Caspase-8 association with the focal adhesion complex promotes tumor cell migration and metastasis.

نویسندگان

  • Simone Barbero
  • Ainhoa Mielgo
  • Vicente Torres
  • Tal Teitz
  • David J Shields
  • David Mikolon
  • Matthew Bogyo
  • Daniela Barilà
  • Jill M Lahti
  • David Schlaepfer
  • Dwayne G Stupack
چکیده

Caspase-8 is a proapoptotic protease that suppresses neuroblastoma metastasis by inducing programmed cell death. Paradoxically, caspase-8 can also promote cell migration among nonapoptotic cells; here, we show that caspase-8 can promote metastasis when apoptosis is compromised. Migration is enhanced by caspase-8 recruitment to the cellular migration machinery following integrin ligation. Caspase-8 catalytic activity is not required for caspase-8-enhanced cell migration; rather, caspase-8 interacts with a multiprotein complex that can include focal adhesion kinase and calpain 2 (CPN2), enhancing cleavage of focal adhesion substrates and cell migration. Caspase-8 association with CPN2/calpastatin disrupts calpastatin-mediated inhibition of CPN2. In vivo, knockdown of either caspase-8 or CPN2 disrupts metastasis among apoptosis-resistant tumors. This unexpected molecular collaboration provides an explanation for the continued or elevated expression of caspase-8 observed in many tumors.

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عنوان ژورنال:
  • Cancer research

دوره 69 9  شماره 

صفحات  -

تاریخ انتشار 2009