Evidence map›Paper›PMID 36203070›Full record

ArticleIn vitro cellular & developmental biology. Animal2022

TRIM47 promotes glioma angiogenesis by suppressing Smad4.

Zifan Wang, Zhiqiang Li, Chuangchuang Han, Yuanchi Cheng, Kaimin Wang

Abstract read
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In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Roles of the E3 Ubiquitin Ligase TRIM47 in Inflammation, Organ Injury, and Cancer.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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.

Zifan Wang *The Affiliated Fengxian Hospital, The Central Hospital of Fengxian District) of Anhui University of Science & Technology, Shanghai Neurological Research Institute of Anhui University of Science & Technology, Shanghai, 201400, China.
Zhiqiang Li *Department of Neurosurgery, The Central Hospital of Fengxian District (Shanghai Neurological Research Institute of Anhui University of Science & Technology, The Affiliated Hospital of Anhui University of Science & Technology), 6600 Nanfeng Road, Shanghai, 201400, China.
Chuangchuang HanThe Affiliated Fengxian Hospital, The Central Hospital of Fengxian District) of Anhui University of Science & Technology, Shanghai Neurological Research Institute of Anhui University of Science & Technology, Shanghai, 201400, China.
Yuanchi ChengDepartment of Neurosurgery, The Central Hospital of Fengxian District (Shanghai Neurological Research Institute of Anhui University of Science & Technology, The Affiliated Hospital of Anhui University of Science & Technology), 6600 Nanfeng Road, Shanghai, 201400, China.
Kaimin WangDepartment of Neurosurgery, The Central Hospital of Fengxian District (Shanghai Neurological Research Institute of Anhui University of Science & Technology, The Affiliated Hospital of Anhui University of Science & Technology), 6600 Nanfeng Road, Shanghai, 201400, China. Celinda666@163.com.ORCID http://orcid.org/0000-0002-8290-9159
Anhui University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiogenesis is required for tumor progression; thus, its investigation can be useful to identify strategies for potential cancer treatments. Tripartite motif 47 (TRIM47) is involved in the progression of multiple cancers. However, its role in glioma angiogenesis is largely unknown. In this study, we first showed that TRIM47 is frequently upregulated in gliomas, and increased TRIM47 levels are correlated with microvascular density. We then examined the role of TRIM47 in cellular functions related to angiogenesis in vitro and observed that TRIM47 knockdown significantly reduced human umbilical vein endothelial cell proliferation, migration, and tube formation. We also found that TRIM47 silencing reduced vessel density and tumor volume in glioma xenografts. Mechanistically, TRIM47 negatively regulated Smad4 expression in glioma cells, and SMAD4 knockdown rescued the suppressive effects of TRIM47 silencing. Taken together, our results indicate that TRIM47 promotes angiogenesis in gliomas by downregulating SMAD4. Therefore, targeting the TRIM47/SMAD4 axis may offer an innovative approach to glioma treatment.

Indexed as

GliomaAnimalsCarrier ProteinsCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansHuman Umbilical Vein Endothelial CellsNeoplasm ProteinsNeovascularization, PathologicNuclear ProteinsSmad4 ProteinTripartite Motif ProteinsCarrier ProteinsNeoplasm ProteinsNuclear ProteinsSmad4 ProteinSMAD4 protein, humanTRIM47 protein, humanTripartite Motif ProteinsAngiogenesisGliomaSMAD4TRIM47

Identifiers

PMID36203070
OpenAlexW4302362766

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.