机构:Sichuan Univ, W China Med Sch, Dept Hematol, Chengdu 610041, Sichuan Provinc, Peoples R China
Li, Jian
Zhang, Kaiji
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机构:Sichuan Univ, W China Med Sch, Dept Hematol, Chengdu 610041, Sichuan Provinc, Peoples R China
Zhang, Kaiji
Meng, Wentong
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机构:
Sichuan Univ, Lab Stem Cell Biol, State Key Lab Biotherapy, Chengdu 610041, Sichuan Provinc, Peoples R ChinaSichuan Univ, W China Med Sch, Dept Hematol, Chengdu 610041, Sichuan Provinc, Peoples R China
Meng, Wentong
[2
]
Yang, Yiming
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Sichuan Univ, W China Med Sch, Dept Hematol, Chengdu 610041, Sichuan Provinc, Peoples R ChinaSichuan Univ, W China Med Sch, Dept Hematol, Chengdu 610041, Sichuan Provinc, Peoples R China
Yang, Yiming
[1
]
机构:
[1] Sichuan Univ, W China Med Sch, Dept Hematol, Chengdu 610041, Sichuan Provinc, Peoples R China
[2] Sichuan Univ, Lab Stem Cell Biol, State Key Lab Biotherapy, Chengdu 610041, Sichuan Provinc, Peoples R China
Introduction: The prognosis of acute promyelocytic leukemia (APL) has been significantly improved by the use of all-trans retinoic acid (ATRA) and arsenic trioxide (ATO). However, the utility of these drugs is limited by resistance to ATRA and the side effects of ATO. It has been reported that Tanshinone IIA (Tan IIA), a diterpene quinone isolated from Salvia Miltiorrhiza Bunge, induces apoptosis in the APL cell line, NB4. The effect of Tan IIA on the ATRA-resistant APL cell line (MR2) is unknown. Methods: In this study, the effects of Tan IIA and ATO, alone and in combination, on MR2 cell apoptosis were investigated using transmission electron microscopy, flow cytom-etry and Western blot analyses. Results: Nuclear changes typical of apoptosis were observed in Tan IIA-treated MR2 cells. Apoptosis was shown to be induced in a dose-and time-dependent manner with the activation of caspase-3 resulting in upregulation of tumor necrosis factor-a expression, activation of caspase-8 and alteration in mitochondrial transmembrane potential with release of cytochrome c (cyto-c). Tan IIA and ATO acted synergistically on the induction of MR2 cell apoptosis. Conclusions: These data indicate that Tan IIA may be beneficial in the treatment of ATRA-resistant APL and in combination with ATO for APL therapy in the clinic.
机构:
George Washington Univ, Med Ctr, Div Hematol Oncol, Bone Marrow Transplant Program, Washington, DC 20037 USAGeorge Washington Univ, Med Ctr, Div Hematol Oncol, Bone Marrow Transplant Program, Washington, DC 20037 USA
Elbahesh, Ehab
Patel, Nihar
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George Washington Univ, Med Ctr, Div Hematol Oncol, Bone Marrow Transplant Program, Washington, DC 20037 USAGeorge Washington Univ, Med Ctr, Div Hematol Oncol, Bone Marrow Transplant Program, Washington, DC 20037 USA
Patel, Nihar
Tabbara, Imad A.
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George Washington Univ, Med Ctr, Div Hematol Oncol, Bone Marrow Transplant Program, Washington, DC 20037 USAGeorge Washington Univ, Med Ctr, Div Hematol Oncol, Bone Marrow Transplant Program, Washington, DC 20037 USA
机构:
Mem Sloan Kettering Canc Ctr, Leukemia Serv, New York, NY 10065 USA
Mem Sloan Kettering Canc Ctr, Weill Cornell Med Coll, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Leukemia Serv, New York, NY 10065 USA