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通过组合方法增强δ9-四氢大麻酚在白血病细胞中的体外细胞毒性活性。

Enhancing the in vitro cytotoxic activity of Delta9-tetrahydrocannabinol in leukemic cells through a combinatorial approach.

作者信息

Liu Wai M, Scott Katherine A, Shamash Jonathan, Joel Simon, Powles Thomas B

机构信息

Department of Oncology, St George's University of London, Jenner Wing, London, UK.

出版信息

Leuk Lymphoma. 2008 Sep;49(9):1800-9. doi: 10.1080/10428190802239188.

Abstract

Delta(9)-Tetrahydrocannabinol (THC) is the active metabolite of cannabis, which has demonstrable cytotoxic activity in vitro. In support of our previously published data, we have investigated the interactions between THC and anti-leukemia therapies and studied the role of the signalling pathways in mediating these effects. Results showed clear synergistic interactions between THC and the cytotoxic agents in leukemic cells. Additionally, exposure of cells to sub lethal levels of THC (1 microM) sensitised cells to these cytotoxic agents, by reducing IC(50) values by approximately 50%. Sensitisation appeared to be dependent upon the ability of THC to down regulate phosphorylated ERK, as cells dominantly expressive of MEK were not sensitised to the cytotoxic drugs by equi-molar amounts of THC. Overall, these results demonstrate for the first time that a combination approach with THC and established cytotoxic agents may enhance cell death in vitro. Additionally the MAPK/ERK pathway appears responsible in part for these effects.

摘要

Δ⁹-四氢大麻酚(THC)是大麻的活性代谢产物,在体外具有明显的细胞毒性活性。为支持我们之前发表的数据,我们研究了THC与抗白血病疗法之间的相互作用,并研究了信号通路在介导这些效应中的作用。结果显示,THC与白血病细胞中的细胞毒性药物之间存在明显的协同相互作用。此外,将细胞暴露于亚致死水平的THC(1微摩尔)可使细胞对这些细胞毒性药物敏感,使半数抑制浓度(IC₅₀)值降低约50%。这种致敏作用似乎取决于THC下调磷酸化细胞外信号调节激酶(ERK)的能力,因为主要表达丝裂原活化蛋白激酶激酶(MEK)的细胞不会因等摩尔量的THC而对细胞毒性药物敏感。总体而言,这些结果首次证明,将THC与已有的细胞毒性药物联合使用的方法可能会增强体外细胞死亡。此外,丝裂原活化蛋白激酶/细胞外信号调节激酶(MAPK/ERK)通路似乎部分介导了这些效应。

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