Department of Medical Genetic Engineering, School of Medicine, Keimyung University, Dalseo-Gu, Daegu 704-701, Republic of Korea.
Oncol Rep. 2012 Dec;28(6):2227-32. doi: 10.3892/or.2012.2026. Epub 2012 Sep 12.
Evidence suggests that mistletoe extract has the potential to be used as an anticancer agent. Abnobaviscum F® is a European mistletoe extract from the host tree Fraxinus. We investigated the effect of Abnobaviscum F on the growth and survival of different leukemia cell lines. Abnobaviscum F treatment strongly reduced survival and induced apoptosis of K562 (human myeloid leukemia), RPMI-8226 (human plasmacytoma) and L1210 (murine lymphocytic leukemia) cells in culture. Using K562 cells to further investigate the mechanism of action of Abnobaviscum F, we showed that Abnobaviscum F-induced cell death was associated with the activation of caspase-9, JNK-1/2 and p38 MAPK, as well as with the downregulation of Mcl-1, and inhibition of ERK-1/2 and PKB phosphorylation. Moreover, Abnobaviscum F treatment led to both a reduction of cellular glutathione (GSH) and the induction of ER stress (GRP78 and CHOP induction and eIF-2α phosphorylation). By contrast, Abnobaviscum F did not impact the expression of the DR4 and DR5 death receptors. The Abnobaviscum F-induced apoptosis of K562 cells was blocked by pretreatment with either GSH, z-VAD-fmk or SP600125. Our results, therefore, show that Abnobaviscum F induces apoptosis of K562 cells through the activation of the intrinsic caspase pathway, the phosphorylation of JNK-1, the reduction of cellular GSH, and the induction of ER stress.
有证据表明,槲寄生提取物有可能被用作抗癌剂。Abnobaviscum®F 是一种源自宿主树 Fraxinus 的欧洲槲寄生提取物。我们研究了 Abnobaviscum®F 对不同白血病细胞系生长和存活的影响。Abnobaviscum®F 处理强烈降低了培养中的 K562(人髓性白血病)、RPMI-8226(人浆细胞瘤)和 L1210(鼠淋巴细胞白血病)细胞的存活率并诱导其凋亡。使用 K562 细胞进一步研究 Abnobaviscum®F 的作用机制,我们表明 Abnobaviscum®F 诱导的细胞死亡与 caspase-9、JNK-1/2 和 p38 MAPK 的激活以及 Mcl-1 的下调以及 ERK-1/2 和 PKB 磷酸化的抑制有关。此外,Abnobaviscum®F 处理导致细胞谷胱甘肽 (GSH) 的减少和内质网应激 (GRP78 和 CHOP 诱导和 eIF-2α 磷酸化) 的诱导。相比之下,Abnobaviscum®F 不影响 DR4 和 DR5 死亡受体的表达。K562 细胞的 Abnobaviscum®F 诱导的细胞凋亡被 GSH、z-VAD-fmk 或 SP600125 的预处理阻断。因此,我们的结果表明,Abnobaviscum®F 通过激活内在的半胱天冬酶途径、JNK-1 的磷酸化、细胞 GSH 的减少和内质网应激的诱导来诱导 K562 细胞的凋亡。