Ikeda T, Kimura F, Nakata Y, Sato K, Ogura K, Motoyoshi K, Sporn M, Kufe D
Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.
Cell Death Differ. 2005 May;12(5):523-31. doi: 10.1038/sj.cdd.4401574.
The triterpenoid 2-cyano-3,12-dioxooleana-1,9-dien-28-oic acid (CDDO) induces differentiation and apoptosis of diverse human tumor cells. In the present study, we examined the effects of the CDDO imidazolide imide (CDDO-Im) on the NB4 acute promyelocytic leukemia (APL) cell line and primary APL cells. The results show that CDDO-Im selectively downregulates expression of the PML/retinoic receptor alpha fusion protein by a caspase-dependent mechanism and sensitizes APL cells to the differentiating effects of all-trans retinoic acid (ATRA). CDDO-Im treatment of APL cells was also associated with disruption of redox balance and activation of the extrinsic apoptotic pathway. In concert with these results, CDDO-Im sensitizes APL cells to arsenic trioxide (ATO)-induced apoptosis. Our findings indicate that CDDO-Im may be effective in the treatment of APL by: (i) downregulation of PML/RARalpha; (ii) enhancement of ATRA-induced differentiation; and (iii) sensitization of ATO-induced APL cell death.
三萜类化合物2-氰基-3,12-二氧代齐墩果-1,9-二烯-28-酸(CDDO)可诱导多种人类肿瘤细胞分化并凋亡。在本研究中,我们检测了CDDO咪唑啉酰胺(CDDO-Im)对NB4急性早幼粒细胞白血病(APL)细胞系及原代APL细胞的影响。结果显示,CDDO-Im通过半胱天冬酶依赖性机制选择性下调早幼粒细胞白血病蛋白(PML)/维甲酸受体α融合蛋白的表达,并使APL细胞对全反式维甲酸(ATRA)的分化作用敏感。用CDDO-Im处理APL细胞还与氧化还原平衡的破坏及外源性凋亡途径的激活有关。与这些结果一致,CDDO-Im使APL细胞对三氧化二砷(ATO)诱导的凋亡敏感。我们的研究结果表明,CDDO-Im可能通过以下方式有效治疗APL:(i)下调PML/维甲酸受体α(PML/RARα);(ii)增强ATRA诱导的分化;(iii)使ATO诱导的APL细胞死亡敏感化。