the LINC00152 high expression group tended to display the mesenchymal type, older (≥46 years), isocitrate dehydrogenase1 wild-type, O(6)-methylguanine DNA methyltransferase unmethylated, nonchemotherapy, and low karnofsky performance status. Functionally, knockdown of LINC00152 inhibited cell proliferation, migration, and invasion and increased the sensitivity of chemotherapy in vitro.

conclusionOur results indicate that knockdown of LINC00152 could inhibit tumor growth in vivo. LINC00152 could serve as a potential prognostic biomarker in patients with HGG.

Indexed as

AnimalsBrain NeoplasmsCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticGliomaHumansKaplan-Meier EstimateMaleMice, NudeMicroarray AnalysisNeoplasm InvasivenessPrognosisProportional Hazards Modelslong non-coding RNA Linc00152, humanRNA, Long NoncodingRNA, Small InterferinggliomaLINC00152long noncoding RNAmicroarrayRNA sequencing

Identifiers

PMID29577647
PMCPMC6489806
OpenAlexW2792373310

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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.