Evidence map›Paper›PMID 41126688›Full record

ArticleAdvanced healthcare materials2026

Geometrically Tunable Scaffold-Free Muscle Bioconstructs for Treating Volumetric Muscle Loss.

Bugra Ayan, Gaoxian Chen, Ishita Jain, Sha Chen, Gladys Chiang, Caroline Hu, Renato Reyes, Beu P Oropeza, Ngan F Huang

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Bugra AyanDepartment of Cardiothoracic Surgery, Stanford University, Stanford, CA, 94305, USA.
Gaoxian ChenDepartment of Cardiothoracic Surgery, Stanford University, Stanford, CA, 94305, USA.
Ishita JainDepartment of Cardiothoracic Surgery, Stanford University, Stanford, CA, 94305, USA.
Sha ChenDepartment of Cardiothoracic Surgery, Stanford University, Stanford, CA, 94305, USA.
Gladys ChiangVeterans Affairs Palo Alto Health Care System, Palo Alto, CA, 94304, USA.
Caroline HuVeterans Affairs Palo Alto Health Care System, Palo Alto, CA, 94304, USA.
Renato ReyesVeterans Affairs Palo Alto Health Care System, Palo Alto, CA, 94304, USA.
Beu P OropezaDepartment of Cardiothoracic Surgery, Stanford University, Stanford, CA, 94305, USA.
Ngan F HuangDepartment of Cardiothoracic Surgery, Stanford University, Stanford, CA, 94305, USA.ORCID 0000-0003-2298-6790

Funding

Development of a Bioengineered Therapeutic Device for the Prevention of LymphedemaR01CA285372 · NCI · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI Ngan F. Huang, Michael Vitoldovich Paukshto · 2024 to 2026
$1.6M
Biomaterials for delivery and maintenance of tip endothelial cellsR21HL172096 · NHLBI · UNIVERSITY OF CALIFORNIA, MERCED · PI HUANG, NGAN F., MCCLOSKEY, KARA E · 2024 to 2025
$643k
Enhance Cell Therapies for Peripheral Arterial Disease Using Human-Compatible Protease-Based ControlsR21HL177570 · NHLBI · STANFORD UNIVERSITY · PI GAO, XIAOJING J, HUANG, NGAN F. · 2025 to 2025
$410k
Novel Highly Regenerative and Scalable Progenitor Cell Exosomes for Treating Peripheral Artery DiseaseR41HL170875 · NHLBI · SERINA THERAPEUTICS, INC. · PI HUANG, NGAN F., LEE, JI EUN · 2023 to 2023
$341k
American Heart Association 24POST1186485BLRD VA I01 BX004259BLRD VA I01 BX006882BLRD VA IK6 BX006309National Science Foundation 1829534National Science Foundation 2227614NCI NIH HHS R01 CA285372NHLBI NIH HHS R21 HL172096NHLBI NIH HHS R21 HL177570NHLBI NIH HHS R41 HL170875NIH HHS R01CA285372NIH HHS R21 HL172096NIH HHS R41HL170875RRD VA I21 RX004898U.S. Department of Veterans Affairs 1I01BX004259U.S. Department of Veterans Affairs IK6BX006309U.S. Department of Veterans Affairs RX004898
6 · The paper itself

Abstract

Traumatic muscle injuries associated with volumetric muscle loss (VML) are characterized by muscle loss beyond intrinsic regeneration capacity, leading to permanent functional impairment. Experimental therapies to augment muscle regeneration, such as cell injection, are limited by low cell transplantation capacity, whereas conventional engineered muscle tissue transplants lack geometric customization to conform to the shape of the muscle defect. Here, a facile approach to engineer scaffold-free high-density muscle tissues in customizable geometric shapes and sizes with high cell viability and integration potential is developed. Using a facile mold-based approach to engineer scaffold-free modular units, transcriptional profiling is performed to uncover the role of pre-formed cell-cell interactions within scaffold-free muscle bioconstructs on myogenesis, an the efficacy of muscle bioconstructs in a mouse model of VML is then evaluated. RNA sequencing revealed that pre-formed cell-cell interactions supported myogenic pathways related to muscle contraction and myofibril assembly, unlike dissociated monodisperse cells. This work further demonstrates the therapeutic efficacy of 3D rectangular solid-shaped scaffold-free transplants in improving muscle function and vascular regeneration. Finally, toward clinical translation, the feasibility of this technology to integrate with medical imaging and artificial intelligence-driven customized bioconstruct design and assembly for intraoperative use is illustrated.

Indexed as

Muscle, SkeletalTissue EngineeringTissue ScaffoldsAnimalsMaleMiceMice, Inbred C57BLMuscle DevelopmentRegenerationgeometrically tunablemodularmuscle regenerationmuscle tissue engineeringscaffold‐freevolumetric muscle loss

Identifiers

PMID41126688
PMCPMC12971103

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.