p53-dependent regulation of Mcl-1 contributes to synergistic cell death by ionizing radiation and the Bcl-2/Bcl-XL inhibitor ABT-737

Treatment with the Bcl-2/Bcl-XL inhibitor ABT-737 is a promising novel strategy to therapeutically induce apoptotic cell death in malignant tumors such as glioblastomas. Although many studies have demonstrated that ABT-737 acts synergistically with chemotherapeutic drugs, the possibility of a combin...

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Main Authors: Tagscherer, Katrin (Author) , Faßl, Anne (Author) , Sinkovic, Tabea (Author) , Combs, Stephanie (Author) , Roth, Wilfried (Author)
Format: Article (Journal)
Language:English
Published: 2012
In: Apoptosis
Year: 2012, Volume: 17, Issue: 2, Pages: 187-199
ISSN:1573-675X
DOI:10.1007/s10495-011-0664-3
Online Access:Verlag, Volltext: http://dx.doi.org/10.1007/s10495-011-0664-3
Verlag, Volltext: https://link.springer.com/article/10.1007/s10495-011-0664-3
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Author Notes:Katrin E. Tagscherer, Anne Fassl, Tabea Sinkovic, Stephanie E. Combs, Wilfried Roth
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Summary:Treatment with the Bcl-2/Bcl-XL inhibitor ABT-737 is a promising novel strategy to therapeutically induce apoptotic cell death in malignant tumors such as glioblastomas. Although many studies have demonstrated that ABT-737 acts synergistically with chemotherapeutic drugs, the possibility of a combined treatment with ionizing radiation (IR) and ABT-737 has not yet been thoroughly investigated. Similarly, the relationship between p53 function and the pro-apoptotic effects of ABT-737 are still obscure. Here, we demonstrate that IR and ABT-737 synergistically induce apoptosis in glioblastoma cells. The sensitivity to ABT-737-mediated cell death is significantly increased by the IR-dependent accumulation of cells in the G2/M cell cycle phase. Wild type p53 function inhibits the efficacy of a combined IR and ABT-737 treatment via a p21-dependent G1 cell cycle arrest. Moreover, mutant as well as wild type p53 counteract the pro-apoptotic activity of ABT-737 by maintaining the expression levels of the Mcl-1 protein. Thus, p53 regulates the sensitivity to ABT-737 of glioblastoma cells. Our results warrant a further evaluation of a novel combination therapy using IR and ABT-737. The efficacy of such a therapy could be substantially enhanced by Mcl-1-lowering strategies.
Item Description:Published online: 15 October 2011
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Physical Description:Online Resource
ISSN:1573-675X
DOI:10.1007/s10495-011-0664-3