Evidence map›Paper›PMID 29075999›Full record

ArticleHuman cell2018

MiR-107 suppresses cell proliferation and tube formation of Ewing sarcoma cells partly by targeting HIF-1β.

Jiajun Chen, Xin Zhou, Qianren Xiao, Tengyu Wang, Gaohai Shao, Yunyun Li, Zhongzu Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2018. 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
2.0field-weighted citation impact, top 12% 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, 21 citations in OpenAlex.

  1. Review
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  5. Article
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  8. Article
  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
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

7 authors at 2 institutions in 1 country.

Jiajun ChenDepartment of Orthopedics, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160, People's Republic of China.
Xin ZhouDepartment of Orthopedics, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160, People's Republic of China.
Qianren XiaoDepartment of Orthopedics, The First Affiliated Hospital, Nanchang University, Nanchang, 330006, Jiangxi, People's Republic of China.
Tengyu WangDepartment of Orthopedics, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160, People's Republic of China.
Gaohai ShaoDepartment of Orthopedics, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160, People's Republic of China.
Yunyun LiDepartment of Gynecology and Obstetrics, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160, People's Republic of China. zzz2lyy@126.com.
Zhongzu ZhangDepartment of Orthopedics, Yongchuan Hospital, Chongqing Medical University, Chongqing, 402160, People's Republic of China. zhangzhongzu@126.com.
Chongqing Medical University · CNNanchang University · CN

Funding

Program of Science and Technology of ChongQing Commission KJ1600228The National Nature Science Foundation of China 81502329
6 · The paper itself

Abstract

MicroRNAs serve a crucial role in the regulation of malignant biological behavior of Ewing's sarcoma (ES). Abnormal expression of miR-107 has been reported in a cohort of cancers, while its exact function in ES remains unclear. Hence, we explored the expression of miR-107 in ES cells and detected its effects on the malignant phenotype of ES cells. Firstly, we perceived the under-expression of miR-107 in human ES cells contrast with the human mesenchymal stem cells. Over-expression of miR-107 restrained cell proliferation and tube formation, arrested cell cycle progression, and facilitated cell apoptosis in SK-ES-1 and RD-ES cell lines. Furthermore, hypoxia inducible factor-1β (HIF-1β) was assumed as a target gene of miR-107. We confirmed the target role of HIF-1β in ES cells. Finally, restoring the expression of HIF-1β could partly abolish miR-107-mediated tumor suppression in ES cells. In conclusion, our results advised that miR-107 suppressed the malignant biological ability of ES cells through targeting HIF-1β.

Indexed as

ApoptosisAryl Hydrocarbon Receptor Nuclear TranslocatorCell Cycle CheckpointsCell Line, TumorCell ProliferationCell Transformation, NeoplasticGene ExpressionHumansMicroRNAsMolecular Targeted TherapySarcoma, EwingARNT protein, humanAryl Hydrocarbon Receptor Nuclear TranslocatorMicroRNAsMIRN107 microRNA, humanEwing’s sarcomaHIF-1βMiR-107Tube formation

Identifiers

PMID29075999
OpenAlexW2767126451

What OpenQuestion holds

Textmetadata
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.