Evidence map›Paper›PMID 20851776›Full record

ReviewThe international journal of biochemistry & cell biology2011

Potential applications for cell regulatory factors in liver progenitor cell therapy.

Thomas Shupe, Bryon E Petersen

Abstract readReview
In one paragraph

Review in The international journal of biochemistry & cell biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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

2 authors at 2 institutions in 1 country.

Thomas ShupeDepartment of Pathology, Immunology and Laboratory Medicine, University of Florida, College of Medicine, Gainesville, FL 32610-0275, USA. petersen@pathology.ufl.edu
Bryon E Petersen
University of Florida · USUniversity of Florida Health · US

Funding

Mechanisms of Oval Cell Activation and DifferentiationR01DK058614 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PETERSEN, BRYON E · 2001 to 2014
$3.6M
Stem Cells in Liver Regeneration: Fusion or PlasticityR01DK065096 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PETERSEN, BRYON E · 2005 to 2013
$2.7M
Mechanisms of Oval Cell Activation and DifferentiationR56DK058614 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PETERSEN, BRYON E · 2010 to 2010
$451k
NIDDK NIH HHS R01 DK058614NIDDK NIH HHS R01 DK065096NIDDK NIH HHS R56 DK058614
6 · The paper itself

Abstract

Orthotopic liver transplant represent the state of the art treatment for terminal liver pathologies such as cirrhosis in adults and hemochromatosis in neonates. A limited supply of transplantable organs in relationship to the demand means that many patients will succumb to disease before an organ becomes available. One promising alternative to liver transplant is therapy based on the transplant of liver progenitor cells. These cells may be derived from the patient, expanded in vitro, and transplanted back to the diseased liver. Inborn metabolic disorders represent the most attractive target for liver progenitor cell therapy, as many of these disorders may be corrected by repopulation of only a portion of the liver by healthy cells. Another potential application for liver progenitor cell therapy is the seeding of bio-artificial liver matrix. These ex vivo bioreactors may someday be used to bridge critically ill patients to other treatments. Conferring a selective growth advantage to the progenitor cell population remains an obstacle to therapy development. Understanding the molecular signaling mechanisms and micro-environmental cues that govern liver progenitor cell phenotype may someday lead to strategies for providing this selective growth advantage. The discovery of a population of cells within the bone marrow possessing the ability to differentiate into hepatocytes may provide an easily accessible source of cells for liver therapies.

Indexed as

Connective Tissue Growth FactorCytokinesInsulin-Like Growth Factor Binding Protein 3SomatostatinStem Cell TransplantationAnimalsHepatocytesHumansLiverLiver DiseasesLiver RegenerationTissue ScaffoldsConnective Tissue Growth FactorCytokinesInsulin-Like Growth Factor Binding Protein 3Somatostatin

Identifiers

PMID20851776
PMCPMC3022095
OpenAlexW2039609191

What OpenQuestion holds

Textmetadata
LicenceTDM
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.