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BZL101 是一种来自黄芩植物的植物化学提取物,通过依赖于癌细胞表型的不同机制,破坏人类乳腺癌和前列腺癌细胞的增殖。

BZL101, a phytochemical extract from the Scutellaria barbata plant, disrupts proliferation of human breast and prostate cancer cells through distinct mechanisms dependent on the cancer cell phenotype.

机构信息

Department of Molecular and Cell Biology, University of California at Berkeley, USA.

出版信息

Cancer Biol Ther. 2010 Aug 15;10(4):397-405. doi: 10.4161/cbt.10.4.12424. Epub 2010 Aug 20.

Abstract

BZL101 is an aqueous extract from the Scutellaria barbata plant shown to have anticancer properties in a variety of human cancers. In order to determine its efficacy on human reproductive cancers, we assessed the responses of two human breast cancer cell lines, estrogen sensitive MCF7 and estrogen insensitive MDA-MB-231, and of two human prostate cancer cell lines, androgen sensitive LNCaP and androgen insensitive PC3 which are human cell lines that represent early and late stage reproductive cancers. BZL101 inhibited reproductive cancer growth in all cell lines by regulating expression levels of key cell cycle components that differ with respect to the cancer cell phenotypes. In early stage estrogen sensitive MCF7 cells, BZL101 induced a G₁ cell cycle arrest and ablated expression of key G₁ cell cycle regulators Cyclin D1, CDK2 and CDK4, as well as growth factor stimulatory pathways and estrogen receptor-α expression. Transfection of luciferase reporter plasmids revealed that the loss of CDK2, CDK4 and estrogen receptor-α transcript expression resulted from the BZL-dependent ablation of promoter activities. BZL101 growth arrests early stage androgen sensitive LNCaP cells in the G₂/M phase with corresponding decreases in Cyclin B1, CDK1 and androgen receptor expression. In late stage hormone insensitive breast (MDA-MB-231) and prostate (PC3) cancer cells, BZL101 induced an S phase arrest with corresponding ablations in Cyclin A2 and CDK2 expression. Our results demonstrate that BZL101 exerts phenotype specific anti-proliferative gene expression responses in human breast and prostate cancer cells, which will be valuable in the potential development of BZL-based therapeutic strategies for human reproductive cancers.

摘要

BZL101 是一种从黄芩植物中提取的水性提取物,已被证明在多种人类癌症中具有抗癌特性。为了确定其对人类生殖系统癌症的疗效,我们评估了两种人乳腺癌细胞系(雌激素敏感 MCF7 和雌激素不敏感 MDA-MB-231)以及两种人前列腺癌细胞系(雄激素敏感 LNCaP 和雄激素不敏感 PC3)的反应,这些细胞系代表了生殖系统癌症的早期和晚期阶段。BZL101 通过调节关键细胞周期成分的表达水平来抑制所有细胞系的生殖系统癌症生长,这些细胞周期成分的表达水平因癌细胞表型而异。在早期雌激素敏感 MCF7 细胞中,BZL101 诱导 G₁ 细胞周期停滞并消除关键 G₁ 细胞周期调节剂细胞周期蛋白 D1、CDK2 和 CDK4 的表达,以及生长因子刺激途径和雌激素受体-α的表达。荧光素酶报告质粒的转染表明,CDK2、CDK4 和雌激素受体-α 转录本表达的丧失是由于 BZL 依赖性启动子活性的消融。BZL101 使早期雄激素敏感 LNCaP 细胞在 G₂/M 期停滞,相应的 Cyclin B1、CDK1 和雄激素受体表达减少。在晚期激素不敏感的乳腺癌(MDA-MB-231)和前列腺癌(PC3)细胞中,BZL101 诱导 S 期停滞,相应的 Cyclin A2 和 CDK2 表达减少。我们的结果表明,BZL101 在人乳腺癌和前列腺癌细胞中发挥表型特异性的抗增殖基因表达反应,这将对基于 BZL 的治疗策略的潜在发展具有重要价值。

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