Evidence map›Paper›PMID 27304058›Full record

ArticleOncotarget2016

miR-145 promotes osteosarcoma growth by reducing expression of the transcription factor friend leukemia virus integration 1.

Panfeng Wu, Jieyu Liang, Fang Yu, Zhengbing Zhou, Juyu Tang, Kanghua Li

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  6. Review
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  8. Review
  9. miRNA signatures in childhood sarcomas and their clinical implications.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2019
    Review
  10. Article
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  12. Review
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  15. Mir-150 Up-Regulates Glut1 and Increases Glycolysis in Osteosarcoma CellsAsian Pacific journal of cancer prevention : APJCP · 2017
    Article
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.

Panfeng WuDepartment of Orthopedics, Xiang Ya Hospital Central South University, Changsha, Hunan, People's Republic of China.
Jieyu LiangDepartment of Orthopedics, Xiang Ya Hospital Central South University, Changsha, Hunan, People's Republic of China.
Fang YuDepartment of Orthopedics, Xiang Ya Hospital Central South University, Changsha, Hunan, People's Republic of China.
Zhengbing ZhouDepartment of Orthopedics, Xiang Ya Hospital Central South University, Changsha, Hunan, People's Republic of China.
Juyu TangDepartment of Orthopedics, Xiang Ya Hospital Central South University, Changsha, Hunan, People's Republic of China.
Kanghua LiDepartment of Orthopedics, Xiang Ya Hospital Central South University, Changsha, Hunan, People's Republic of China.
Xiangya Hospital Central South University · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS) is the most common malignant bone tumor in children and young adults. miR-145 is a microRNA highly expressed in vascularized tissues and has been widely studied in cancers. In this study, we explored the expression and function of miR-145 in OS. We found that miR-145 was consistently under-expressed in OS tissues and cell lines as compared to normal bone tissues and osteoblast cells. Ectopic expression of miR-145 in OS cells inhibited their proliferation and migration and induced apoptosis. miR-145 targets a putative microRNA regulatory element (MRE) in the 3'-UTR of friend leukemia virus integration 1 gene (FLI-1), and its abundance was inversely related to FLI-1 expression in OS tissues and cell lines. miR-145 decreased expression FLI-1 protein and mRNA, but mutation of the miR-145 MRE sequence in the FLI-1 3'-UTR abolished the activity of miR-145 in a reporter assay. Restored expression of FLI-1 diminished miR-145-mediated suppression of tumor progression. These results suggest that miR-145 acts as a tumor suppressor by directly reducing expression of FLI-1, and that the miR-145/FLI-1 pathway is important for tumor progression in OS.

Indexed as

3' Untranslated RegionsAnimalsApoptosisBone NeoplasmsCell Line, TumorCell MovementCell ProliferationDisease ProgressionGene Expression ProfilingGene Expression Regulation, NeoplasticGenes, ReporterHumansMiceMice, NudeMicroRNAsNeoplasm Transplantation3' Untranslated RegionsFLI1 protein, humanMicroRNAsMIRN145 microRNA, humanProto-Oncogene Protein c-fli-1FLI-1miR-145osteosarcoma

Identifiers

PMID27304058
PMCPMC5173131
OpenAlexW2416133564

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.