Evidence map›Paper›PMID 33816232›Full record

ArticleFrontiers in oncology2021

Silencing of HuR Inhibits Osteosarcoma Cell Epithelial-Mesenchymal Transition

Yongming Liu, Yuan Zhang, Jinxue Zhang, Jingchang Ma, Xuexue Xu, Yuling Wang, Ziqing Zhou, Dongxu Jiang, Shen Shen, Yong Ding and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. 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
1.0field-weighted citation impact, top 30% 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, 16 citations in OpenAlex.

  1. Review
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  9. RNA-binding proteins in bone pathophysiology.Frontiers in cell and developmental biology · 2024
    Review
  10. LncRNAs in oncogenic microenvironment: from threat to therapy.Frontiers in cell and developmental biology · 2024
    Review
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  12. Article
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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

12 authors at 2 institutions in 1 country.

Yongming LiuOrthopedic Department of Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Yuan ZhangInstitute of Medical Research, Northwestern Polytechnical University, Xi'an, China.
Jinxue ZhangOrthopedic Department of Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Jingchang MaDepartment of Immunology, The Fourth Military Medical University, Xi'an, China.
Xuexue XuInstitute of Medical Research, Northwestern Polytechnical University, Xi'an, China.
Yuling WangDepartment of Immunology, The Fourth Military Medical University, Xi'an, China.
Ziqing ZhouDepartment of Immunology, The Fourth Military Medical University, Xi'an, China.
Dongxu JiangDepartment of Immunology, The Fourth Military Medical University, Xi'an, China.
Shen ShenDepartment of Immunology, The Fourth Military Medical University, Xi'an, China.
Yong DingOrthopedic Department of Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Yong ZhouOrthopedic Department of Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Ran ZhuangInstitute of Medical Research, Northwestern Polytechnical University, Xi'an, China.
Air Force Medical University · CNNorthwestern Polytechnical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteosarcoma (OS) is a highly malignant and aggressive bone tumor. This study was performed to explore the mechanisms of HuR (human antigen R) in the progression of OS.

methodsHuR expression levels in OS tissues and cells were detected by immunohistochemistry and western blotting. HuR siRNA was transfected into SJSA-1 OS cells to downregulate HuR expression, and then cell proliferation, migration, and epithelial-mesenchymal transition (EMT) were evaluated. RNA immunoprecipitation was performed to determine the association of the long non-coding RNA (lncRNA) XIST and argonaute RISC catalytic component (AGO) 2 with HuR. Fluorescence

resultsKnockdown of HuR repressed OS cell migration and EMT. AGO2 was identified as a target of HuR and silencing of HuR decreased AGO2 expression. The lncRNA XIST was associated with HuR-mediated AGO2 suppression. Moreover, knockdown of AGO2 significantly inhibited cell proliferation, migration, and EMT in OS.

conclusionOur findings indicate that HuR knockdown suppresses OS cell EMT by regulating lncRNA XIST/AGO2 signaling.

Indexed as

AGO2epithelial-mesenchymal transitionHuRlong non-coding RNA XISTmigrationosteosarcoma

Identifiers

PMID33816232
PMCPMC8017292
OpenAlexW3139467425

What OpenQuestion holds

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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.