Evidence map›Paper›PMID 37893141›Full record

ArticleBiomedicines2023

Chemokine Ligand 2 Promotes Migration in Osteosarcoma by Regulating the miR-3659/MMP-3 Axis.

Yu-Hsiang Chang, Yuan-Li Huang, Hsiao-Chi Tsai, An-Chen Chang, Chih-Yuan Ko, Yi-Chin Fong, Chih-Hsin Tang

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-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

7 citing papers in PubMed, 6 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Yu-Hsiang ChangProgram for Cancer Biology and Drug Discovery, China Medical University, Taichung 404328, Taiwan.
Yuan-Li HuangDepartment of Medical Laboratory Science and Biotechnology, Asia University, Taichung 41354, Taiwan.ORCID 0000-0002-3405-8863
Hsiao-Chi TsaiDepartment of Medical Education and Research, China Medical University Beigang Hospital, Yunlin 651012, Taiwan.
An-Chen ChangTranslational Medicine Center, Shin-Kong Wu Ho-Su Memorial Hospital, Taipei 111045, Taiwan.
Chih-Yuan KoGraduate Institute of Biomedical Sciences, China Medical University, Taichung 404328, Taiwan.ORCID 0000-0001-7752-2833
Yi-Chin FongDepartment of Orthopedic Surgery, China Medical University Hospital, Taichung 404327, Taiwan.
Chih-Hsin TangProgram for Cancer Biology and Drug Discovery, China Medical University, Taichung 404328, Taiwan.ORCID 0000-0002-7113-8352
China Medical University · TWAsia University · TW

Funding

Chih-Yuan KO CMU112-ASIA-10Chun-Hao Tsai CMU112-ASIA-05Chun-Hao Tsai DMR-111-117Chun-Hao Tsai DMR-112-091Yi-Chin Fong DMR-112-090Yi-Chin Fong MOST 111-2314-B-039-048-MY3
6 · The paper itself

Abstract

Osteosarcoma is a common malignant tumor in children and adolescents, known for its aggressive invasion and distant metastasis, leading to a poor prognosis. Matrix metalloproteinases (MMPs) can degrade the extracellular matrix and basement membranes through their proteolytic activity, thereby promoting osteosarcoma metastasis. Chemokine ligand 2 (CCL2) is a well-studied chemokine that plays a significant role in the cell motility of many cancers. However, its specific involvement in osteosarcoma metastasis is not fully understood. The aim of this study is to examine the role of miRNAs in CCL2-mediated MMP expression and cell motility in human osteosarcoma. The analysis of immunohistochemistry data and databases associated a positive correlation between CCL2 or MMP-3 levels with the metastasis of osteosarcoma patients. The in vivo lung metastatic osteosarcoma model also demonstrated similar effects, showing higher levels of CCL2 and MMP-3 in lung metastatic osteosarcoma tissues. The stimulation of osteosarcoma cells with CCL2 enhanced migration and invasion abilities through the upregulation of MMP-3 synthesis. Our results also indicate that CCL2 enhances MMP-3-dependent cell motility by inhibiting miR-3659 synthesis. Therefore, CCL2 represents a promising therapeutic target for treating metastasis in osteosarcoma.

Indexed as

CCL2metastasismiR-3659MMP-3osteosarcoma

Identifiers

PMID37893141
PMCPMC10604484
OpenAlexW4387568421

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.