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PMID: 26720004 Published · epublish English

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

PloS one ·Vol. 10 ·No. 12 ·2016-06-28

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

Abstract

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.

Article Info
Journal
PloS one
Abbr.
PLoS One
Published
2016-06-28
Indexed
2016-01-01
Updated
2016-11-26
Language
English
Country/Region
United States
NLM ID
101285081
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