共 20 条
Inhibition of adenosine monophosphate-activated protein kinase induces apoptosis in multiple myeloma cells
被引:37
作者:

Baumann, Philipp
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机构:
Klinikum Univ Munchen, Med Klin Innenstadt, Dept Hematol & Oncol, D-80336 Munich, Germany Klinikum Univ Munchen, Med Klin Innenstadt, Dept Hematol & Oncol, D-80336 Munich, Germany

Mandl-Weber, Sonja
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h-index: 0
机构:
Klinikum Univ Munchen, Med Klin Innenstadt, Dept Hematol & Oncol, D-80336 Munich, Germany Klinikum Univ Munchen, Med Klin Innenstadt, Dept Hematol & Oncol, D-80336 Munich, Germany

Emmerich, Bertold
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机构:
Klinikum Univ Munchen, Med Klin Innenstadt, Dept Hematol & Oncol, D-80336 Munich, Germany Klinikum Univ Munchen, Med Klin Innenstadt, Dept Hematol & Oncol, D-80336 Munich, Germany

Straka, Christian
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h-index: 0
机构:
Klinikum Univ Munchen, Med Klin Innenstadt, Dept Hematol & Oncol, D-80336 Munich, Germany Klinikum Univ Munchen, Med Klin Innenstadt, Dept Hematol & Oncol, D-80336 Munich, Germany

Schmidmaier, Ralf
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机构:
Klinikum Univ Munchen, Med Klin Innenstadt, Dept Hematol & Oncol, D-80336 Munich, Germany Klinikum Univ Munchen, Med Klin Innenstadt, Dept Hematol & Oncol, D-80336 Munich, Germany
机构:
[1] Klinikum Univ Munchen, Med Klin Innenstadt, Dept Hematol & Oncol, D-80336 Munich, Germany
关键词:
adenosine monophosphate-activated protein kinase;
Bcl-xL;
Mcl-1;
multiple myeloma;
D O I:
10.1097/CAD.0b013e32801416b6
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
In this study, we show that adenosine monophosphate-activated protein kinase (AMPK) is expressed and activated in multiple myeloma cells. The inhibition of AMPK induced growth arrest and reduction of cell viability in the cell viability assay using the water-soluble tetrazolium salt 4-[3-(4-iodophenyl)-2-(4-nitrophenyl)-2H-5-tetrazolio]-1,3-benzene disulfonate (WST-1 assay). Induction of apoptosis was determined by annexin-V and propidium iodide staining. The prevention of apoptosis using the pancaspase inhibitor ZVAD-fmk and caspase-3 cleavage upon incubation with the AMPK inhibitor (AMPKI) is shown. Furthermore, incubation of myeloma cells with AMPKI resulted in the downregulation of pAMPK, Mcl-1 and Bcl-X(L)Coincubation of AMPKI and melphalan led to a strong additional increase of apoptosis in myeloma cells. We conclude that AMPKI has a strong antimyeloma activity in vitro and represents a new targeted strategy in the treatment of multiple myeloma.
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收藏
页码:405 / 410
页数:6
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