Evidence map›Paper›PMID 33009207›Full record

ArticleJournal of the Chinese Medical Association : JCMA2021

Nanodiamond-based microRNA delivery system promotes pluripotent stem cells toward myocardiogenic reprogramming.

Chao-Yu Liu, Ming-Cheng Lee, Heng-Fu Lin, Yi-Ying Lin, Wei-Yi Lai, Yueh Chien, Teh-Ia Huo, Wen-Liang Lo, Yuan-Tzu Lan, Yi-Wei Chen and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of the Chinese Medical Association : JCMA, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Synthesis of Multi-Stimuli Responsive FeMolecules (Basel, Switzerland) · 2023
    Article
  5. 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

13 authors at 5 institutions in 1 country.

Chao-Yu LiuDepartment of Surgery, Far-Eastern Memorial Hospital, New Taipei City, Taiwan, ROC.
Ming-Cheng LeeDepartment of Interanl Medicine, Cheng-Hsin General Hospital, Taipei, Taiwan, ROC.
Heng-Fu LinDepartment of Surgery, Far-Eastern Memorial Hospital, New Taipei City, Taiwan, ROC.
Yi-Ying LinInstitute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
Wei-Yi LaiInstitute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
Yueh ChienInstitute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
Teh-Ia HuoInstitute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
Wen-Liang LoInstitute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
Yuan-Tzu LanInstitute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
Yi-Wei ChenInstitute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
Pin-I HuangInstitute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
Yong-Yang LiuInstitute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
Meng-Yin YangDepartment of Neurosurgery, Neurological Institute, Taichung Veterans General Hospital, Taichung, Taiwan, ROC.
Taipei Veterans General Hospital · TWNational Yang Ming Chiao Tung University · TWFar Eastern Memorial Hospital · TWTaichung Veterans General Hospital · TWTaipei Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGene therapy is the advanced therapeutics for supplying or replacing the genetic material in patients with inherited disorders. Recent clinical studies have made some progress in a wide range of applications, including monogenic disorders, neurodegenerative diseases, malignant tumors, and congenital diseases. Heart diseases, especially myocardial ischemia, remain one of the leading causes of mortality worldwide and usually result in irreparable cardiomyocyte damage and severe heart failure.

methodsMost advances in induced pluripotent stem cell (iPSC) technologies for promoting regenerative medicine and stem cell research. However, the driver molecules of myocardial-lineage differentiation and the functional reconstruction capacity of iPSC-derived cardiomyocytes are still an open question. Nanomedicine-based gene delivery provided a crucial platform to carry on the biogenomic materials for equipping functionalities and engineering the living organ environment. Nanodiamond (ND), a carbon-based nanomaterial, has been discovered and shown the high biocompatible and less toxicity for transporting protein, drug, and genomic plasmids.

resultsHere, we applied ND as a gene delivery vehicle to carry microRNA (miR-181a), and then transfected into iPS to promote cardiomyocyte-lineage differentiation. Notably, miR-181a plays a key role in iPS-derived cardiomyocyte differentiation which directly targets Hox-A11, leading to elevated MyoD expression and enhanced cardiomyocyte differentiation.

conclusionOur study demonstrated that miR-181a promotes iPSC differentiation into functional cardiomyocytes. Delivery of NANO-DIAMOND-miR-181a may host clinical potential to enhance the differentiation and recovery of the cardiogenic function in injured cardiomyocytes.

Indexed as

Genetic TherapyNanodiamondsPluripotent Stem CellsHeart DiseasesHumansMicroRNAsMyocytes, CardiacReal-Time Polymerase Chain ReactionMicroRNAsNanodiamonds

Identifiers

PMID33009207
PMCPMC12966113
OpenAlexW3089874960

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.