Evidence map›Paper›PMID 35184675›Full record

ArticleBioengineered2022

Oncogenic lncRNA ZNFX1 antisense RNA 1 promotes osteosarcoma cells proliferation and metastasis by stabilizing serine and arginine‑rich splicing factor 3.

Yang Zhang, Wenbo Xu, Yanlong Wang, Jianming Li, Guanyi He, Mingyan Guan, Xiangyu Zeng, Wei Bian, Yan Song, Jianyu Liu

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. The regulatory role ofOncology research · 2025
    Pooled it
  2. Review
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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 1 institution in 1 country.

Yang ZhangDepartment of Orthopaedics, The Second Affiliated Hospital of Harbin Medical University, Harbin, P. R. China.
Wenbo XuDepartment of Orthopaedics, The Second Affiliated Hospital of Harbin Medical University, Harbin, P. R. China.
Yanlong WangDepartment of Orthopaedics, The Second Affiliated Hospital of Harbin Medical University, Harbin, P. R. China.
Jianming LiDepartment of Orthopaedics, The Second Affiliated Hospital of Harbin Medical University, Harbin, P. R. China.
Guanyi HeDepartment of Orthopaedics, The Second Affiliated Hospital of Harbin Medical University, Harbin, P. R. China.
Mingyan GuanDepartment of Orthopaedics, The Second Affiliated Hospital of Harbin Medical University, Harbin, P. R. China.
Xiangyu ZengDepartment of Orthopaedics, The Second Affiliated Hospital of Harbin Medical University, Harbin, P. R. China.
Wei BianDepartment of Orthopaedics, The Second Affiliated Hospital of Harbin Medical University, Harbin, P. R. China.
Yan SongDepartment of Operating Room, The Second Affiliated Hospital of Harbin Medical University, Harbin, P. R. China.
Jianyu LiuDepartment of Orthopaedics, The Second Affiliated Hospital of Harbin Medical University, Harbin, P. R. China.ORCID 0000-0002-3046-3167
Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have demonstrated that lncRNAs play an important role in cancers, particularly osteosarcoma. ZFAS1 is a newly identified and characterized lncRNA linked to a variety of cancers. The role of ZFAS1 in osteosarcoma is mainly unknown. This study discovered that ZFAS1 was upregulated in osteosarcoma patient tissues, which correlates with elevated SRSF3 protein levels. Higher levels of ZFAS1 or SRSF3 were linked to a poor prognosis of osteosarcoma. ZFAS1 knockdown decreased SRSF3 protein levels but had a negligible effect on SRSF3 mRNA expression. Further research indicated that ZFAS1 could bind to the SRSF3 protein directly and prevent degrading. Functional studies revealed that ZFAS1 knockdown inhibited osteosarcoma cell proliferation as measured by the CCK-8 assay, colony formation assay, and Ki-67 immunofluorescence staining. Furthermore, ZFAS1 knockdown reduced the expression of PCNA, CDK1, CDK4, and CDK6, increasing p53 and p16. IT has also been observed that ZFAS1 knockdown inhibited osteosarcoma cell migration and invasion as measured by the wound healing assay and the trans-well assay with or without Matrigel.Furthermore, exogenous SRSF3 expression in ZFAS1-depleted osteosarcoma cells restored SRSF3 expression while simultaneously inhibiting cell proliferation and metastasis. Our findings show that ZFAS1 plays an essential role in osteosarcoma progression by stabilizing the SRSF3 protein. Our study provides novel insight into the role of ZFAS1 in osteosarcoma. ZFAS1 has the potential to be used as a prognostic biomarker as well as a therapeutic target in the treatment of osteosarcoma.

Indexed as

Bone NeoplasmsMicroRNAsOsteosarcomaRNA, Long NoncodingSerine-Arginine Splicing FactorsArginineCarcinogenesisCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansArginineMicroRNAsRNA, Long NoncodingSerine-Arginine Splicing FactorsSRSF3 protein, humanZFAS1 long non-coding RNA, humanbiomarkercancer proliferationmetastasisOsteosarcomaSRSF3ZFAS1

Identifiers

PMID35184675
PMCPMC8974064
OpenAlexW4212865769

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.