Cited by 70TGF-β signaling in diseasesLiver physiology and pathologyCell death mechanisms and regulation

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Epidermal growth factor, but not hepatocyte growth factor, suppresses the apoptosis induced by transforming growth factor-beta in fetal hepatocytes in primary culture

Fabregat, Isabel, Sanchez, Aránzazu, Alvarez, Alberto M., Toshikazu Nakamura, Benito, Manuel·1996·FEBS Letters

Abstract

We studied whether the TGF‐β‐induced apoptosis in fetal hepatocyte primary cultures may be modulated by the presence of mitogenic stimuli, such as EGF or HGF. EGF prevented cell death, showing a dose dependence that was identical to that observed for its effect on DNA synthesis stimulation. HGF, in contrast, had no effect, even at high concentrations. EGF blocked apoptosis, since in the presence of this factor cells did not show DNA fragmentation. Moreover, EGF, but not HGF, blocked c‐fos induction associated with the apoptotic process induced by TGF‐β in these cells.

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References 26 · Cited by 70

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Metadata

Authors
Fabregat, I., Sanchez, A., Alvarez, A. M., Nakamura, T., & Benito, M.
Affiliations
  • Universidad Complutense de Madrid (ES)
  • The University of Osaka (JP)
Venue
FEBS Letters
Publisher
Wiley
Published
1996-04-08
Volume
384
Issue
1
Pages
14-18
ISSN
  • 0014-5793 (ISSN-L)
  • 1873-3468
OpenAlex
W2064759337
Cited by
70
References
26
Citations by year
2022: 1 · 2019: 1 · 2018: 1 · 2015: 2 · 2013: 1
FWCI
3.03
Type
journal article
Language
en
Open access
closed
Locations
  • FEBS Letters (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
  • Health Sciences › Medicine › Hepatology › Liver physiology and pathology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
Keywords
epidermal growth factor, hepatocyte growth factor, TGF-beta, apoptosis, fetal hepatocytes, c-fos induction, DNA fragmentation, mitogen stimulation, cell death inhibition
MeSH terms
Animals, Cell Nucleus, Cell Survival, Cells, Cultured, DNA, DNA Damage, Dose-Response Relationship, Drug, Epidermal Growth Factor, Fetus, Flow Cytometry, Liver, Transforming Growth Factor beta, Proto-Oncogene Proteins c-fos, Genes, fos, Rats, Wistar, Apoptosis, Hepatocyte Growth Factor, Rats

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