Evidence map›Paper›PMID 36114444›Full record

ArticleBMC neuroscience2022

A circular RNA derived from GLIS3 accelerates the proliferation of glioblastoma cells through competitively binding with miR-449c-5p to upregulate CAPG and GLIS3.

Qingjiu Zhou, Mahati Shaya, Yalikun Kugeluke, Qiang Fu, Shaoshan Li, Yisireyili Dilimulati

Open access · goldAbstract read
In one paragraph

Article in BMC neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. METTL3-mediated mCellular & molecular biology letters · 2024
    Article
  5. The Glioblastoma CircularRNAome.International journal of molecular sciences · 2023
    Review
  6. Review
  7. Review
  8. Review
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.

Qingjiu ZhouDepartment of Neurosurgery, The First Affiliated Hospital of Xinjiang Medical University, No.137 South Liyushan Road, Ürümqi, 830054, Xinjiang, China. zhouqingjiu007@163.com.
Mahati ShayaDepartment of Oncology, The First Affiliated Hospital of Xinjiang Medical University, Ürümqi, 830054, Xinjiang, China.
Yalikun KugelukeDepartment of Neurosurgery, Yili Friendship Hospital, Yili, 835000, Xinjiang, China.
Qiang FuDepartment of Neurosurgery, The First Affiliated Hospital of Xinjiang Medical University, No.137 South Liyushan Road, Ürümqi, 830054, Xinjiang, China.
Shaoshan LiDepartment of Neurosurgery, The First Affiliated Hospital of Xinjiang Medical University, No.137 South Liyushan Road, Ürümqi, 830054, Xinjiang, China.
Yisireyili DilimulatiDepartment of Neurosurgery, The First Affiliated Hospital of Xinjiang Medical University, No.137 South Liyushan Road, Ürümqi, 830054, Xinjiang, China.
Xinjiang Medical University · CNFirst Affiliated Hospital of Xinjiang Medical University · CNYili Friendship Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlioblastoma (GBM) is an aggressive and malignant brain tumor with extremely poor prognosis. Despite advances in treatment, the pathogenesis of GBM remains elusive. Mounting studies have revealed the critical role of circular RNAs (circRNAs) in the development and progression of human cancers including GBM, but the comprehension of their functions is still insufficient. In this study, we investigated the expression profile of a circRNA derived from GLIS family zinc finger 3 (GLIS3) in GBM and normal astrocytes. CircGLIS3 expression was detected through quantitative real-time polymerase chain reaction (qRT-PCR) analysis. Functional experiments were performed to analyze the influence of circGLIS3 on GBM cell proliferation and apoptosis. In addition, mechanism assays were to uncover the potential regulatory mechanism of circGLIS3.

resultsCircGLIS3 was up-regulated in GBM cells and knockdown of circGLIS3 significantly hampered proliferation and promoted apoptosis of GBM cells. Furthermore, circGLIS3 positively regulated CAPG and GLIS3 by sponging miR-449c-5p to affect GBM cell proliferation and apoptosis.

conclusionsIn summary, our study identified that circGLIS3 could promote proliferation and inhibit apoptosis of GBM cells via targeting miR-449c-5p/GLIS3/CAPG axis in vitro. This study could offer a novel molecular perspective for further investigation into mechanisms essential to GBM progression.

Indexed as

Brain NeoplasmsGlioblastomaMicroRNAsRNA, CircularCell ProliferationDNA-Binding ProteinsHumansMicrofilament ProteinsNuclear ProteinsRepressor ProteinsTrans-ActivatorsCAPG protein, humanDNA-Binding ProteinsGLIS3 protein, humanMicrofilament ProteinsMicroRNAsNuclear ProteinsRepressor ProteinsRNA, CircularTrans-ActivatorsCAPGcircGLIS3GlioblastomaGLIS3miR-449c-5p

Identifiers

PMID36114444
PMCPMC9479268
OpenAlexW4296041791

What OpenQuestion holds

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LicenceCC BY
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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.