Evidence map›Paper›PMID 30654068›Full record

ArticleJournal of hepatology2019

Radiation-primed hepatocyte transplantation in murine monogeneic dyslipidemia normalizes cholesterol and prevents atherosclerosis.

Mark Barahman, Wei Zhang, Hillary Yaffe Harris, Anita Aiyer, Rafi Kabarriti, Milan Kinkhabwala, Namita Roy-Chowdhury, Amanda P Beck, Thomas S Scanlan, Jayanta Roy-Chowdhury and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of hepatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. [Progress in basic research and clinical application of hepatocyte transplantation].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Mark BarahmanDepartment of Pathology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States.
Wei ZhangDepartment of Pathology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States.
Hillary Yaffe HarrisDepartment of Surgery, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States.
Anita AiyerDepartment of Radiation Oncology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States.
Rafi KabarritiDepartment of Radiation Oncology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States.
Milan KinkhabwalaDepartment of Surgery, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States.
Namita Roy-ChowdhuryDepartment of Medicine, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States; Department of Genetics, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States; The Marion Bessin Liver Research Center, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States.
Amanda P BeckDepartment of Pathology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States.
Thomas S ScanlanDepartments of Physiology and Pharmacology, Oregon Health & Science University, Portland, OR, United States.
Jayanta Roy-ChowdhuryDepartment of Medicine, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States; Department of Genetics, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States; The Marion Bessin Liver Research Center, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States.
Patrik AspDepartment of Surgery, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States.
Chandan GuhaDepartment of Pathology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States; Department of Surgery, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States; Department of Radiation Oncology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States; Department of Medicine, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States; The Marion Bessin Liver Research Center, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States; Department of Urology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY, United States. Electronic address: cguhamd@gmail.com.
Albert Einstein College of Medicine · USMontefiore Medical Center · USOregon Health & Science University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007288 · NIGMS · YESHIVA UNIVERSITY · PI AKABAS, MYLES H. · 1985 to 2022
$35.6M
Stable Isotope and Metabolomics CoreP60DK020541 · NIDDK · YESHIVA UNIVERSITY · PI FLEISCHER, NORMAN S. · 1986 to 2014
$29.8M
Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
Special Animal CoreP30DK041296 · NIDDK · YESHIVA UNIVERSITY · PI WOLKOFF, ALLAN W · 1989 to 2018
$22.9M
Core-010UL1TR001073 · NCATS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI KELLER, MARLA J, SHAMOON, HARRY · 2013 to 2017
$21.3M
Thyroid Hormone ActionR01DK052798 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SCANLAN, THOMAS STERLING · 1997 to 2020
$5.7M
Stromal cell therapy as a treatment against Gastrointestinal Acute Radiation Syndrome (GI-ARS)U01AI138324 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI GUHA, CHANDAN · 2018 to 2022
$2.9M
Development of thrombopoietin mimetic (TPOm) as a mitigator against Radiation-induced endovascular injuriesU01AI133608 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI GHOSH, SANCHITA P, GUHA, CHANDAN · 2017 to 2021
$2.4M
Deriving hepatocytes from disease specific iPS to treat metabolic liver disordersR01DK092469 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI ROY-CHOWDHURY, NAMITA · 2013 to 2016
$1.8M
NCATS NIH HHS UL1 TR001073NIAID NIH HHS U01 AI133608NIAID NIH HHS U01 AI138324NIDDK NIH HHS P30 DK020541NIDDK NIH HHS P30 DK041296NIDDK NIH HHS P60 DK020541NIDDK NIH HHS R01 DK052798NIDDK NIH HHS R01 DK092469NIGMS NIH HHS T32 GM007288
6 · The paper itself

Abstract

BACKGROUND &

aimsInherited abnormalities in apolipoprotein E (ApoE) or low-density lipoprotein receptor (LDLR) function result in early onset cardiovascular disease and death. Currently, the only curative therapy available is liver transplantation. Hepatocyte transplantation is a potential alternative; however, physiological levels of hepatocyte engraftment and repopulation require transplanted cells to have a competitive proliferative advantage of over host hepatocytes. Herein, we aimed to test the efficacy and safety of a novel preparative regimen for hepatocyte transplantation.

methodsHerein, we used an ApoE-deficient mouse model to test the efficacy of a new regimen for hepatocyte transplantation. We used image-guided external-beam hepatic irradiation targeting the median and right lobes of the liver to enhance cell transplant engraftment. This was combined with administration of the hepatic mitogen GC-1, a thyroid hormone receptor-β agonist mimetic, which was used to promote repopulation.

resultsThe non-invasive preparative regimen of hepatic irradiation and GC-1 was well-tolerated in ApoE

conclusionsSignificant hepatic repopulation and the cure of dyslipidemia in this model, using a novel and well-tolerated preparative regimen, demonstrate the clinical potential of applying this method to the treatment of inherited metabolic diseases of the liver. LAY SUMMARY: Hepatocyte transplantation is a promising alternative to liver transplantation for the treatment of liver diseases. However, it is inefficient, as restricted growth of transplanted cells in the liver limits its therapeutic benefits. Preparative treatments improve the efficiency of this procedure, but no clinically-feasible options are currently available. In this study we develop a novel well-tolerated preparative treatment to improve growth of cells in the liver and then demonstrate that this treatment completely cures an inherited lipid disorder in a mouse model.

Indexed as

AcetatesAnimalsApolipoproteins EAtherosclerosisCholesterolDisease Models, AnimalDyslipidemiasFemaleHepatocytesHyperlipoproteinemia Type IIMaleMiceMice, Inbred C57BLPhenolsAcetatesApolipoproteins ECholesterolGC 1 compoundPhenolsApoECell transplantationDyslipidemiaFamilial hypercholesterolemiaHepatocyte transplantationLiver-based metabolic diseasePreparative hepatic irradiation

Identifiers

PMID30654068
PMCPMC6986679
OpenAlexW2910095519

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.