Evidence map›Paper›PMID 10666390›Full record

ArticleThe American journal of pathology2000

Liver regeneration in rats with retrorsine-induced hepatocellular injury proceeds through a novel cellular response.

G J Gordon, W B Coleman, D C Hixson, J W Grisham

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 191 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Distinct hepatocyte identities in liver homeostasis and regeneration.JHEP reports : innovation in hepatology · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Cell competition in liver carcinogenesis.World journal of hepatology · 2020
    Review
  12. Article
  13. Article
  14. Article
  15. Role of liver stem cells in hepatocarcinogenesis.World journal of stem cells · 2014
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

G J GordonDepartment of Pathology, Curriculum in Toxicology, UNC Lineberger Comprehensive Cancer Center, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
W B Coleman
D C Hixson
J W Grisham
UNC Lineberger Comprehensive Cancer CenterRhode Island Hospital · USUniversity of North Carolina at Chapel Hill · US

Funding

ISOLATION OF A HUMAN 11P112 LIVER TUMOR SUPPRESSOR GENER01CA078434 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI COLEMAN, WILLIAM B · 1998 to 2007
$1.8M
CLONAL ANALYSIS OF CARCINOGENESIS IN VITROR01CA029323 · NCI · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI GRISHAM, JOE W · 1985 to 2002
$944k
CLONAL ANALYSIS OF CARCINOGENESIS IN VITROR37CA029323 · NCI · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI GRISHAM, JOE W · 1990 to 1997
–
NCI NIH HHS CA29323NCI NIH HHS CA78434NCI NIH HHS R01 CA078434
6 · The paper itself

Abstract

The adult rodent liver contains at least two recognized populations of cells with stem-like properties that contribute to liver repair/regeneration under different pathophysiological circumstances: (i) unipotential committed progenitor cells (differentiated hepatocytes and biliary epithelial cells) and (ii) multipotential nonparenchymal progenitor cells (oval cells). In retrorsine-induced hepatocellular injury the capacity of fully differentiated rat hepatocytes to replicate is severely impaired and massive proliferation of oval cells does not occur. Nevertheless, retrorsine-exposed rats can replace their entire liver mass after 2/3 surgical partial hepatectomy through the emergence and expansion of a population of small hepatocyte-like progenitor cells that expresses phenotypic characteristics of fetal hepatoblasts, oval cells, and fully differentiated hepatocytes, but differ distinctly from each type of cell. The activation, proliferation, and complete regeneration of normal liver structure from small hepatocyte-like progenitor cells have not been recognized in other models of liver injury characterized by impaired hepatocyte replication. We suggest that the selective emergence and expansion of small hepatocyte-like progenitor cells observed in the retrorsine model reflect a novel mechanism of complete liver regeneration in the adult rat. Furthermore, we suggest that these cells may represent a novel progenitor cell population that (i) responds to liver deficit when the replication capacity of differentiated hepatocytes is impaired, (ii) expresses an extensive proliferative capacity, (iii) can give rise to large numbers of progeny hepatocytes, and (iv) can restore tissue mass.

Indexed as

Liver RegenerationAnimalsCell LineChemical and Drug Induced Liver InjuryHepatectomyLiver DiseasesMalePhenotypePyrrolizidine AlkaloidsRatsRats, Inbred F344Stem CellsPyrrolizidine Alkaloidsretrorsine

Identifiers

PMID10666390
PMCPMC1850042
OpenAlexW1995026118

What OpenQuestion holds

Textmetadata
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.