Evidence map›Paper›PMID 29330462›Full record

ArticleScientific reports2018

miR-143-3p inhibits the proliferation, migration and invasion in osteosarcoma by targeting FOSL2.

Xiangran Sun, Guo Dai, Ling Yu, Qingzhu Hu, Jingteng Chen, Weichun Guo

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
7.7field-weighted citation impact, top 1% 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

76 citing papers in PubMed, 137 citations in OpenAlex.

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  7. Progress in the Study of Fra-2 in Respiratory Diseases.International journal of molecular sciences · 2024
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  10. Role of Fra-2 in cancer.Cell death and differentiation · 2024
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16 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

6 authors at 2 institutions in 1 country.

Xiangran SunDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei Province, P. R. China.
Guo DaiDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei Province, P. R. China.
Ling YuDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei Province, P. R. China.
Qingzhu HuDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei Province, P. R. China.
Jingteng ChenDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei Province, P. R. China.
Weichun GuoDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei Province, P. R. China. guoweichun@aliyun.com.
Wuhan University · CNRenmin Hospital of Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS) is the most common type of primary malignant bone tumor and mainly occurs in children and adolescent. Because of its early migration and invasion, OS has a poor prognosis. It has been reported that mircoRNAs (miRNAs) play a crucial role in the occurrence and development of multiple tumors. In this study, we identified the aberrant-expression of miR-143-3p in osteosarcoma and examined the role of miR-143-3p in OS development. Further, we searched the miR-143-3p target gene and verified its accuracy by luciferase experiments. Finally, we explored the relationship between miR-143-3p and FOS-Like antigen 2 (FOSL2). Our data indicated that miR-143-3p expression was substantially lower in OS tissues and cell-line compared with normal tissues, and was lower in patients with poor prognosis. In addition miR-143-3p inhibited OS cell proliferation and metastasis while promoting apoptosis. We next showed that FOSL2 was directly targeted by miR-143-3p and could reverse the inhibition caused by miR-143-3p. Finally, we found FOSL2 expression in OS cells was significantly higher compared with normal cells and negatively correlated with miR-143-3p. Thus, miR-143-3p directly and negatively targets FOSL2 to affect OS characteristics. This provides a new target for the treatment of OS and deserves further study.

Indexed as

3' Untranslated RegionsBone NeoplasmsCell Line, TumorCell ProliferationDown-RegulationFemaleFos-Related Antigen-2Gene Expression Regulation, NeoplasticHumansMaleMicroRNAsNeoplasm InvasivenessOsteosarcoma3' Untranslated RegionsFOSL2 protein, humanFos-Related Antigen-2MicroRNAsMIRN143 microRNA, human

Identifiers

PMID29330462
PMCPMC5766605
OpenAlexW2783670975

What Socratic holds

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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.