Evidence map›Paper›PMID 24686813›Full record

ArticlePloS one2014

Knockdown of the HDAC1 promotes the directed differentiation of bone mesenchymal stem cells into cardiomyocytes.

Dong-feng Lu, Ying Wang, Zi-zhuo Su, Zhao-hua Zeng, Xiao-wen Xing, Zhi-yu He, Chunxiang Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
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  9. Silencing nc886, a Non-Coding RNA, Induces Apoptosis of Human Endometrial Cancer Cells-1A In Vitro.Medical science monitor : international medical journal of experimental and clinical research · 2017
    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

7 authors at 3 institutions in 2 countries.

Dong-feng LuDepartment of Cardiology, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Ying WangDepartment of Cardiology, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Zi-zhuo SuDepartment of Cardiology, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Zhao-hua ZengDepartment of Cardiology, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Xiao-wen XingDepartment of Cardiology, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Zhi-yu HeDepartment of Cardiology, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China.
Chunxiang ZhangDepartment of Pharmacology and Cardiovascular Research Center, Rush Medical college of Rush University, Chicago, Illinois, United States of America.
Guangzhou Medical University · CNFirst Affiliated Hospital of Guangzhou Medical University · CNRush University Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Failure of the directed differentiation of the transplanted stem cells into cardiomyocytes is still a major challenge of cardiac regeneration therapy. Our recent study has demonstrated that the expression of histone deacetylase 1 (HDAC1) is decreased in bone mesenchymal stem cells (BMSCs) during their differentiation into cardiomyocytes. However, the potential roles of HDAC1 in cardiac cell differentiation of BMSCs, as well as the mechanisms involved are still unclear. In current study, the expression of HDAC1 in cultured rat BMSCs is knocked down by lentiviral vectors expressing HDAC1-RNAi. The directed differentiation of BMSCs into cardiomyocytes is evaluated by the expression levels of cardiomyocyte-related genes such as GATA-binding protein 4 (GATA-4), Nirenberg, Kim gene 2 homeobox 5 (Nkx2.5), cardiac troponin T (CTnT), myosin heavy chain (MHC), and connexin-43. Compared with that in control BMSCs, the expression of these cardiomyocyte-related genes is significantly increased in these HDAC1 deficient stem cells. The results suggest that HDAC1 is involved in the cardiomyocyte differentiation of BMSCs. Knockdown of the HDAC1 may promote the directed differentiation of BMSCs into cardiomyocytes.

Indexed as

AnimalsBone and BonesCell DifferentiationCells, CulturedGene Knockdown TechniquesHistone Deacetylase 1MaleMesenchymal Stem CellsMyocytes, CardiacRatsRats, Sprague-DawleyStem CellsHdac1 protein, ratHistone Deacetylase 1

Identifiers

PMID24686813
PMCPMC3970960
OpenAlexW2005698941

What OpenQuestion holds

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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.