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首页> 外文期刊>臨床血液 >The anti-tumoral effect of PI3K inhibitor and MEK inhibitor combined with STI571 on chronic myeloid leukemia cells in a bone marrow stromal cell co-culture system
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The anti-tumoral effect of PI3K inhibitor and MEK inhibitor combined with STI571 on chronic myeloid leukemia cells in a bone marrow stromal cell co-culture system

机译:PI3K抑制剂和MEK抑制剂与STI571联合STI571对骨髓基质细胞共培养系统慢性骨髓白血病细胞的抗肿瘤作用

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摘要

The goal of this study was to elucidate the functional roles of PI3K/AKT and MEK/ERK signaling on the proliferation and apoptosis of STI571-sensitive and -resistant CML cell lines in a co-culture system with human marrow stromal cells (MSCs), mimicking the bone marrow microenvironment. The phosphorylation of AKT and ERK was enhanced by co-culture with MSCs in both STI571-sensitive KBM-5 and STI571-resistant KBM-5/STI cells. In KBM-5 cells, the STI571 and PI3K inhibitor LY294002 combination was effective on apoptosis induction in the MSC co-culture system. In KBM-5/STI cells, treatment with LY294002 or PD98059 alone resulted in massive apoptosis, which was enhanced by co-culture with MSCs. These results provide a rationale for multi-molecular target therapy approaches based on a combination of signal transduction inhibitors with STI571 in CML.
机译:本研究的目的是阐明PI3K / AKT和MEK / ERK信号传导对具有人骨髓基质细胞(MSC)的共培养系统中ST571敏感和 - 敏感CML细胞系的增殖和凋亡的功能作用。 模仿骨髓微环境。 通过STI571敏感的KBM-5和STI571抗性KBM-5 / STI细胞中的MSCs与MSCs的共培养增强了AKT和ERK的磷酸化。 在KBM-5细胞中,STI571和PI3K抑制剂LY294002组合对MSC共培养系统中的凋亡诱导有效。 在KBM-5 / STI细胞中,单独用Ly294002或PD98059治疗导致大规模的凋亡,通过使用MSCs的共培养增强。 这些结果为多分子靶治疗方法提供了基于CML中STI571的信号转导抑制剂的组合的基本原理。

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