Chen Chun, Zhuang Yingting, Chen Xianling, Chen Xiaole, Li Ding, Fan Yingjuan, Xu Jianhua, Chen Yuanzhong, Wu Lixian
Deptartment of Pharmacology, School of Pharmacy, Fujian Medical University (FMU), Fuzhou, China.
Institute of Materia Medica, School of Pharmacy, Fujian Medical University (FMU), Fuzhou, China.
Oncotarget. 2017 Feb 7;8(6):10025-10036. doi: 10.18632/oncotarget.14324.
Heat shock protein 90 (Hsp90) contains amino (N)-terminal domain, carboxyl(C)-terminal domain, and middle domains, which activate Hsp90 chaperone function cooperatively in tumor cells. One terminal occupancy might influence another terminal binding with inhibitor. The Bcr-Abl kinase is one of the Hsp90 clients implicated in the pathogenesis of chronic myeloid leukemia (CML). Present studies demonstrate that double inhibition of the N- and C-terminal termini can disrupt Hsp90 chaperone function synergistically, but not antagonistically, in Bcr-Abl-positive human leukemia cells. Furthermore, both the N-terminal inhibitor 17-AAG and the C-terminal inhibitor cisplatin (CP) have the capacity to suppress progenitor cells; however, only CP is able to inhibit leukemia stem cells (LSCs) significantly, which implies that the combinational treatment is able to suppress human leukemia in different mature states.
热休克蛋白90(Hsp90)包含氨基(N)末端结构域、羧基(C)末端结构域和中间结构域,这些结构域在肿瘤细胞中协同激活Hsp90伴侣功能。一个末端的占据可能会影响另一个末端与抑制剂的结合。Bcr-Abl激酶是参与慢性髓性白血病(CML)发病机制的Hsp90客户蛋白之一。目前的研究表明,在Bcr-Abl阳性的人类白血病细胞中,对N末端和C末端的双重抑制可协同而非拮抗地破坏Hsp90伴侣功能。此外,N末端抑制剂17-AAG和C末端抑制剂顺铂(CP)都有抑制祖细胞的能力;然而,只有CP能够显著抑制白血病干细胞(LSC),这意味着联合治疗能够抑制不同成熟状态的人类白血病。