A Dual Role of Caspase-8 in Triggering and Sensing Proliferation-Associated DNA Damage, a Key Determinant of Liver Cancer Development

نویسندگان

  • Yannick Boege
  • Mohsen Malehmir
  • Marc E. Healy
  • Kira Bettermann
  • Anna Lorentzen
  • Mihael Vucur
  • Akshay K. Ahuja
  • Friederike Böhm
  • Joachim C. Mertens
  • Yutaka Shimizu
  • Lukas Frick
  • Caroline Remouchamps
  • Karun Mutreja
  • Thilo Kähne
  • Devakumar Sundaravinayagam
  • Monika J. Wolf
  • Hubert Rehrauer
  • Christiane Koppe
  • Tobias Speicher
  • Susagna Padrissa-Altés
  • Renaud Maire
  • Jörn M. Schattenberg
  • Ju-Seong Jeong
  • Lei Liu
  • Stefan Zwirner
  • Regina Boger
  • Norbert Hüser
  • Roger J. Davis
  • Beat Müllhaupt
  • Holger Moch
  • Henning Schulze-Bergkamen
  • Pierre-Alain Clavien
  • Sabine Werner
  • Lubor Borsig
  • Sanjiv A. Luther
  • Philipp J. Jost
  • Ricardo Weinlich
  • Kristian Unger
  • Axel Behrens
  • Laura Hillert
  • Christopher Dillon
  • Michela Di Virgilio
  • David Wallach
  • Emmanuel Dejardin
  • Lars Zender
  • Michael Naumann
  • Henning Walczak
  • Douglas R. Green
  • Massimo Lopes
  • Inna Lavrik
  • Tom Luedde
  • Mathias Heikenwalder
  • Achim Weber
چکیده

Concomitant hepatocyte apoptosis and regeneration is a hallmark of chronic liver diseases (CLDs) predisposing to hepatocellular carcinoma (HCC). Here, we mechanistically link caspase-8-dependent apoptosis to HCC development via proliferation- and replication-associated DNA damage. Proliferation-associated replication stress, DNA damage, and genetic instability are detectable in CLDs before any neoplastic changes occur. Accumulated levels of hepatocyte apoptosis determine and predict subsequent hepatocarcinogenesis. Proliferation-associated DNA damage is sensed by a complex comprising caspase-8, FADD, c-FLIP, and a kinase-dependent function of RIPK1. This platform requires a non-apoptotic function of caspase-8, but no caspase-3 or caspase-8 cleavage. It may represent a DNA damage-sensing mechanism in hepatocytes that can act via JNK and subsequent phosphorylation of the histone variant H2AX.

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عنوان ژورنال:

دوره 32  شماره 

صفحات  -

تاریخ انتشار 2017