Evidence map›Paper›PMID 32323794›Full record

ArticleOncology reports2020

miR‑95 promotes osteosarcoma growth by targeting SCNN1A.

Yannan Geng, Shaorong Zhao, Yutao Jia, Gang Xia, Huiming Li, Zhao Fang, Quan Zhang, Rong Tian

Abstract read
In one paragraph

Article in Oncology reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Eight Differential miRNAs in DN Identified by Microarray Analysis as Novel Biomarkers.Diabetes, metabolic syndrome and obesity : targets and therapy · 2022
    Article
  9. International journal of general medicine · 2022
    Article
  10. Article
  11. Review
  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

8 authors.

Yannan Geng *Department of Spinal Surgery, Tianjin Union Medical Center, Tianjin 300121, P.R. China.
Shaorong Zhao *The 3rd Department of Breast Cancer, China Tianjin Breast Cancer Prevention, Treatment and Research Center, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center of Cancer, Tianjin 300060, P.R. China.
Yutao JiaDepartment of Spinal Surgery, Tianjin Union Medical Center, Tianjin 300121, P.R. China.
Gang XiaDepartment of Spinal Surgery, Tianjin Union Medical Center, Tianjin 300121, P.R. China.
Huiming LiDepartment of Spinal Surgery, Tianjin Union Medical Center, Tianjin 300121, P.R. China.
Zhao FangDepartment of Spinal Surgery, Tianjin Union Medical Center, Tianjin 300121, P.R. China.
Quan ZhangDepartment of Spinal Surgery, Tianjin Union Medical Center, Tianjin 300121, P.R. China.
Rong TianDepartment of Spinal Surgery, Tianjin Union Medical Center, Tianjin 300121, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS) is a common malignant bone tumor, presenting particularly in children and young adults, and accounts for approximately 19% of all malignant bone cancers. Despite advances in OS treatment, long‑term prognosis remains poor. miRNAs are non‑coding single‑stranded RNAs ~22 nucleotides in length. Increasing evidence suggests that numerous miRNAs may play critical roles in tumorigenesis and tumor progression; however, the role of miR‑95 in OS has not been examined. In the present study, we investigated the role of miR‑95 in OS using in vitro and in vivo models and publicly available expression data. Our findings indicate that abnormal miR‑95 expression occurs in OS, according to the Gene Expression Omnibus (GEO) database. The miR‑95 inhibitor reduced cell proliferation and promoted apoptosis in OS cell lines as detected by EdU staining, TUNEL staining and flow cytometry. Furthermore, a dual luciferase reporter assay revealed that miR‑95 regulates the cell cycle of OS cells and apoptosis by targeting sodium channel epithelial 1α subunit (SCNN1A). Additionally, miR‑95 antagomir suppressed the growth of U2OS xenograft tumors in a mouse model. In summary, our results suggest that miR‑95 induces OS growth in vitro and in vivo by targeting SCNN1A. Our results help clarify the mechanism underlying the miR‑95‑mediated effects on OS tumor growth, thus potentially establishing it as a diagnostic target.

Indexed as

Up-RegulationAnimalsApoptosisBone NeoplasmsCase-Control StudiesCell Line, TumorCell MovementCell ProliferationEpithelial Sodium ChannelsGene Expression Regulation, NeoplasticHumansMaleMiceMicroRNAsNeoplasm TransplantationOsteosarcomaEpithelial Sodium ChannelsMicroRNAsMIRN95 microRNA, humanSCNN1A protein, humancell apoptosiscell cyclemiR-95osteosarcomaSCNN1A

Identifiers

PMID32323794
PMCPMC7107771

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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.