废除热休克蛋白70的诱导作为一种增加热休克蛋白90抑制剂17-烯丙基氨基-去甲氧基格尔德霉素抗白血病活性的策略。
Abrogation of heat shock protein 70 induction as a strategy to increase antileukemia activity of heat shock protein 90 inhibitor 17-allylamino-demethoxy geldanamycin.
作者信息
Guo Fei, Rocha Kathy, Bali Purva, Pranpat Michael, Fiskus Warren, Boyapalle Sandhya, Kumaraswamy Sandhya, Balasis Maria, Greedy Benjamin, Armitage E Simon M, Lawrence Nicholas, Bhalla Kapil
机构信息
Department of Interdisciplinary Oncology, H. Lee Moffitt Cancer Center, Tampa, Florida 33612, USA.
出版信息
Cancer Res. 2005 Nov 15;65(22):10536-44. doi: 10.1158/0008-5472.CAN-05-1799.
17-Allylamino-demethoxy geldanamycin (17-AAG) inhibits the chaperone association of heat shock protein 90 (hsp90) with the heat shock factor-1 (HSF-1), which induces the mRNA and protein levels of hsp70. Increased hsp70 levels inhibit death receptor and mitochondria-initiated signaling for apoptosis. Here, we show that ectopic overexpression of hsp70 in human acute myelogenous leukemia HL-60 cells (HL-60/hsp70) and high endogenous hsp70 levels in Bcr-Abl-expressing cultured CML-BC K562 cells confers resistance to 17-AAG-induced apoptosis. In HL-60/hsp70 cells, hsp70 was bound to Bax, inhibited 17-AAG-mediated Bax conformation change and mitochondrial localization, thereby inhibiting the mitochondria-initiated events of apoptosis. Treatment with 17-AAG attenuated the levels of phospho-AKT, AKT, and c-Raf but increased hsp70 levels to a similar extent in the control HL-60/Neo and HL-60/hsp70 cells. Pretreatment with 17-AAG, which induced hsp70, inhibited 1-beta-D-arabinofuranosylcytosine or etoposide-induced apoptosis in HL-60 cells. Stable transfection of a small interfering RNA (siRNA) to hsp70 completely abrogated the endogenous levels of hsp70 and blocked 17-AAG-mediated hsp70 induction, resulting in sensitizing K562/siRNA-hsp70 cells to 17-AAG-induced apoptosis. This was associated with decreased binding of Bax to hsp70 and increased 17-AAG-induced Bax conformation change. 17-AAG-mediated decline in the levels of AKT, c-Raf, and Bcr-Abl was similar in K562 and K562/siRNA-hsp70 cells. Cotreatment with KNK437, a benzylidine lactam inhibitor of hsp70 induction and thermotolerance, attenuated 17-AAG-mediated hsp70 induction and increased 17-AAG-induced apoptosis and loss of clonogenic survival of HL-60 cells. Collectively, these data indicate that induction of hsp70 attenuates the apoptotic effects of 17-AAG, and abrogation of hsp70 induction significantly enhances the antileukemia activity of 17-AAG.
17-烯丙基氨基-去甲氧基格尔德霉素(17-AAG)抑制热休克蛋白90(hsp90)与热休克因子-1(HSF-1)的伴侣蛋白结合,从而诱导hsp70的mRNA和蛋白水平升高。hsp70水平升高会抑制死亡受体和线粒体启动的凋亡信号传导。在此,我们发现人急性髓性白血病HL-60细胞(HL-60/hsp70)中hsp70的异位过表达以及表达Bcr-Abl的培养慢性粒细胞白血病急变期K562细胞中内源性hsp70的高表达赋予了对17-AAG诱导凋亡的抗性。在HL-60/hsp70细胞中,hsp70与Bax结合,抑制17-AAG介导的Bax构象变化和线粒体定位,从而抑制凋亡的线粒体启动事件。用17-AAG处理可使对照HL-60/Neo和HL-60/hsp70细胞中的磷酸化AKT、AKT和c-Raf水平降低,但hsp70水平升高至相似程度。用诱导hsp70的17-AAG预处理可抑制1-β-D-阿拉伯呋喃糖基胞嘧啶或依托泊苷诱导的HL-60细胞凋亡。用小干扰RNA(siRNA)稳定转染hsp70可完全消除hsp70的内源性水平并阻断17-AAG介导的hsp70诱导,导致K562/siRNA-hsp70细胞对17-AAG诱导的凋亡敏感。这与Bax与hsp70的结合减少以及17-AAG诱导的Bax构象变化增加有关。17-AAG介导的AKT、c-Raf和Bcr-Abl水平下降在K562和K562/siRNA-hsp70细胞中相似。与KNK437(一种hsp70诱导和热耐受的苄叉内酰胺抑制剂)联合处理可减弱17-AAG介导的hsp70诱导,并增加17-AAG诱导的HL-60细胞凋亡和克隆形成存活能力的丧失。总体而言,这些数据表明hsp70的诱导减弱了17-AAG的凋亡作用,而hsp70诱导的消除显著增强了17-AAG的抗白血病活性。