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

Caspase-8 与粘着斑复合物的结合促进肿瘤细胞迁移和转移

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作者: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

Abstract

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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