Biomolecules & Therapeutics

  • 제21권1호
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  • Pages.29-34
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  • 2013
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  • 1976-9148(pISSN)
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  • 2005-4483(eISSN)
한국응용약물학회 (The Korean Society of Applied Pharmacology)
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Down-Regulation of Survivin by Nemadipine-A Sensitizes Cancer Cells to TRAIL-Induced Apoptosis

  • Park, Seong Ho (Ilsong Institute for Life Science, Hallym University) ;
  • Park, So Jung (Graduate School of East-West Medical Science, Kyung Hee University) ;
  • Kim, Joo-Oh (Graduate School of East-West Medical Science, Kyung Hee University) ;
  • Shin, Ji Hyun (Graduate School of East-West Medical Science, Kyung Hee University) ;
  • Kim, Eun Sung (Graduate School of East-West Medical Science, Kyung Hee University) ;
  • Jo, Yoon Kyung (Graduate School of East-West Medical Science, Kyung Hee University) ;
  • Kim, Jae-Sung (Division of Radiation Cancer Research, Korea Institute of Radiological and Medical Science) ;
  • Park, So Jung (Asan Institute for Life Science, Asan Medical Center) ;
  • Jin, Dong-Hoon (Asan Institute for Life Science, Asan Medical Center) ;
  • Hwang, Jung Jin (Asan Institute for Life Science, Asan Medical Center) ;
  • Lee, Seung Jin (Asan Institute for Life Science, Asan Medical Center) ;
  • Jeong, Seong-Yun (Asan Institute for Life Science, Asan Medical Center) ;
  • Lee, Chaeyoung (Department of Bioinformatics and Life Science, Soongsil University) ;
  • Kim, InKi (Asan Institute for Life Science, Asan Medical Center) ;
  • Cho, Dong-Hyung (Graduate School of East-West Medical Science, Kyung Hee University)
  • 투고 : 2012.11.09
  • 심사 : 2012.11.28
  • 발행 : 2013.01.31
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초록

The tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) is a member of the tumor necrosis factor family of cytokines. TRAIL selectively induces apoptotic cell death in various tumors and cancer cells, but it has little or no toxicity in normal cells. Agonism of TRAIL receptors has been considered to be a valuable cancer-therapeutic strategy. However, more than 85% of primary tumors are resistant to TRAIL, emphasizing the importance of investigating how to overcome TRAIL resistance. In this report, we have found that nemadipine-A, a cell-permeable L-type calcium channel inhibitor, sensitizes TRAIL-resistant cancer cells to this ligand. Combination treatments using TRAIL with nemadipine-A synergistically induced both the caspase cascade and apoptotic cell death, which were blocked by a pan caspase inhibitor (zVAD) but not by autophagy or a necrosis inhibitor. We further found that nemadipine-A, either alone or in combination with TRAIL, notably reduced the expression of survivin, an inhibitor of the apoptosis protein (IAP) family of proteins. Depletion of survivin by small RNA interference (siRNA) resulted in increased cell death and caspase activation by TRAIL treatment. These results suggest that nemadipine-A potentiates TRAIL-induced apoptosis by down-regulation of survivin expression in TRAIL resistant cells. Thus, combination of TRAIL with nemadipine-A may serve a new therapeutic scheme for the treatment of TRAIL resistant cancer cells, suggesting that a detailed study of this combination would be useful.

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참고문헌

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