Evidence map›Paper›PMID 30043319›Full record

ArticleJournal of neuro-oncology2018

Blocking LINC00152 suppresses glioblastoma malignancy by impairing mesenchymal phenotype through the miR-612/AKT2/NF-κB pathway.

Jinquan Cai, Jinwei Zhang, Pengfei Wu, Weitong Yang, Qile Ye, Qun Chen, Chuanlu Jiang

Abstract read
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In one paragraph

Article in Journal of neuro-oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

33 citing papers in PubMed, 49 citations in OpenAlex.

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  13. Prognostic and Predictive Biomarkers in Gliomas.International journal of molecular sciences · 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

7 authors at 1 institution in 1 country.

Jinquan CaiDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, No.246, Xuefu Road, Nangang District, Harbin, 150086, China.
Jinwei ZhangDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, No.246, Xuefu Road, Nangang District, Harbin, 150086, China.
Pengfei WuDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, No.246, Xuefu Road, Nangang District, Harbin, 150086, China.
Weitong YangDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, No.246, Xuefu Road, Nangang District, Harbin, 150086, China.
Qile YeDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, No.246, Xuefu Road, Nangang District, Harbin, 150086, China.
Qun ChenDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, No.246, Xuefu Road, Nangang District, Harbin, 150086, China. chenqunmagician@sina.com.
Chuanlu JiangDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, No.246, Xuefu Road, Nangang District, Harbin, 150086, China. jcl6688@163.com.ORCID http://orcid.org/0000-0002-6773-3546
Harbin Medical University · CN

Funding

The Harbin Medical University Scientific Research Innovation Fund 2017LCZX37The Research Project of the Chinese Society of Neuro-oncology, CACA CSNO-2016-MSD12The Research Project of the Health and Family Planning Commission of Heilongjiang Province 2017-201
6 · The paper itself

Abstract

introductionGlioblastoma, the most common and mortal primary brain tumor, accompanied with a dismal clinical outcome in adults. The oncogenic functions of long non-coding RNAs (lncRNAs) in glioblastoma have not been completely illuminated. In the present study, we aimed to investigate the potential role of lncRNA LINC00152 in glioblastoma.

methodsWe used bioinformatic method in public databases to select lncRNA LINC00152 and investigate its clinical value and potential mechanism in glioblastoma. CCK-8, transwell assay, colony formation and wound healing assays were used to explore the role of LINC00152 in glioblastoma malignant behaviors. PCR, western blot, immunofluorescence, reporter assays and nude mouse tumor intracranial model were employed to further verify the regulatory mechanism of LINC00152 in glioblastoma.

resultsLINC00152 was closely associated with glioma WHO classification and poor prognosis, and indicated a poor prognosis in glioblastoma patients. Tumor growth and invasion were suppressed both in vitro and vivo after LINC00152 was blocked. Moreover, LINC00152 modulated GBM malignant progression and proneural-mesenchymal transition through the miR-612 dependent AKT2/NF-κB pathway.

conclusionsLINC00152 acted as a tumor oncogene with prognostic value for patients with glioblastoma through LINC00152/miR-612/AKT2/NF-κB axis.

Indexed as

Biomarkers, TumorBrain NeoplasmsCell Line, TumorComputational BiologyGlioblastomaHumansMesenchymal Stem CellsMicroRNAsNF-kappa BPrognosisProto-Oncogene Proteins c-aktRNA InterferenceRNA, Long NoncodingRNA, Small InterferingSignal TransductionAKT2 protein, humanBiomarkers, Tumorlong non-coding RNA Linc00152, humanMicroRNAsMIRN612 microRNA, humanNF-kappa BProto-Oncogene Proteins c-aktRNA, Long NoncodingRNA, Small InterferingGlioblastomaLINC00152MiR-612NF-κBProneural–mesenchymal transition

Identifiers

PMID30043319
OpenAlexW2883686572

What OpenQuestion holds

Textmetadata
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.