Evidence map›Paper›PMID 7485384›Full record

ArticleThe American journal of pathology1995

Expression of matrix proteinases during human intrahepatic bile duct development. A possible role in biliary cell migration.

T Terada, Y Okada, Y Nakanuma

Abstract read
In one paragraph

Article in The American journal of pathology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. A case of small hepatocellular carcinoma with malignant ductular reaction.International journal of clinical and experimental pathology · 2020
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Cutaneous pseudolymphoma: a case report with an immunohistochemical study.International journal of clinical and experimental pathology · 2013
    Article
  12. Malignant intraductal oncocytic papillary neoplasm of the common bile duct.International journal of clinical and experimental pathology · 2012
    Article
  13. Article
  14. Monolobar hepatobiliary fibropolycystic disease.Pathology oncology research : POR · 2011
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Wound healing in the liver with particular reference to stem cells.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 1998
    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

3 authors at 1 institution in 1 country.

T TeradaSecond Department of Pathology, Kanazawa University School of Medicine, Japan.
Y Okada
Y Nakanuma
Kanazawa University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primitive biliary cells are known to migrate from the ductal plate into the mesenchyme during human intrahepatic bile duct development, and this migration process is essential for normal development of intrahepatic bile ducts. However, its molecular mechanism is unknown. Matrix proteinases play an important role in cell migration during cancer invasion and organ development. In this study, we therefore investigated in situ expression of matrix metalloproteinases (MMP) and tissue inhibitors of MMP (TIMP) during human intrahepatic bile duct development, using 32 human fetal livers. We also examined in situ expression of trypsinogen/trypsin, chymotrypsinogen/chymotrypsin, and cathepsin B, which are matrix proteinases and activators of MMP. MMP-1 expression was noted in the ductal plate and migrating primitive biliary cells. MMP-2, MMP-3, and MMP-9 were expressed in the ductal plate. TIMP-1 and TIMP-2 were expressed in the ductal plate and migrating primitive biliary cells. Trypsinogen/trypsin, chymotrypsinogen/chymotrypsin, and cathepsin B were also expressed in primitive biliary cells. These data suggest that MMP, trypsinogen/trypsin, chymotrypsinogen/chymotrypsin, and cathepsin B play a critical role in biliary cell migration during human intrahepatic bile duct development by degrading extracellular matrix proteins. The data also suggest that MMP inhibitors (TIMP-1 and TIMP-2) and MMP activators (trypsin, chymotrypsin, and cathepsin B) play an important role in biliary cell migration. The coordinated expression of MMP, MMP inhibitors, and MMP activators may be necessary for the normal development of human intrahepatic bile ducts.

Indexed as

Cell MovementEmbryonic and Fetal DevelopmentBile Ducts, IntrahepaticCathepsin BChymotrypsinogenGlycoproteinsHumansMetalloendopeptidasesProtease InhibitorsProteinsTissue Inhibitor of Metalloproteinase-2Tissue Inhibitor of MetalloproteinasesTrypsinogenCathepsin BChymotrypsinogenGlycoproteinsMetalloendopeptidasesProtease InhibitorsProteinsTissue Inhibitor of Metalloproteinase-2Tissue Inhibitor of MetalloproteinasesTrypsinogen

Identifiers

PMID7485384
PMCPMC1869511
OpenAlexW1647145872

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.