Evidence map›Paper›PMID 33483471›Full record

ArticleCell death & disease2021

LINC01152 upregulates MAML2 expression to modulate the progression of glioblastoma multiforme via Notch signaling pathway.

Jianheng Wu, Nannan Wang, Ying Yang, Guangyuan Jiang, Hui Zhan, Fuyong Li

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Mechanistic insights into the lncRNA-Notch signaling axis in tumors.Frontiers in cell and developmental biology · 2026
    Review
  2. Review
  3. Nano-Based Technology in Glioblastoma.Molecules (Basel, Switzerland) · 2025
    Review
  4. Article
  5. Tumor-promoting effect and tumor immunity of SRSFs.Frontiers in cell and developmental biology · 2025
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
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  14. Review
  15. Article
  16. Article
  17. Non-Coding RNAs and Brain Tumors: Insights Into Their Roles in Apoptosis.Frontiers in cell and developmental biology · 2021
    Review
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Jianheng Wu *Department of Neurosurgery, Gaozhou People's Hospital, Gaozhou, 525200, Guangdong, China.
Nannan Wang *Department of Gastroenterology, Gaozhou People's Hospital, Gaozhou, 525200, Guangdong, China.
Ying YangElectroencephalogram Room, Weifang Yidu Central Hospital, Weifang, 262500, Shandong, China.
Guangyuan JiangDepartment of Neurosurgery, Nanxishan Hospital of Guangxi Zhuang Autonomous Region, Guilin, 541000, Guangxi, China.
Hui ZhanDepartment of Neurosurgery, Gaozhou People's Hospital, Gaozhou, 525200, Guangdong, China.
Fuyong LiDepartment of Neurosurgery, the People's Hospital of China Medical University (the People's Hospital of Liaoning Province), Shenyang, 110016, Liaoning, China. Lifuyong126@126.com.
Gaozhou People's Hospital · CNLiaoning Provincial People's Hospital · CNNanxi Mountain Hospital · CNYidu Central Hospital of Weifang · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) brings serious physical and psychological pain to GBM patients, whose survival rate remains not optimistic. Long noncoding RNAs (lncRNAs) have been reported to participate in the progression of many cancers, including GBM. However, the mechanism and function of long intergenic non-protein coding RNA 1152 (LINC01152) in GBM are still unclear. In our study, we aimed to explore the function and mechanism of LINC01152 in GBM. Then qRT-PCR analysis was implemented to search the expression of RNAs in GBM tissues and cells. Functional assays such as EdU assay, colony formation assay, TUNEL assay and flow cytometry analysis were conducted to estimate GBM cell proliferation and apoptosis. RNA pull down assay, luciferase reporter assay, RIP and ChIP assays were implemented to search the binding between molecules. As a result, we discovered that LINC01152 was upregulated in GBM tissues and cells. LINC01152 and mastermind like transcriptional coactivator 2 (MAML2) could both play the oncogenic part in GBM. Moreover, LINC01152 positively regulated MAML2 in GBM by sponging miR-466 and recruiting SRSF1. In turn, RBPJ/MAML2 transcription complex was found to activate the transcription of LINC01152 in GBM cells. In conclusion, LINC01152 could upregulate the expression of MAML2 to promote tumorigenesis in GBM via Notch signaling pathway.

Indexed as

AnimalsBiomarkers, TumorCell Line, TumorDisease ProgressionGlioblastomaHumansMaleMiceMice, NudeNeoplastic Stem CellsSignal TransductionTrans-ActivatorsTransfectionUp-RegulationBiomarkers, TumorMAML2 protein, humanTrans-Activators

Identifiers

PMID33483471
PMCPMC7822850
OpenAlexW3123783665

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.