Stellrecht Christine M, Chen Lisa S, Ayres Mary L, Dennison Jennifer B, Shentu Shujun, Chen Yuling, Keating Michael J, Wierda William G, Gandhi Varsha
Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
The University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, TX, USA.
Br J Haematol. 2017 Oct;179(2):266-271. doi: 10.1111/bjh.14859. Epub 2017 Jul 24.
8-chloro-adenosine (8-Cl-Ado) is currently in phase-I clinical trials for acute myeloid leukaemia and chronic lymphocytic leukaemia (CLL). Previously, we demonstrated that treatment with 8-Cl-Ado leads to diminished ATP levels. We hypothesized that AMP-activated protein kinase (AMPK) signalling would be initiated in these cells, leading to induction of autophagy. AMPK activation and induction of autophagy were demonstrated during preclinical incubations in CLL cells with the analogues. Importantly, we extended similar observations in CLL lymphocytes during an 8-Cl-Ado phase-I trial. In conclusion, 8-Cl-Ado treatment induces autophagy in CLL lymphocytes in vitro as well as in vivo during clinical trial.
8-氯腺苷(8-Cl-Ado)目前正处于针对急性髓性白血病和慢性淋巴细胞白血病(CLL)的I期临床试验阶段。此前,我们证明用8-Cl-Ado治疗会导致ATP水平降低。我们推测在这些细胞中会启动AMP激活的蛋白激酶(AMPK)信号传导,从而导致自噬的诱导。在CLL细胞与类似物的临床前孵育过程中证实了AMPK激活和自噬诱导。重要的是,我们在8-Cl-Ado的I期试验期间对CLL淋巴细胞进行了类似的观察。总之,8-Cl-Ado治疗在体外以及临床试验期间的体内均可诱导CLL淋巴细胞发生自噬。