Evidence map›Paper›PMID 32918360›Full record

ArticleJournal of cellular and molecular medicine2020

LncRNA HOXA-AS3 promotes the malignancy of glioblastoma through regulating miR-455-5p/USP3 axis.

Wanghao Chen, Qiaoyu Li, Guilong Zhang, Hong Wang, Zhihan Zhu, Lukui Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.1field-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

31 citing papers in PubMed, 62 citations in OpenAlex.

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  14. Biomaterial-basedCancer pathogenesis and therapy · 2023
    Review
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  18. The Characterization and Differential Analysis of mAnimals : an open access journal from MDPI · 2023
    Article
  19. The integrated comprehension of lncRNA HOXA-AS3 implication on human diseases.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  20. 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

6 authors at 3 institutions in 1 country.

Wanghao ChenMedical School of Southeast University, Nanjing, China.ORCID 0000-0001-8376-8901
Qiaoyu LiDepartment of Neurosurgery, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.ORCID 0000-0001-6123-6074
Guilong ZhangMedical School of Southeast University, Nanjing, China.ORCID 0000-0001-5367-1535
Hong WangMedical School of Southeast University, Nanjing, China.
Zhihan ZhuMedical School of Southeast University, Nanjing, China.ORCID 0000-0003-0694-5227
Lukui ChenMedical School of Southeast University, Nanjing, China.ORCID 0000-0002-8075-8369
Southeast University · CNJiangsu University · CNTCM-Intigrated Cancer Center of Southern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our objective was to determine the molecular mechanisms by which lncRNA HOXA-AS3 regulates the biological behaviour of glioblastoma multiforme (GBM). We used an lncRNA microarray assay to identify GBM-related lncRNA expression profiles. Qrt-PCR was used to survey the levels of expression of long non-coding RNA (lncRNA) HOXA-AS3 and the target gene. Dual-luciferase reporter assays were used to investigate the interaction of lncRNA HOXA-AS3, the target gene and miRNA. Western blot analysis was used to examine the expression of USP3 and epithelial-mesenchymal transition (EMT) genes. The MTT assay, transwell assay and wound healing assay were used to analyse the effects of lncRNA HOXA-AS3 on GBM cell viability, mobility and invasiveness, respectively. Our results showed that lncRNA HOXA-AS3 was significantly up-regulated in GBM cells and could promote GBM cell proliferation, invasion and migration in vitro and in vivo. HOXA-AS was found to be associated with poor survival prognosis in glioma patients. The dual-luciferase reporter assay also revealed that lncRNA HOXA-AS3 acts as a mir-455-5p sponge by up-regulating USP3 expression to promote GBM progression. Western blot analysis showed that lncRNA HOXA-AS3 could up-regulate EMT-related gene expression in GBM. Experiments showed mir-455-5p could rescue the effect of lncRNA HOXA-AS3 on cell proliferation and invasion. The newly identified HOXA-AS3/mir-455-5p/USP3 pathway offers important clues to understanding the key mechanisms underlying the action of lncRNA HOXA-AS3 in glioblastoma.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBase SequenceBrain NeoplasmsCarcinogenesisCell Line, TumorCell ProliferationEpithelial-Mesenchymal TransitionGlioblastomaHumansMice, NudeMicroRNAsNeoplasm InvasivenessRNA, Long NoncodingUbiquitin-Specific ProteasesUp-RegulationMicroRNAsMIRN455 microRNA, humanRNA, Long NoncodingUbiquitin-Specific ProteasesUSP3 protein, humancompeting endogenous RNAglioblastomalncRNA HOXA-AS3miR-455-5pUSP3

Identifiers

PMID32918360
PMCPMC7579690
OpenAlexW3085343430

What OpenQuestion holds

Textmetadata
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.