髓系白血病
二甲双胍
mTORC1型
药理学
医学
癌症研究
化学
PI3K/AKT/mTOR通路
信号转导
内分泌学
糖尿病
生物化学
作者
Yuan Fang,Cong Cheng,Fei‐Yan Xiao,Hongcai Liu,Shan Cao,Gan Zhou
出处
期刊:Life Sciences
[Elsevier BV]
日期:2020-01-08
卷期号:243: 117276-117276
被引量:33
标识
DOI:10.1016/j.lfs.2020.117276
摘要
Chemo-resistance still was the main obstacle for AML patients, more effective and less toxic forms of therapies were desperately needed. Metformin, a classic hypoglycemic drug for diabetes recently delivered us a new identity that it exerted anti-tumor activity through suppressing mTOR in various tumors. But the anti-tumor effect of metformin in AML was not clear.In this study, we used CCK8 assay and apoptosis assay to determine the anti-leukemia activity of metformin combined with AraC, and explore the mechanism of the joint role of Ara-C/metformin in AML. We finally used xenograft experiment in mice to determine the anti-leukemia effect of Ara-C/metformin in vivo.We found that metformin could synergistically sensitize AML cells to Ara-C via inhibiting mTORC1/P70S6K pathway. In vivo experiment also verified metformin in aid of Ara-C caused an obviously synergistic anti-tumor effect.We firstly found the synergistic anti-tumor effect of Ara-C/metformin in AML through inhibiting mTORC1/P70S6K pathway.
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