Evidence map›Paper›PMID 29628305›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2018

miR-223-3p Inhibits Human Osteosarcoma Metastasis and Progression by Directly Targeting CDH6.

Quanbo Ji, Xiaojie Xu, Qi Song, Yameng Xu, Yanhong Tai, Stuart B Goodman, Wenzhi Bi, Meng Xu, Shunchang Jiao, William J Maloney and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 2% 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

75 citing papers in PubMed, 1 synthesis or guideline pooled it, 119 citations in OpenAlex.

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  12. MiRZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
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15 more citing papers are in PubMed but not listed here.

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

11 authors at 5 institutions in 2 countries.

Quanbo JiDepartment of Orthopaedics, General Hospital of Chinese People's Liberation Army, Beijing, China; Department of Orthopaedic Surgery, Stanford University, Stanford, CA, USA.
Xiaojie XuDepartment of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China.
Qi SongDepartment of Oncology, General Hospital of Chinese People's Liberation Army, Beijing, China.
Yameng XuDepartment of Traditional Chinese Medicine, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yanhong TaiDepartment of Pathology, the 307 Hospital of Chinese People's Liberation Army, Beijing, China.
Stuart B GoodmanDepartment of Orthopaedic Surgery, Stanford University, Stanford, CA, USA.
Wenzhi BiDepartment of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China.
Meng XuDepartment of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, China.
Shunchang JiaoDepartment of Oncology, General Hospital of Chinese People's Liberation Army, Beijing, China.
William J MaloneyDepartment of Orthopaedic Surgery, Stanford University, Stanford, CA, USA. Electronic address: wmaloney@stanford.edu.
Yan WangDepartment of Orthopaedics, General Hospital of Chinese People's Liberation Army, Beijing, China. Electronic address: yanwang301@126.com.
Beijing VDJBio (China) · CNChinese People's Liberation Army · CNStanford University · US307th Hospital of Chinese People’s Liberation Army · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cadherin-6 (CDH6) is aberrantly expressed in cancer and closely associated with tumor progression. However, the functions of CDH6 in human osteosarcoma and the molecular mechanisms underlying CDH6 in osteosarcoma oncogenesis remain poorly understood. In this work, we assessed the role of CDH6 in human osteosarcoma and identified that the expression of CDH6 was closely related with the overall survival and poor prognosis of osteosarcoma patients. MicroRNAs (miRNAs) have been implicated as important epigenetic regulators during the progression of osteosarcoma. Using dual-luciferase reporter assays, we showed that miR-223-3p suppresses CDH6 expression by directly binding to the 3' UTR of CDH6. miR-223-3p overexpression significantly inhibited cell invasion, migration, growth, and proliferation by suppressing the CDH6 expression in vivo and in vitro. Besides, CDH6 overexpression in the miR-223-3p-transfected osteosarcoma cells effectively rescued the inhibition of cell invasion, migration, growth, and proliferation mediated by miR-223-3p. Additionally, Kaplan-Meier analysis suggests that the expression of miR-223-3p predicts favorable clinical outcomes for osteosarcoma patients. Moreover, the expression of miR-223-3p was downregulated in osteosarcoma patients and was negatively associated with the expression of CDH6. Collectively, these data highlight that miR-223-3p/CDH6 axis is an important novel pleiotropic regulator and could early predict the metastatic potential in human osteosarcoma treatments.

Indexed as

Gene Expression Regulation, NeoplasticRNA Interference3' Untranslated RegionsAnimalsBone NeoplasmsCadherinsCell Line, TumorCell MovementCell ProliferationDisease Models, AnimalDisease ProgressionFemaleHumansImmunohistochemistryKaplan-Meier EstimateMale3' Untranslated RegionsCadherinsK cadherinMicroRNAsMIR223, humanCDH6miR-223-3posteosarcomatherapy

Identifiers

PMID29628305
PMCPMC5993963
OpenAlexW2793740075

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.