Evidence map›Paper›PMID 35360393›Full record

ReviewFrontiers in bioengineering and biotechnology2022

Re-Endothelialization of Decellularized Liver Scaffolds: A Step for Bioengineered Liver Transplantation.

Kewei Li, Mohammad Tharwat, Ellen L Larson, Philipp Felgendreff, Seyed M Hosseiniasl, Anan Abu Rmilah, Khaled Safwat, Jeffrey J Ross, Scott L Nyberg

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in bioengineering and biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. 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 at 6 institutions in 4 countries.

Kewei LiDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Mohammad TharwatDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Ellen L LarsonDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Philipp FelgendreffDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Seyed M HosseiniaslDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Anan Abu RmilahDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Khaled SafwatGeneral Surgery Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Jeffrey J RossMiromatrix Medical Inc, Eden Prairie, MN, United States.
Scott L NybergDepartment of Surgery, Mayo Clinic, Rochester, MN, United States.
Mayo Clinic in Arizona · USJena University Hospital · DEMayo Clinic · USMiromatrix Medical (United States) · USWest China Hospital of Sichuan University · CNZagazig University · EG

Funding

Immunodeficient FAH-/- PigsR01DK106667 · NIDDK · MAYO CLINIC ROCHESTER · PI NYBERG, SCOTT L · 2015 to 2019
$2.1M
NIDDK NIH HHS R01 DK106667
6 · The paper itself

Abstract

Bioengineered livers (BELs) are an attractive therapeutic alternative to address the donor organ shortage for liver transplantation. The goal of BELs technology aims at replacement or regeneration of the native human liver. A variety of approaches have been proposed for tissue engineering of transplantable livers; the current review will highlight the decellularization-recellularization approach to BELs. For example, vascular patency and appropriate cell distribution and expansion are critical components in the production of successful BELs. Proper solutions to these components of BELs have challenged its development. Several strategies, such as heparin immobilization, heparin-gelatin, REDV peptide, and anti-CD31 aptamer have been developed to extend the vascular patency of revascularized bioengineered livers (rBELs). Other novel methods have been developed to enhance cell seeding of parenchymal cells and to increase graft functionality during both bench and

Indexed as

bioengineered livers (BELs)decellularizationheterotopic transplantationliver transplantationorthotopic transplantationscaffolds

Identifiers

PMID35360393
PMCPMC8960611
OpenAlexW4220855280

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.