Evidence map›Paper›PMID 36382023›Full record

ArticleBioactive materials2023

Harnessing the synergy of perfusable muscle flap matrix and adipose-derived stem cells for prevascularization and macrophage polarization to reconstruct volumetric muscle loss.

Qixu Zhang, Yulun Chiu, Youbai Chen, Yewen Wu, Lina W Dunne, Rene D Largo, Edward I Chang, David M Adelman, Mark V Schaverien, Charles E Butler

Open access · goldAbstract read
In one paragraph

Article in Bioactive materials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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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

10 authors at 1 institution in 2 countries.

Qixu ZhangDepartment of Plastic Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Yulun ChiuDepartment of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Youbai ChenDepartment of Plastic Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Yewen WuDepartment of Plastic Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Lina W DunneDepartment of Plastic Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Rene D LargoDepartment of Plastic Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Edward I ChangDepartment of Plastic Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
David M AdelmanDepartment of Plastic Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Mark V SchaverienDepartment of Plastic Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Charles E ButlerDepartment of Plastic Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Muscle flaps must have a strong vascular network to support a large tissue volume and ensure successful engraftment. We developed porcine stomach musculofascial flap matrix (PDSF) comprising extracellular matrix (ECM) and intact vasculature. PDSF had a dominant vascular pedicle, microcirculatory vessels, a nerve network, well-retained 3-dimensional (3D) nanofibrous ECM structures, and no allo- or xenoantigenicity. In-depth proteomic analysis demonstrated that PDSF was composed of core matrisome proteins (e.g., collagens, glycoproteins, proteoglycans, and ECM regulators) that, as shown by Gene Ontology term enrichment analysis, are functionally related to musculofascial biological processes. Moreover, PDSF-human adipose-derived stem cell (hASC) synergy not only induced monocytes towards IL-10-producing M2 macrophage polarization through the enhancement of hASCs' paracrine effect but also promoted the proliferation and interconnection of both human skeletal muscle myoblasts (HSMMs) and human umbilical vein endothelial cells (HUVECs) in static triculture conditions. Furthermore, PDSF was successfully prevascularized through a dynamic perfusion coculture of hASCs and HUVECs, which integrated with PDSF and induced the maturation of vascular networks

Indexed as

DecellularizationExtracellular matrixMacrophage polarizationMuscle flap fabricationVascularizationVolumetric muscle loss

Identifiers

PMID36382023
PMCPMC9646752
OpenAlexW4308100849

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.