Evidence map›Paper›PMID 10733585›Full record

ArticleMolecular and cellular biology2000

The DNA binding protein BTEB mediates acetaldehyde-induced, jun N-terminal kinase-dependent alphaI(I) collagen gene expression in rat hepatic stellate cells.

A Chen, B H Davis

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
9.0field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 83 citations in OpenAlex.

  1. Review
  2. Review
  3. miR-338-3p blocks TGFβ-induced myofibroblast differentiation through the induction of PTEN.American journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  4. Aldehyde Dehydrogenase, Liver Disease and Cancer.International journal of biological sciences · 2020
    Review
  5. Review
  6. Crosstalk of HNF4Acta pharmaceutica Sinica. B · 2016
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Targeting collagen expression in alcoholic liver disease.World journal of gastroenterology · 2011
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

A ChenGastroenterology Section, Department of Medicine, University of Chicago Medical Center, Chicago, IL 60637, USA.
B H Davis
University of Chicago Medical Center · US

Funding

ULTRASTRUCTURE AND CYTOMORPHOLOGY COREP30DK042086 · NIDDK · UNIVERSITY OF CHICAGO · PI ABADIE, VALERIE · 1990 to 2025
$29.8M
Research Training in Digestive Health, Diseases, and NutritionT32DK007074 · NIDDK · UNIVERSITY OF CHICAGO · PI EUGENE B CHANG · 1986 to 2026
$11.3M
REGULATION OF HEPATIC ITO CELL ACTIVATIONR01DK047995 · NIDDK · UNIVERSITY OF CHICAGO · PI CHEN, ANPING · 1995 to 2009
$2.1M
ROLES OF ACTIN AND MYOSIN IN PANCREATIC SECRETIONK08DK002022 · NIDDK · UNIVERSITY OF CHICAGO · PI BISSONNETTE, MARC · 1990 to 1995
–
REGULATION OF LIVER CELL FUNCTION DURING CIRRHOSISR29DK040223 · NIDDK · UNIVERSITY OF CHICAGO · PI DAVIS, BERNARD H · 1989 to 1993
–
NIDDK NIH HHS DK02022NIDDK NIH HHS DK40223NIDDK NIH HHS DK42086NIDDK NIH HHS P30 DK042086NIDDK NIH HHS R01 DK047995NIDDK NIH HHS T32 DK007074
6 · The paper itself

Abstract

Alcohol-induced cirrhosis results partially from the excessive production of collagen matrix proteins, which, predominantly alphaI(I) collagen, are produced and secreted by activated hepatic stellate cells (HSC). The accumulation of alphaI(I) collagen in HSC during cirrhosis is largely due to an increase in alphaI(I) collagen gene expression. Acetaldehyde, the major active metabolite of alcohol, is known to stimulate alphaI(I) collagen production in HSC. However, the mechanisms responsible for it remain unknown. The aim of this study was to elucidate the mechanisms by which alphaI(I) collagen gene expression is induced by acetaldehyde in rat HSC. In the present study, the acetaldehyde response element was located in a distal GC box, previously described as the UV response element, in the promoter of the alphaI(I) collagen gene (-1484 to -1476). The GC box was predominantly bound by the DNA binding transcription factor BTEB (basic transcription element binding protein), expression of which was acetaldehyde and UV inducible. Blocking BTEB protein expression significantly reduced the steady-state levels of the acetaldehyde-induced alphaI(I) collagen mRNA, suggesting that BTEB is required for this gene expression. Further studies found that acetaldehyde activated Jun N-terminal kinase (JNK) 1 and 2 and activator protein 1 (AP-1) transactivating activity. Inhibition of JNK activation resulted in the reduction of the acetaldehyde-induced BTEB protein abundance and alphaI(I) collagen mRNA levels, indicating that the expression of both genes is JNK dependent in HSC. Taken together, these studies demonstrate that BTEB mediates acetaldehyde-induced, JNK-dependent alphaI(I) collagen gene expression in HSC.

Indexed as

Gene Expression RegulationAcetaldehydeAnimalsCollagenConnective Tissue CellsDNA-Binding ProteinsJNK Mitogen-Activated Protein KinasesKruppel-Like Transcription FactorsLiverMaleMitogen-Activated Protein KinasesRatsRats, Sprague-DawleySignal TransductionTranscription FactorsZinc FingersAcetaldehydeCollagenDNA-Binding ProteinsJNK Mitogen-Activated Protein KinasesKlf9 protein, ratKruppel-Like Transcription FactorsMitogen-Activated Protein KinasesTranscription Factors

Identifiers

PMID10733585
PMCPMC85498
OpenAlexW2111052846

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.