1. Academic Validation
  2. Apo2L/TRAIL: apoptosis signaling, biology, and potential for cancer therapy

Apo2L/TRAIL: apoptosis signaling, biology, and potential for cancer therapy

  • Cytokine Growth Factor Rev. 2003 Jun-Aug;14(3-4):337-48. doi: 10.1016/s1359-6101(03)00029-7.
Alexandru Almasan 1 Avi Ashkenazi
Affiliations

Affiliation

  • 1 Department of Cancer Biology, Lerner Research Institute, The Cleveland Clinic Foundation, Cleveland, OH 44195, USA. almasaa@ccf.org
Abstract

Apo2 ligand or tumor necrosis factor (TNF)-related apoptosis-inducing ligand (Apo2L/TRAIL) is one of several members of the TNF gene superfamily that induce Apoptosis through engagement of death receptors. Apo2L/TRAIL is unusual as compared to any other cytokine as it interacts with a complex system of receptors: two pro-apoptotic death receptors and three anti-apoptotic decoys. This protein has generated tremendous excitement as a potential tumor-specific Cancer therapeutic because, as a stable soluble trimer, it selectively induces Apoptosis in many transformed cells but not in normal cells. Transcriptional activation of Apo2L/TRAIL by interferons (IFNs) through specific regulatory elements in its promoter, and possibly by a number of other cytokines, reveals its possible involvement in the activation of natural killer cells, cytotoxic T lymphocytes, and dendritic cells. In this review, we focus on the Apoptosis signaling pathways stimulated by Apo2L/TRAIL, summarize what is known to date about the physiological role of this ligand and the potential for its application to Cancer therapy.

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