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Cytotoxic and chemosensitization effects of Scutellarin from traditional Chinese herb Scutellaria altissima L. in human prostate cancer cells

机译:中草药黄cut中黄prostate苷对人前列腺癌细胞的细胞毒和化学增敏作用

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摘要

Scutellaria altissima L. is a common traditional Chinese medicine used to treat inflammation in some countries. Scutellarin, an active major flavone glycoside isolated from the traditional Chinese medicine Scutellaria altissima L., has been shown to offer various beneficial biochemical effects on cerebrovascular diseases and inflammation. However, the antiproliferative effects of Scutellarin in prostate cancer and the underlying mechanism are not fully elucidated. In the present study, we aimed to ascertain whether Scutellarin inhibits cancer cell growth and to further explore the molecular mechanism. Scutellarin enhanced the sensitivity of prostate cancer cells to cisplatin. MTT assays revealed that cell viability was significantly decreased in the prostate cancer cells treated with Scutellarin. Flow cytometric analysis indicated that Scutellarin suppressed cell proliferation by promoting G2/M arrest and inducing apoptosis. We employed western blotting to delineate the underlying mechanisms involved in the G2/M arrest and apoptosis. Comet assay and γH2AX immunocytochemistry were used to detect levels of DNA damage in PC3 cells exposed to Scutellarin and/or cisplatin. Our data revealed that Scutellarin significantly induced prostate cancer cell apoptosis by activating the caspase cascade. An increase in the Bax/Bcl-2 ratio, depolarization of mitochondrial membrane potential and cell cycle arrest at G2/M phase were accompanied by the apoptosis induction. Additionally, Scutellarin altered the protein expression of cell cycle and apoptosis regulatory genes by downregulating Cdc2, cyclin B1 and Bcl-2 and upregulating caspase-3, caspase-9 and Bax in prostate cancer cells. Furthermore, Scutellarin sensitized PC3 cells to cisplastin treatment in a dose-dependent manner. Taken together, our data confirmed the cytotoxicity of Scutellarin against prostate cancer PC3 cells and provide new findings in regards to Scutellarin sensitizing prostate cancer cells to chemotherapy. Our findings suggest that Scutellarin has potential to be used as a novel antineoplastic therapeutic candidate for prostate cancer patients.
机译:黄cut是在一些国家中用于治疗炎症的常见中药。黄cut苷是一种从传统中药黄cut中分离出的活性主要黄酮苷,已被证明对脑血管疾病和炎症具有多种有益的生化作用。然而,黄cut苷在前列腺癌中的抗增殖作用及其潜在机制尚未完全阐明。在本研究中,我们旨在确定黄cut苷是否抑制癌细胞的生长并进一步探索其分子机制。黄cut苷增强了前列腺癌细胞对顺铂的敏感性。 MTT分析显示,在用黄cut苷处理过的前列腺癌细胞中,细胞活力显着降低。流式细胞仪分析表明,黄cut苷可通过促进G2 / M阻滞并诱导细胞凋亡来抑制细胞增殖。我们采用蛋白质印迹来描述参与G2 / M阻滞和凋亡的潜在机制。使用彗星试验和γH2AX免疫细胞化学来检测暴露于黄cut素和/或顺铂的PC3细胞中DNA损伤的水平。我们的数据显示,黄cut苷通过激活半胱天冬酶级联反应显着诱导前列腺癌细胞凋亡。 Bax / Bcl-2比的增加,线粒体膜电位的去极化和G2 / M期的细胞周期停滞都伴随着凋亡的诱导。此外,黄cut苷通过下调前列腺癌细胞中的Cdc2,细胞周期蛋白B1和Bcl-2并上调caspase-3,caspase-9和Bax来改变细胞周期和凋亡调控基因的蛋白表达。此外,黄cut苷以剂量依赖的方式使PC3细胞对顺铂进行治疗。两者合计,我们的数据证实了黄cut素对前列腺癌PC3细胞的细胞毒性,并在黄cut素使前列腺癌细胞对化学疗法敏感的方面提供了新的发现。我们的发现表明,黄S素具有用作前列腺癌患者的新型抗肿瘤治疗候选物的潜力。

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