Evidence map›Paper›PMID 34716872›Full record

ArticleHuman cell2022

LncRNA LINC01094 contributes to glioma progression by modulating miR-224-5p/CHSY1 axis.

Luotong Liu, Qian Xu, Yu Xiong, Huajiang Deng, Jie Zhou

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 29% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
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  7. Review
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  9. Article
  10. LINCRNA01094 Promotes Renal Interstitial Fibrosis via the Mir-513b-5p/ MELK/Smad3 Axis.Endocrine, metabolic & immune disorders drug targets · 2025
    Article
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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

5 authors at 1 institution in 1 country.

Luotong LiuDepartment of Neurosurgery, Affiliated Hospital of Southwest Medical University, Luzhou, China.
Qian XuDepartment of Neurosurgery, Affiliated Hospital of Southwest Medical University, Luzhou, China.
Yu XiongDepartment of Neurosurgery, Affiliated Hospital of Southwest Medical University, Luzhou, China.
Huajiang DengDepartment of Neurosurgery, Affiliated Hospital of Southwest Medical University, Luzhou, China.
Jie ZhouDepartment of Neurosurgery, Affiliated Hospital of Southwest Medical University, Luzhou, China. rose810206@sina.com.
Affiliated Hospital of Southwest Medical University · CN

Funding

Sichuan Provincial Science and Technology Department Project 2018JY0403Technology and Human resources' Bureau of Luzhou 17256Youth innovative Scientific Research Project of Sichuan Medical Association Q16076
6 · The paper itself

Abstract

Glioma serves as the most common malignancy influencing modern people and is associated with severe morbidity and high mortality. Long non-coding RNAs (lncRNAs) as crucial regulators participate in multiple cancer progression. However, the role of lncRNA LINC01094 in the development of glioma remains unclear. Here, we aimed to explore the effect of lncRNA LINC01094 on the glioma progression and the underlying mechanism. Significantly, we revealed that the expression levels of LINC01094 were elevated in the glioma patient tissues compared to adjacent normal tissues. The LINC01094 expression was enhanced in the glioma cell lines. The depletion of LINC01094 inhibited cell viability and colony formation in the glioma cells. Meanwhile, the migration and invasion of glioma cells were impaired by the depletion of LINC01094. Mechanically, we identified that LINC01094 was able to sponge the miR-224-5p in the glioma cells and miR-224-5p inhibitor could reverse the effect of LINC01094 on glioma progression. In addition, miR-224-5p targeted CHSY1 and LINC01094 up-regulated CHSY1 by targeting miR-224-5p in the glioma cells. LINC01094 promoted glioma progression by the positive regulation of CHSY1. Moreover, tumorigenicity analysis showed that LINC01094 enhanced tumor growth of glioma in vivo. Thus, we conclude that lncRNA LINC01094 promotes glioma progression by modulating miR-224-5p/CHSY1 axis. Our finding provides new insights into the mechanism by which lncRNA LINC01094 contributes to the development of glioma, improving the understanding of lncRNA LINC01094 and glioma. LncRNA LINC01094, miR-224-5p, and CHSY1 may serve as potential targets for glioma.

Indexed as

Gene ExpressionAnimalsBrain NeoplasmsCarcinogenesisCell Line, TumorCell SurvivalDisease ProgressionGene Expression Regulation, NeoplasticGliomaGlucuronosyltransferaseHumansMiceMice, NudeMicroRNAsMolecular Targeted TherapyMultifunctional EnzymesCHSY1 protein, humanGlucuronosyltransferaseMicroRNAsMIRN224 microRNA, humanMultifunctional EnzymesN-AcetylgalactosaminyltransferasesRNA, Long NoncodingCHSY1GliomaLncRNA LINC01094MiR-224-5pProgression

Identifiers

PMID34716872
OpenAlexW3208778134

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.