Evidence map›Paper›PMID 34873899›Full record

ArticleEuropean journal of histochemistry : EJH2021

miR-1270 enhances the proliferation, migration, and invasion of osteosarcoma <em>via</em> targeting cingulin.

Yang Liu, Weichun Guo, Shuo Fang, Bin He, Xiaohai Li, Li Fan

Open access · goldAbstract read
In one paragraph

Article in European journal of histochemistry : EJH, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. The Role of Centrosome Misorientation and miR-1270 in Impaired Endothelial Cell Migration in Preeclampsia.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  2. Review
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  4. Article
  5. Topology and Dynamics of Transcriptome (Dys)Regulation.International journal of molecular sciences · 2024
    Article
  6. Article
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  9. 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

6 authors at 1 institution in 1 country.

Yang LiuDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan. liuyangwhu@sina.com.
Weichun GuoDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan. weichunguo@tom.com.
Shuo FangDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan. 601028347@qq.com.
Bin HeDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan. hebin@whu.edu.cn.
Xiaohai LiDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan. 591247950@qq.com.
Li FanDepartment of Orthopedics, Renmin Hospital of Wuhan University, Wuhan. 13006183037@163.com.
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS), characterized by high morbidity and mortality, is the most common bone malignancy worldwide. MicroRNAs (miRNAs) play a crucial role in the initiation and development of OS. The purpose of this study was to investigate the roles of miR-1270 in OS. RT-qPCR and Western blot were applied to detect the mRNA and protein level, respectively. CCK-8, colony formation, and TUNEL assays were conducted to determine the cell viability, proliferation, and apoptosis of OS cells. Wound healing and transwell assay were performed to detect the migration and invasion ability of OS cells. Bioinformatics analysis and dual-luciferase reporter assay were used to predict the target genes of miR-1270. Tumor xenograft in vivo assay was carried out to determine miR-1270 effect on the tumor size, volume, and weight. In this study, miR-1270 was overexpressed in OS tissues and cells. However, miR-1270 knockdown inhibited the proliferation, migration and invasion, and promoted the OS cells' apoptosis. Mechanistically, cingulin (CGN) was predicted and proved to be a target of miR-1270 and partially alleviated the effects of miR-1270 on the proliferation, migration and invasion ability of OS cells. Taken together, knockdown of miR-1270 may inhibit the development of OS via targeting CGN. This finding may provide a novel therapeutic strategy for OS.

Indexed as

Cell MovementCell ProliferationBone NeoplasmsCell Line, TumorHumansMembrane ProteinsMicrofilament ProteinsMicroRNAsNeoplasm InvasivenessNeoplasm ProteinsOsteosarcomaRNA, NeoplasmCGN protein, humanMembrane ProteinsMicrofilament ProteinsMicroRNAsMIRN1270 microRNA, humanNeoplasm ProteinsRNA, Neoplasm

Identifiers

PMID34873899
PMCPMC8678625
OpenAlexW4200552285

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.