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Induction of Apoptosis by Tosyl-JM3 in HL-60 cells
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  • Induction of Apoptosis by Tosyl-JM3 in HL-60 cells
  • Induction of Apoptosis by Tosyl-JM3 in HL-60 cells
저자명
Kim. Kun-Jung,Ju. Sung-Min,Lee. Chai-Ho,Kim. Won-Sin,Yun. Yong-Gab,Jeong. Han-Sol,Kim. Sung-Hoon,Park. Sung-Joo,Jeon. Byung-Hun
간행물명
동의생리병리학회지
권/호정보
2005년|19권 5호|pp.1370-1374 (5 pages)
발행정보
대한동의생리학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

The Tosyl-JM3 (TJM3) is a modified compound from one of 1,2,3,4-Tetra- hydroisoquinoline (THIQ) derivatives. The THIQs include potent cytotoxic agents that display a range of anti-tumor activities, antimicrobial activity, and other biological properties. In this study, we investigated the effect of TJM3 on the cytotoxicity, induction of apoptosis in human promyelocytic leukemia cells (HL-60 cells). TJM3 showed a significant cytotoxic activity in HL-60 cells (IC50 = approximately $60{mu}g/m{ell}$) after a 24 hr incubation. Treatment of HL-60 cells with TJM3 exhibited several features of apoptosis, including formation of DNA ladders in agarose gel electrophoresis, morphological changes of HL-60 cells with DAPI stain. Here we observed that TJM3 caused a decrease of procaspase-3 protein. Further molecular analysis demonstrated that TJM3 led to cleavage of poly(ADP-ribose) polymerase (PARP) by western blot and increase of hypodiploid (Sub-G1) population in the flow cytometric analysis. In conclusion, these above results indicate that TJM3 dramatically suppresses HL-60 cell growth and induces apoptosis. These data may support a possibility for the use of TJM3 in the prevention and treatment of leukemia.