The XIAP inhibitor embelin sensitises malignant rhabdoid tumour cells to TRAIL treatment via enhanced activation of the extrinsic apoptotic pathway

  • Authors:
    • Rachel Coyle
    • Karen Slattery
    • Leanne Ennis
    • Maureen J. O'sullivan
    • Daniela M. Zisterer
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  • Published online on: May 20, 2019     https://doi.org/10.3892/ijo.2019.4804
  • Pages: 191-202
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Abstract

Malignant rhabdoid tumour (MRT) is a rare, aggressive paediatric neoplasm, primarily diagnosed in those below the age of three. MRTs most commonly arise in the central nervous system and kidneys. A poor prognosis accompanies the MRT diagnosis, with a reported 2‑year survival rate of 30%. Thus, there is an urgent need for the development of new therapies for this malignancy. Members of the inhibitor of apoptosis protein (IAP) family have previously been reported to be overexpressed in various cancers. As such, small molecule inhibitors of these family members have entered clinical trials. However, the role of IAPs in MRT has not been examined yet. The present study is the first report of the expression of a range of IAPs, including X‑linked inhibitor of apoptosis (XIAP), cellular inhibitor of apoptosis protein 1 (cIAP1), cellular inhibitor of apoptosis protein 2 (cIAP2), livin and survivin in MRT cell lines. Furthermore, the results demonstrated the ability of the XIAP inhibitor, embelin, to sensitise MRT cell lines to TNF‑related apoptosis‑inducing ligand (TRAIL) treatment. The enhanced cell death detected upon cotreatment was dependent on caspase‑8 and co‑occurred with caspase‑8 and caspase‑3 cleavage, suggesting engagement of the extrinsic apoptotic pathway. Sensitisation to TRAIL was accompanied by livin cleavage, alongside downregulation of survivin and the caspase‑8 inhibitor FLIPL. In addition, knockdown of XIAP using siRNA enhanced TRAIL‑mediated cell death, suggesting that this process may in part mediate sensitisation. In conclusion, the present results suggested that IAP inhibition may present a novel avenue for the treatment of MRT.
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July-2019
Volume 55 Issue 1

Print ISSN: 1019-6439
Online ISSN:1791-2423

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Spandidos Publications style
Coyle R, Slattery K, Ennis L, O'sullivan MJ and Zisterer DM: The XIAP inhibitor embelin sensitises malignant rhabdoid tumour cells to TRAIL treatment via enhanced activation of the extrinsic apoptotic pathway. Int J Oncol 55: 191-202, 2019.
APA
Coyle, R., Slattery, K., Ennis, L., O'sullivan, M.J., & Zisterer, D.M. (2019). The XIAP inhibitor embelin sensitises malignant rhabdoid tumour cells to TRAIL treatment via enhanced activation of the extrinsic apoptotic pathway. International Journal of Oncology, 55, 191-202. https://doi.org/10.3892/ijo.2019.4804
MLA
Coyle, R., Slattery, K., Ennis, L., O'sullivan, M. J., Zisterer, D. M."The XIAP inhibitor embelin sensitises malignant rhabdoid tumour cells to TRAIL treatment via enhanced activation of the extrinsic apoptotic pathway". International Journal of Oncology 55.1 (2019): 191-202.
Chicago
Coyle, R., Slattery, K., Ennis, L., O'sullivan, M. J., Zisterer, D. M."The XIAP inhibitor embelin sensitises malignant rhabdoid tumour cells to TRAIL treatment via enhanced activation of the extrinsic apoptotic pathway". International Journal of Oncology 55, no. 1 (2019): 191-202. https://doi.org/10.3892/ijo.2019.4804