Evidence map›Paper›PMID 31419653›Full record

ReviewBiomaterials2019

Engineered skeletal muscles for disease modeling and drug discovery.

Jason Wang, Alastair Khodabukus, Lingjun Rao, Keith Vandusen, Nadia Abutaleb, Nenad Bursac

Abstract readReview
In one paragraph

Review in Biomaterials, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
–field-weighted citation impact
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

63 citing papers in PubMed.

  1. Article
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  11. Review
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  14. Review
  15. Muscle Organoid and Assembloid Systems.Advances in experimental medicine and biology · 2025
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

3 more citing papers are in PubMed but not listed here.

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

6 authors.

Jason WangDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Alastair KhodabukusDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Lingjun RaoDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Keith VandusenDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Nadia AbutalebDepartment of Biomedical Engineering, Duke University, Durham, NC, USA.
Nenad BursacDepartment of Biomedical Engineering, Duke University, Durham, NC, USA. Electronic address: nbursac@duke.edu.

Funding

Vascular, Cardiac, and Lung Alveolar Human Microphysiological Systems for SARS-CoV-2 Drug ScreeningUH3TR002142 · NCATS · DUKE UNIVERSITY · PI TRUSKEY, GEORGE A · 2019 to 2021
$4.0M
Interaction of Subchondral Bone and Articular Cartilage System with Skeletal MuscleUH3TR000505 · NCATS · DUKE UNIVERSITY · PI TRUSKEY, GEORGE A · 2014 to 2016
$3.6M
Systemic Inflammation in Microphysiological Models of Muscle and Vascular DiseaseUG3TR002142 · NCATS · DUKE UNIVERSITY · PI TRUSKEY, GEORGE A · 2017 to 2018
$2.1M
Muscle-macrophage constructs for skeletal muscle repairR01AR070543 · NIAMS · DUKE UNIVERSITY · PI BURSAC, NENAD · 2016 to 2020
$1.9M
Translational studies of GAA deficiency in bioengineered human muscleR01AR065873 · NIAMS · DUKE UNIVERSITY · PI BURSAC, NENAD, KOEBERL, DWIGHT D · 2013 to 2017
$1.8M
Engineering a Functional Skeletal MuscleR01AR055226 · NIAMS · DUKE UNIVERSITY · PI BURSAC, NENAD · 2008 to 2012
$1.6M
NCATS NIH HHS UG3 TR002142NCATS NIH HHS UH3 TR000505NCATS NIH HHS UH3 TR002142NIAMS NIH HHS R01 AR055226NIAMS NIH HHS R01 AR065873NIAMS NIH HHS R01 AR070543
6 · The paper itself

Abstract

Skeletal muscle is the largest organ of human body with several important roles in everyday movement and metabolic homeostasis. The limited ability of small animal models of muscle disease to accurately predict drug efficacy and toxicity in humans has prompted the development in vitro models of human skeletal muscle that fatefully recapitulate cell and tissue level functions and drug responses. We first review methods for development of three-dimensional engineered muscle tissues and organ-on-a-chip microphysiological systems and discuss their potential utility in drug discovery research and development of new regenerative therapies. Furthermore, we describe strategies to increase the functional maturation of engineered muscle, and motivate the importance of incorporating multiple tissue types on the same chip to model organ cross-talk and generate more predictive drug development platforms. Finally, we review the ability of available in vitro systems to model diseases such as type II diabetes, Duchenne muscular dystrophy, Pompe disease, and dysferlinopathy.

Indexed as

Drug DiscoveryHumansInduced Pluripotent Stem CellsMuscle, SkeletalMuscular DystrophiesTissue EngineeringHuman muscleInduced pluripotent stem cellsMuscular dystrophy and disease modelingOrgan-on-a-chipRegenerationTissue engineering

Identifiers

PMID31419653
PMCPMC7041662

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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.