Evidence map›Paper›PMID 36359873›Full record

ArticleCells2022

Visfatin-Induced Inhibition of miR-1264 Facilitates PDGF-C Synthesis in Chondrosarcoma Cells and Enhances Endothelial Progenitor Cell Angiogenesis.

Chang-Yu Song, Sunny Li-Yun Chang, Chih-Yang Lin, Chun-Hao Tsai, Shang-Yu Yang, Yi-Chin Fong, Yu-Wen Huang, Shih-Wei Wang, Wei-Cheng Chen, Chih-Hsin Tang

Open access · goldAbstract read
In one paragraph

Article in Cells, 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
1.0field-weighted citation impact, top 25% 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, 13 citations in OpenAlex.

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  7. Genetic associations ofInternational journal of medical sciences · 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 4 institutions in 1 country.

Chang-Yu SongGraduate Institute of Biomedical Science, China Medical University, Taichung 404333, Taiwan.
Sunny Li-Yun ChangGraduate Institute of Biomedical Science, China Medical University, Taichung 404333, Taiwan.
Chih-Yang LinGraduate Institute of Biomedical Science, China Medical University, Taichung 404333, Taiwan.
Chun-Hao TsaiDepartment of Sports Medicine, College of Health Care, China Medical University, Taichung 404333, Taiwan.ORCID 0000-0002-4428-3132
Shang-Yu YangDepartment of Healthcare Administration, College of Medical and Health Science, Asia University, Taichung 400354, Taiwan.ORCID 0000-0001-6690-7420
Yi-Chin FongDepartment of Sports Medicine, College of Health Care, China Medical University, Taichung 404333, Taiwan.
Yu-Wen HuangGraduate Institute of Biomedical Science, China Medical University, Taichung 404333, Taiwan.
Shih-Wei WangDepartment of Medicine, MacKay Medical College, New Taipei City 25245, Taiwan.ORCID 0000-0001-7522-6352
Wei-Cheng ChenDepartment of Medicine, MacKay Medical College, New Taipei City 25245, Taiwan.
Chih-Hsin TangGraduate Institute of Biomedical Science, China Medical University, Taichung 404333, Taiwan.ORCID 0000-0002-7113-8352
China Medical University · TWAsia University · TWMackay Medical University · TWMackay Memorial Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New treatments for chondrosarcoma are extremely important. Chondrosarcoma is a primary malignant bone tumor with a very unfavorable prognosis. High-grade chondrosarcoma has a high potential to metastasize to any organ in the body. Platelet-derived growth factor (PDGF) is a potent angiogenic factor that promotes tumor angiogenesis and metastasis. The adipocytokine visfatin promotes metastatic potential of chondrosarcoma; however, the role of visfatin in angiogenesis in human chondrosarcoma is unclear. We report that the levels of PDGF-C expression were positively correlated with tumor stages, significantly higher than the levels of expression in normal cartilage. Visfatin increased PDGF-C expression and endothelial progenitor cell (EPC) angiogenesis through the PI3K/Akt/mTOR signaling pathway, and dose-dependently down-regulated the synthesis of miR-1264, which targets the 3'-UTR of PDGF-C. Additionally, we discovered inhibition of visfatin or PDGF-C in chondrosarcoma tumors significantly reduced tumor angiogenesis and size. Our results indicate that visfatin inhibits miR-1264 production through the PI3K/Akt/mTOR signaling cascade, and thereby promotes PDGF-C expression and chondrosarcoma angiogenesis. Visfatin may be worth targeting in the treatment of chondrosarcoma angiogenesis.

Indexed as

Bone NeoplasmsChondrosarcomaEndothelial Progenitor CellsMicroRNAsHumansLymphokinesNeovascularization, PathologicNicotinamide PhosphoribosyltransferasePhosphatidylinositol 3-KinasesPlatelet-Derived Growth FactorProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesVascular Endothelial Growth Factor ALymphokinesMicroRNAsNicotinamide PhosphoribosyltransferasePhosphatidylinositol 3-KinasesPlatelet-Derived Growth Factorplatelet-derived growth factor CProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesVascular Endothelial Growth Factor Aangiogenesischondrosarcomaendothelial progenitor cellPDGF-Cplatelet-derived growth factortumor angiogenesisvisfatin

Identifiers

PMID36359873
PMCPMC9656973
OpenAlexW4309091523

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.