A novel AP-1 element in the CD95 ligand promoter is required for induction of apoptosis in hepatocellular carcinoma cells upon treatment with anticancer drugs

The CD95 (also called APO-1 or Fas) system plays a major role in the induction of apoptosis in lymphoid and nonlymphoid tissues in response to a variety of extracellular signals, including chemotherapeutic drugs. Here we report that the CD95 ligand (CD95L) is upregulated in hepatoma cells upon treat...

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Bibliographic Details
Main Authors: Eichhorst, Sören (Author) , Li-Weber, Min (Author) , Schulze-Bergkamen, Henning (Author) , Angel, Peter (Author) , Krammer, Peter H. (Author)
Format: Article (Journal)
Language:English
Published: Oct. 2000
In: Molecular and cellular biology
Year: 2000, Volume: 20, Issue: 20, Pages: 7826-7837
ISSN:1098-5549
Online Access:Verlag, lizenzpflichtig, Volltext: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC86378/
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Author Notes:Sören T. Eichhorst, Martina Müller, Min Li-Weber, Henning Schulze-Bergkamen, Peter Angel, and Peter H. Krammer
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Summary:The CD95 (also called APO-1 or Fas) system plays a major role in the induction of apoptosis in lymphoid and nonlymphoid tissues in response to a variety of extracellular signals, including chemotherapeutic drugs. Here we report that the CD95 ligand (CD95L) is upregulated in hepatoma cells upon treatment with antineoplastic drugs. Upregulation by different chemotherapeutic drugs is functionally relevant for drug-induced apoptosis and is mediated by transcriptional mechanisms. The MEKK1/JNKK pathway and a novel AP-1 element in the CD95L promoter downstream of the TATA box are required for CD95L upregulation. Thus, understanding the mechanisms of CD95-mediated apoptosis through CD95L upregulation upon treatment of hepatocellular carcinomas with chemotherapeutic drugs may contribute to the improvement of anticancer chemotherapy.
Item Description:Gesehen am 26.04.2021
Physical Description:Online Resource
ISSN:1098-5549