Pan Li-Long, Wang Xi-Ling, Luo Xiao-Ling, Liu Si-Yu, Xu Peng, Hu Jin-Feng, Liu Xin-Hua
1 Fudan University, Shanghai, China.
Integr Cancer Ther. 2017 Sep;16(3):351-359. doi: 10.1177/1534735416669803. Epub 2016 Oct 3.
Previously, we have shown that boehmenan, a natural product isolated from the dried stem of Caulis clematidis armandii, exhibits various biological activities. The current study investigated the effects of boehmenan on the growth of human epidermoid carcinoma A431 cells. Cell viability and 50% inhibiting concentration (IC) were assessed by CellTiter-Glo luminescent cell viability assay. Cell cycle arrest was measured by flow cytometry. Intracellular reactive oxygen species production and mitochondrial membrane potential (ΔΨ) collapse were analyzed by a fluorescence spectrophotometer. The activation of epidermal growth factor receptor signaling pathway was evaluated by Western blot. The results showed that boehmenan significantly inhibited the growth of A431 cells (IC = 1.6 µM) in a concentration- and time-dependent manner. This compound also blocked cell cycle progression at G2/M phase and modulated mitochondrial apoptosis-related proteins, as evidenced by upregulating p21, cleaved caspase-3, and cleaved poly (ADP-ribose) polymerase protein levels and by downregulating Bcl-2, pro-caspase-9 levels. In addition, boehmenan also markedly induced intracellular reactive oxygen species production and ΔΨ depolarization in a concentration-dependent manner. Furthermore, boehmenan-attenuated epidermal growth factor mediated the phosphorylation of signal transducer and activator of transcription 3 (STAT3), p70 ribosomal protein S6 kinase (p70S6)/S6 in a concentration-dependent manner. Taken together, our results suggest that boehmenan-mediated antiproliferative property in A431 cells was mediated partially by modulation of mitochondrial function and inhibition of STAT3 and p70S6 signal pathways.
此前,我们已经表明,从川木通干燥茎中分离得到的天然产物波密南具有多种生物活性。本研究调查了波密南对人表皮样癌A431细胞生长的影响。通过CellTiter-Glo发光细胞活力测定法评估细胞活力和50%抑制浓度(IC)。通过流式细胞术测量细胞周期停滞。用荧光分光光度计分析细胞内活性氧的产生和线粒体膜电位(ΔΨ)的崩溃。通过蛋白质印迹法评估表皮生长因子受体信号通路的激活。结果表明,波密南以浓度和时间依赖性方式显著抑制A431细胞的生长(IC = 1.6 μM)。该化合物还阻断了细胞周期在G2/M期的进程,并调节线粒体凋亡相关蛋白,这表现为上调p21、裂解的半胱天冬酶-3和裂解的聚(ADP-核糖)聚合酶蛋白水平,以及下调Bcl-2、前半胱天冬酶-9水平。此外,波密南还以浓度依赖性方式显著诱导细胞内活性氧的产生和ΔΨ去极化。此外,波密南减弱表皮生长因子介导的信号转导和转录激活因子3(STAT3)、p70核糖体蛋白S6激酶(p70S6)/S6的磷酸化,呈浓度依赖性。综上所述,我们的结果表明,波密南在A431细胞中介导的抗增殖特性部分是通过调节线粒体功能以及抑制STAT3和p70S6信号通路来实现的。