Department of Clinical Korean Medicine, Graduate School, Kyung Hee University, Seoul 02447, Republic of Korea.
Oncol Rep. 2018 Mar;39(3):1141-1147. doi: 10.3892/or.2018.6179. Epub 2018 Jan 3.
Rhus verniciflua Stokes has been widely used as a traditional medicinal plant with a variety of pharmacological activities. We investigated the mechanisms involved in mediating the effects of Rhus verniciflua Strokes (R. verniciflua) extract in human chronic myelogenous leukemia K562 cells, including caspase-dependent apoptotic pathways related to cell-cycle arrest, as well as the inhibition of nuclear factor NF-κB activation and upregulation of the mitogen-activated protein kinase (MAPK) signaling pathway. R. verniciflua extract suppressed the abnormal cellular proliferation of K562 cells in a dose- and time‑dependent manner and increased the quantitative proportions of cells involved in the early and late process of apoptosis. Furthermore, R. verniciflua extract significantly mediated the mRNA levels of pro-apoptotic and anti-apoptotic regulators, such as Bcl-2, Bax, Mcl-1 and survivin in apoptotic cells. Particularly, the treatment of K562 cells with R. verniciflua extract augmented the caspase‑3 activity and increased the expression of caspase‑3 protein, while co-treatment with R. verniciflua extract and the permeant pan‑caspase inhibitor Z-VAD-FMK and caspase‑3 inhibitor Z-DEVD-FMK inversely enhanced the proliferation of K562 cells. The extract of R. verniciflua inhibited the activation of NF-κB and the phosphorylation of ERK. Collectively, these results indicated that the extract of R. verniciflua inhibited the proliferation of human chronic myelogenous leukemia K562 cells by activating the apoptotic process via caspase‑3 overexpression and the regulation of the NF-κB and MAPK signaling.
漆树已被广泛用作具有多种药理活性的传统药用植物。我们研究了漆树提取物介导其对人慢性髓系白血病 K562 细胞作用的机制,包括与细胞周期停滞相关的半胱天冬酶依赖性凋亡途径,以及核因子 NF-κB 激活的抑制和丝裂原激活蛋白激酶(MAPK)信号通路的上调。漆树提取物以剂量和时间依赖的方式抑制 K562 细胞的异常细胞增殖,并增加参与细胞凋亡早期和晚期过程的细胞定量比例。此外,漆树提取物显著调节凋亡细胞中促凋亡和抗凋亡调节剂的 mRNA 水平,如 Bcl-2、Bax、Mcl-1 和 survivin。特别是,用漆树提取物处理 K562 细胞可增强 caspase-3 活性并增加 caspase-3 蛋白的表达,而同时用漆树提取物和通透型 pan-caspase 抑制剂 Z-VAD-FMK 和 caspase-3 抑制剂 Z-DEVD-FMK 处理则可逆转增强 K562 细胞的增殖。漆树提取物抑制 NF-κB 的激活和 ERK 的磷酸化。总之,这些结果表明,漆树提取物通过 caspase-3 过表达和 NF-κB 和 MAPK 信号通路的调节来激活凋亡过程,从而抑制人慢性髓系白血病 K562 细胞的增殖。