Evidence map›Paper›PMID 36463205›Full record

ArticleCell death & disease2022

The mechanism of BUD13 m6A methylation mediated MBNL1-phosphorylation by CDK12 regulating the vasculogenic mimicry in glioblastoma cells.

Meichen Liu, Xuelei Ruan, Xiaobai Liu, Weiwei Dong, Di Wang, Chunqing Yang, Libo Liu, Ping Wang, Mengyang Zhang, Yixue Xue

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

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  13. Small molecule inhibitors targeting mJournal of hematology & oncology · 2024
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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

10 authors at 2 institutions in 1 country.

Meichen LiuDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China.
Xuelei RuanDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China.
Xiaobai LiuDepartment of Neurosurgery, Shengjing Hospital of China Medical University, 110004, Shenyang, China.
Weiwei DongDepartment of Neurosurgery, Shengjing Hospital of China Medical University, 110004, Shenyang, China.
Di WangDepartment of Neurosurgery, Shengjing Hospital of China Medical University, 110004, Shenyang, China.
Chunqing YangDepartment of Neurosurgery, Shengjing Hospital of China Medical University, 110004, Shenyang, China.
Libo LiuDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China.
Ping WangDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China.
Mengyang ZhangDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China.
Yixue XueDepartment of Neurobiology, School of Life Sciences, China Medical University, 110122, Shenyang, China. xueyixue888@163.com.
China Medical University · CNShenyang Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vasculogenic mimicry (VM) is an endothelium-independent tumor microcirculation that provides adequate blood supply for tumor growth. The presence of VM greatly hinders the treatment of glioblastoma (GBM) with anti-angiogenic drugs. Therefore, targeting VM formation may be a feasible therapeutic strategy for GBM. The research aimed to evaluate the roles of BUD13, CDK12, MBNL1 in regulating VM formation of GBM. BUD13 and CDK12 were upregulated and MBNL1 was downregulated in GBM tissues and cells. Knockdown of BUD13, CDK12, or overexpression of MBNL1 inhibited GBM VM formation. METTL3 enhanced the stability of BUD13 mRNA and upregulated its expression through m6A methylation. BUD13 enhanced the stability of CDK12 mRNA and upregulated its expression. CDK12 phosphorylated MBNL1, thereby regulating VM formation of GBM. The simultaneous knockdown of BUD13, CDK12, and overexpression of MBNL1 reduced the volume of subcutaneously transplanted tumors in nude mice and prolonged the survival period. Thus, the BUD13/CDK12/MBNL1 axis plays a crucial role in regulating VM formation of GBM and provides a potential target for GBM therapy.

Indexed as

Cyclin-Dependent KinasesDNA-Binding ProteinsGlioblastomaMethyltransferasesRNA-Binding ProteinsAnimalsMethylationMiceMice, NudeMicrocirculationNeovascularization, PathologicPhosphorylationRNA, MessengerBud13 protein, mouseCDK12 protein, mouseCyclin-Dependent KinasesDNA-Binding ProteinsMbnl1 protein, mouseMethyltransferasesMettl3 protein, mouseRNA-Binding ProteinsRNA, Messenger

Identifiers

PMID36463205
PMCPMC9719550
OpenAlexW4311216109

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.