Evidence map›Paper›PMID 10980117›Full record

ArticleThe American journal of pathology2000

Temporal analysis of hepatocyte differentiation by small hepatocyte-like progenitor cells during liver regeneration in retrorsine-exposed rats.

G J Gordon, W B Coleman, J W Grisham

Abstract 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 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
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

35 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Monitoring Cultured Rat Hepatocytes Using RNA-Seq In Vitro.International journal of molecular sciences · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Role of liver stem cells in hepatocarcinogenesis.World journal of stem cells · 2014
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

3 authors.

G J GordonDepartment of Pathology and Laboratory Medicine, Curriculum in Toxicology, UNC Lineberger Comprehensive Cancer Center, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599, USA.
W B Coleman
J W Grisham

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

Liver regeneration after two-thirds surgical partial hepatectomy (PH) in rats treated with the pyrrolizidine alkaloid retrorsine is accomplished through the activation, expansion, and differentiation of a population of small hepatocyte-like progenitor cells (SHPCs). We have examined expression of the major liver-enriched transcription factors, cytochrome P450 (CYP) enzymes, and other markers of hepatocytic differentiation in SHPCs during the protracted period of liver regeneration after PH in retrorsine-exposed rats. Early-appearing SHPCs (at 3-7 days after PH) express mRNAs for all of the major liver-enriched transcription factors at varying levels compared to fully differentiated hepatocytes. In addition, SHPCs lack (or have significantly reduced) expression of mRNA for hepatocyte markers tyrosine aminotransferase and alpha-1 antitrypsin, but their expression levels of mRNA and/or protein for WT1 and alpha-fetoprotein (AFP) are increased. With the exception of AFP expression, SHPCs resembled fully differentiated hepatocytes by 14 days after PH. Expression of AFP was maintained by most SHPCs through 14 days after PH, gradually declined through 23 days after PH, and was essentially absent from SHPC progeny by 30 days after PH. Furthermore, early appearing SHPCs lack (or have reduced expression) of hepatic CYP proteins known to be induced in rat livers after retrorsine exposure. The resistance of SHPCs to the mitoinhibitory effects of retrorsine may be directly related to a lack of CYP enzymes required to metabolize retrorsine to its toxic derivatives. These results suggest that SHPCs represent a unique parenchymal (less differentiated) progenitor cell population of adult rodent liver that is phenotypically distinct from fully differentiated hepatocytes, biliary epithelial cells, and (ductular) oval cells.

Indexed as

alpha 1-Antitrypsinalpha-FetoproteinsAnimalsAntineoplastic Agents, PhytogenicBiomarkersCell DifferentiationCytochrome P-450 Enzyme SystemDipeptidyl Peptidase 4DNA-Binding ProteinsDNA PrimersHepatectomyImmunoenzyme TechniquesLiverLiver RegenerationMalePyrrolizidine Alkaloidsalpha 1-Antitrypsinalpha-FetoproteinsAntineoplastic Agents, PhytogenicBiomarkersCytochrome P-450 Enzyme SystemDipeptidyl Peptidase 4DNA-Binding ProteinsDNA PrimersPyrrolizidine AlkaloidsretrorsineRNARNA, MessengerTranscription FactorsTyrosine TransaminaseWT1 Proteins

Identifiers

PMID10980117
PMCPMC1885692

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.