Evidence map›Paper›PMID 27566578›Full record

ArticleOncotarget2016

Long non-coding RNA HoxA-AS3 interacts with EZH2 to regulate lineage commitment of mesenchymal stem cells.

Xin-Xing Zhu, Ya-Wei Yan, Demeng Chen, Chun-Zhi Ai, Xifeng Lu, Shan-Shan Xu, Shan Jiang, Gen-Shen Zhong, Dong-Bao Chen, Yi-Zhou Jiang

Erratum issuedOpen 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. An erratum has been issued. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

58 citing papers in PubMed, 102 citations in OpenAlex.

  1. Review
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  6. Molecular and Cellular Mechanisms of Osteoporosis.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. The integrated comprehension of lncRNA HOXA-AS3 implication on human diseases.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  14. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 2 countries.

Xin-Xing ZhuInstitute for Advanced Study, Shenzhen University, Shenzhen, Guangdong, China.
Ya-Wei YanInstitute for Advanced Study, Shenzhen University, Shenzhen, Guangdong, China.
Demeng ChenSchool of Dentistry, University of California, Los Angeles, CA, USA.
Chun-Zhi AiInstitute for Advanced Study, Shenzhen University, Shenzhen, Guangdong, China.
Xifeng LuDepartment of Physiology, Center for Diabetes, Obesity and Metabolism, Shenzhen University Health Science Center, Shenzhen University, Shenzhen, Guangdong, China.
Shan-Shan XuInstitute for Advanced Study, Shenzhen University, Shenzhen, Guangdong, China.
Shan JiangInstitute for Advanced Study, Shenzhen University, Shenzhen, Guangdong, China.
Gen-Shen ZhongHenan Key Laboratory of Neural Regeneration and Repairment, The First affiliated Hospital of Xinxiang Medical University, Weihui, Henan, China.
Dong-Bao ChenDepartment of Obstetrics and Gynecology, University of California, Irvine, CA, USA.
Yi-Zhou JiangInstitute for Advanced Study, Shenzhen University, Shenzhen, Guangdong, China.
Shenzhen University · CNFirst Affiliated Hospital of Xinxiang Medical University · CNUniversity of California, Irvine · USUniversity of California, Los Angeles · US

Funding

Epigenetic regulation of endothelial phenotype by flow and hypercholesterolemia in vivo and in vitroK99HL127272 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI JIANG, YIZHOU · 2016 to 2017
$216k
NHLBI NIH HHS K99 HL127272
6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) play an important role in gene regulation and are involving in diverse cellular processes. However, their roles in reprogramming of gene expression profiles during lineage commitment and maturation of mesenchymal stem cells (MSCs) remain poorly understood. In the current study, we characterize the expression of a lncRNA, HoxA-AS3, during the differentiation of MSCs. We showed that HoxA-AS3 is increased upon adipogenic induction of MSCs, while HoxA-AS3 remains unaltered during osteogenic induction. Silencing of HoxA-AS3 in MSCs resulted in decreased adipogenesis and expression of adipogenic markers, PPARG, CEBPA, FABP4 and ADIPOQ. Conversely, knockdown of HoxA-AS3 expression in MSCs exhibited an enhanced osteogenesis and osteogenic markers expression, including RUNX2, SP7, COL1A1, IBSP, BGLAP and SPP1. Mechanistically, HoxA-AS3 interacts with Enhancer Of Zeste 2 (EZH2) and is required for H3 lysine-27 trimethylation (H3K27me3) of key osteogenic transcription factor Runx2. Our data reveal that HoxA-AS3 acts as an epigenetic switch that determines the lineage specification of MSC.

Indexed as

AdipogenesisAnimalsCell DifferentiationCell LineageCell ProliferationCells, CulturedEnhancer of Zeste Homolog 2 ProteinEpigenesis, GeneticGene Expression Regulation, NeoplasticGene SilencingHumansMesenchymal Stem CellsMiceMice, Inbred BALB CMice, Inbred C57BLMice, NudeEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanRNA, Long Noncodingenhancer of zeste homolog 2HoxA-AS3lineage specificationlong non-coding RNAmesenchymal stem cells

Identifiers

PMID27566578
PMCPMC5325385
OpenAlexW2511710681

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.