Evidence map›Paper›PMID 32587236›Full record

ArticleCell death & disease2020

LncRNA ENST00000563492 promoting the osteogenesis-angiogenesis coupling process in bone mesenchymal stem cells (BMSCs) by functions as a ceRNA for miR-205-5p.

Zhengxiao Ouyang, Tingting Tan, Xianghong Zhang, Jia Wan, Yanling Zhou, Guangyao Jiang, Daishui Yang, Tang Liu

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. miR‑205: A dual regulator of angiogenesis in health and disease (Review).International journal of molecular medicine · 2026
    Review
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  5. Article
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  10. Review
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  13. Article
  14. Review
  15. Long noncoding RNAPeerJ · 2022
    Article
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  17. Article
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  20. Review
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 at 2 institutions in 1 country.

Zhengxiao OuyangDepartment of Orthopedics, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, P. R. China.
Tingting TanDepartment of Immunology, Xiangya School of Medicine, Central South University, 88 Xiangya Rd, 410008, Changsha, Hunan, P. R. China.
Xianghong ZhangDepartment of Orthopedics, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, P. R. China.
Jia WanDepartment of Orthopedics, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, P. R. China.
Yanling ZhouDepartment of Orthopedics, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, P. R. China.
Guangyao JiangDepartment of Orthopedics, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, P. R. China.
Daishui YangDepartment of Orthopedics, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, P. R. China.
Tang LiuDepartment of Orthopedics, The Second Xiangya Hospital, Central South University, 410011, Changsha, Hunan, P. R. China. liutang1204@csu.edu.cn.
Central South University · CNSecond Xiangya Hospital of Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pain, physical dysfunction, and mental disorders caused by bone nonunion bring great burden to patients. Bone mesenchymal stem cells (BMSCs) isolated from bone nonunion patients with poor proliferation and osteogenic ability are compared with that from normal bone-healing patients. Long noncoding RNAs (lncRNAs) are a class of RNAs that are more than 200 nucleotides in length, lack an open-reading frame encoding a protein, and have little or no protein-coding function, and could regulate gene expression, which is involved in the regulation of important life activities, such as growth, development, aging, and death at epigenetic, transcriptional, and post-transcriptional levels. In this study, we intended to investigate the difference of lncRNA expression between patients with nonunion and normal fracture healing. Our result found that lncRNA ENST00000563492 was downregulated in bone nonunion tissues. LncRNA ENST00000563492 promotes osteogenic differentiation of BMSCs through upregulating the expression of CDH11. On the other hand, LncRNA ENST0000563492 could improve the osteogenesis-angiogenesis coupling process through enhancing the expression of VEGF during osteogenic differentiation of BMSCs. LncRNA ENST00000563492 functions as a ceRNA for miR-205-5p that was targeting CDH11 and VEGF. LncRNA ENST00000563492 could promote the osteogenesis of BMSCs in vivo. Our result indicated that lncRNA ENST00000563492 may be a new target for bone nonunion.

Indexed as

Adultbeta CateninBone and BonesBone RegenerationCadherinsDown-RegulationFemaleFracture HealingFractures, UnunitedHumansHuman Umbilical Vein Endothelial CellsMaleMesenchymal Stem CellsMicroRNAsMiddle AgedNeovascularization, Physiologicbeta CateninCadherinsMicroRNAsMIR205, humanosteoblast cadherinRNA, Long NoncodingVascular Endothelial Growth Factor A

Identifiers

PMID32587236
PMCPMC7316863
OpenAlexW3037631102

What OpenQuestion 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 OpenQuestion graph.