Evidence map›Paper›PMID 29515136›Full record

ArticleScientific reports2018

Long-term regeneration and remodeling of the pig esophagus after circumferential resection using a retrievable synthetic scaffold carrying autologous cells.

Saverio La Francesca, Johnathon M Aho, Matthew R Barron, Ellen W Blanco, Sherif Soliman, Lena Kalenjian, Ariel D Hanson, Elisaveta Todorova, Matthew Marsh, KaLia Burnette and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
9.9field-weighted citation impact, top 1% 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

29 citing papers in PubMed, 70 citations in OpenAlex.

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  7. Tissue Engineering for Gastrointestinal and Genitourinary Tracts.International journal of molecular sciences · 2022
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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

13 authors at 3 institutions in 1 country.

Saverio La FrancescaBiostage, Inc, Holliston, MA, 01746, USA.
Johnathon M AhoDivision of Thoracic Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, 55905, USA.ORCID 0000-0002-8361-079X
Matthew R BarronDivision of Thoracic Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, 55905, USA.
Ellen W BlancoDivision of Thoracic Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, 55905, USA.
Sherif SolimanBiostage, Inc, Holliston, MA, 01746, USA.
Lena KalenjianBiostage, Inc, Holliston, MA, 01746, USA.
Ariel D HansonBiostage, Inc, Holliston, MA, 01746, USA.
Elisaveta TodorovaBiostage, Inc, Holliston, MA, 01746, USA.
Matthew MarshBiostage, Inc, Holliston, MA, 01746, USA.
KaLia BurnetteBiostage, Inc, Holliston, MA, 01746, USA.
Harout DerSimonianBiostage, Inc, Holliston, MA, 01746, USA.
Robert D OdzeDepartment of Pathology, Harvard Medical School, Boston, MA, 02115, USA.ORCID 0000-0001-7910-8273
Dennis A WigleDivision of Thoracic Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, 55905, USA. aho.johnathon@mayo.edu.
Mayo Clinic in Arizona · USHarvard University · USMayo Clinic · US

Funding

Training Program in Cell, Molecular, and Developmental BiologyT32GM008111 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YODER, BRADLEY K. · 1985 to 2022
$5.4M
Interdisciplinary Training in Lung Physiology and Biomedical EngineeringT32HL105355 · NHLBI · MAYO CLINIC ROCHESTER · PI PRAKASH, Y. S., SIECK, GARY C. · 2012 to 2021
$3.9M
NHLBI NIH HHS T32 HL105355NIGMS NIH HHS T32 GM008111
6 · The paper itself

Abstract

Treatment of esophageal disease can necessitate resection and reconstruction of the esophagus. Current reconstruction approaches are limited to utilization of an autologous conduit such as stomach, small bowel, or colon. A tissue engineered construct providing an alternative for esophageal replacement in circumferential, full thickness resection would have significant clinical applications. In the current study, we demonstrate that regeneration of esophageal tissue is feasible and reproducible in a large animal model using synthetic polyurethane electro-spun grafts seeded with autologous adipose-derived mesenchymal stem cells (aMSCs) and a disposable bioreactor. The scaffolds were not incorporated into the regrown esophageal tissue and were retrieved endoscopically. Animals underwent adipose tissue biopsy to harvest and expand autologous aMSCs for seeding on electro-spun polyurethane conduits in a bioreactor. Anesthetized pigs underwent full thickness circumferential resection of the mid-lower thoracic esophagus followed by implantation of the cell seeded scaffold. Results from these animals showed gradual structural regrowth of endogenous esophageal tissue, including squamous esophageal mucosa, submucosa, and smooth muscle layers with blood vessel formation. Scaffolds carrying autologous adipose-derived mesenchymal stem cells may provide an alternative to the use of a gastro-intestinal conduit for some patients following resection of the esophagus.

Indexed as

Cells, ImmobilizedEsophageal DiseasesEsophagusRegenerationAnimalsAutograftsDisease Models, AnimalMesenchymal Stem CellsMesenchymal Stem Cell TransplantationSwineTissue EngineeringTissue Scaffolds

Identifiers

PMID29515136
PMCPMC5841275
OpenAlexW2794433880

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.