PLoS ONE (Jan 2015)

Bay 61-3606 Sensitizes TRAIL-Induced Apoptosis by Downregulating Mcl-1 in Breast Cancer Cells.

  • So-Young Kim,
  • Sang Eun Park,
  • Sang-Mi Shim,
  • Sojung Park,
  • Kyung Kon Kim,
  • Seong-Yun Jeong,
  • Eun Kyung Choi,
  • Jung Jin Hwang,
  • Dong-Hoon Jin,
  • Christopher Doosoon Chung,
  • Inki Kim

DOI
https://doi.org/10.1371/journal.pone.0146073
Journal volume & issue
Vol. 10, no. 12
p. e0146073

Abstract

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Breast cancer cells generally develop resistance to TNF-Related Apoptosis-Inducing Ligand (TRAIL) and, therefore, assistance from sensitizers is required. In our study, we have demonstrated that Spleen tyrosine kinase (Syk) inhibitor Bay 61-3606 was identified as a TRAIL sensitizer. Amplification of TRAIL-induced apoptosis by Bay 61-3606 was accompanied by the strong activation of Bak, caspases, and DNA fragmentation. In mechanism of action, Bay 61-3606 sensitized cells to TRAIL via two mechanisms regulating myeloid cell leukemia sequence-1 (Mcl-1). First, Bay 61-3606 triggered ubiquitin-dependent degradation of Mcl-1 by regulating Mcl-1 phosphorylation. Second, Bay 61-3606 downregulates Mcl-1 expression at the transcription level. In this context, Bay 61-3606 acted as an inhibitor of Cyclin-Dependent Kinase (CDK) 9 rather than Syk. In summary, Bay 61-3606 downregulates Mcl-1 expression in breast cancer cells and sensitizes cancer cells to TRAIL-mediated apoptosis.