Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Sci. STKE, 20 November 2007
Vol. 2007, Issue 413, p. tw421
[DOI: 10.1126/stke.4132007tw421]


Apoptosis Smac’d to Death

John F. Foley

Science’s STKE, AAAS, Washington, DC 20005, USA

Inhibitor of apoptosis (IAP) proteins bind, through their baculovirus IAP repeat (BIR) domains, to caspases, the proteases that mediate apoptosis, thus preventing apoptotic cell death. IAPs also contain RING domains and so act as E3 ubiquitin ligases that target proteins (and themselves) for proteasomal degradation. IAPs are more abundant in cancer cells than in normal cells, making IAPs attractive therapeutic targets. IAP activity is blocked by Smac (second mitochondrial activator of caspases), whose release from mitochondria is triggered by proapoptotic stimuli. Two groups have now designed and characterized mimetics of Smac. Varfolomeev et al. treated various cancer cell lines with their compounds, MV1 and BV6, and saw the rapid degradation of the IAP family members, c-IAP1 and c-IAP2, as assessed by Western blotting, which was blocked by an inhibitor of the proteasome. Both compounds also led to a dose-dependent increase in cell death, which was blocked by the caspase inhibitor z-VAD. Blockade of tumor necrosis factor-{alpha} (TNF-{alpha}) inhibited BV6-mediated apoptosis, as did a small interfering (si) RNA against the TNF-{alpha} receptor (TNFR1). Vince et al. found similar results when characterizing their IAP antagonist compounds. TNF-{alpha} production is characteristic of nuclear factor {kappa}B (NF-{kappa}B) activation. Both groups showed that the canonical and noncanonical NF-{kappa}B pathways were activated in cells in which IAPs were antagonized. NIK (NF-{kappa}B-inducing kinase), an activator of the noncanonical pathway, was constitutively bound to IAPs and then degraded, which was prevented by treatment with the Smac mimetics. Apoptosis mediated by these compounds was blocked by inhibitors of NF-{kappa}B. IAP antagonism also increased the recruitment to the TNFR1 of the kinase receptor-interacting protein 1 (RIP1), which is important for canonical NF-{kappa}B activation. Together these studies show that rather than simply interfering with the ability of IAPs to bind to caspases, Smac mimetics trigger IAP degradation, which has a twofold outcome. First, caspases are now uninhibited and responsive to a proapoptotic signal. Second, IAP degradation removes a block to noncanonical NF-{kappa}B activation, leading to the production of TNF-{alpha} that acts in an autocrine fashion to trigger cell death. Wu et al. discuss the potential use of these compounds in anticancer therapies.

E. Varfolomeev, J. W. Blankenship, S. M. Wayson, A. V. Fedorova, N. Kayagaki, P. Garg, K. Zobel, J. N. Dynek, L. O. Elliott, H. J. A. Wallweber, J. A. Flygare, W. J. Fairbrother, K. Deshayes, V. M. Dixit, D. Vucic, IAP antagonists induce autoubiquitination of c-IAPs, NF-{kappa}B activation, and TNF{alpha}-dependent apoptosis. Cell 131, 669-681 (2007). [Online Journal]

J. E. Vince, W. W.-L. Wong, N. Khan, R. Feltham, D. Chau, A. U. Ahmed, C. A. Benetatos, S. K. Chunduru, S. M. Condon, M. McKinlay, R. Brink, M. Leverkus, V. Tergaonkar, P. Schneider, B. A. Callus, F. Koentgen, D. L. Vaux, J. Silke, IAP antagonists target cIAP1 to induce TNF{alpha}-dependent apoptosis. Cell 131, 682-693 (2007). [Online Journal]

H. Wu, J. Tschopp, S.-C. Lin, Smac mimetics and TNF{alpha}: A dangerous liaison? Cell 131, 655-658 (2007). [Online Journal]

Citation: J. F. Foley, Smac’d to Death. Sci. STKE 2007, tw421 (2007).

To Advertise     Find Products

Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882