School of Biomedical Sciences, Faculty of Health Sciences, Curtin University, Kent Street, Bentley, Western Australia, Australia.
J Biosci. 2012 Mar;37(1):73-84. doi: 10.1007/s12038-011-9170-6.
Phenoxodiol is an isoflavone derivative that has been shown to elicit cytotoxic effects against a broad range of human cancers. We examined the effect of phenoxodiol on cell death pathways on the prostate cell lines LNCaP, DU145 and PC3, representative of different stages of prostate cancer, and its effects on cell death pathways in these cell lines. Cell proliferation assays demonstrated a significant reduction in the rate of cell proliferation after 48 h exposure to phenoxodiol (10 and 30 μM). FACS analysis and 3'-end labelling indicated that all three prostate cancer cell lines underwent substantial levels of cell death 48 h after treatment. Mitochondrial membrane depolarization, indicative of early-stage cell death signalling, using JC-1 detection, was also apparent in all cell lines after exposure to phenoxodiol in the absence of caspase-3 activation. Caspase inhibition assays indicated that phenoxodiol operates through a caspase-independent cell death pathway. These data demonstrate that phenoxodiol elicits anti-cancer effects in prostate cancer cell lines representative of early and later stages of development through an as-yet-unknown cell death mechanism. These data warrant the further investigation of phenoxodiol as a potential treatment for prostate cancer.
苯氧二醇是一种异黄酮衍生物,已被证明对广泛的人类癌症具有细胞毒性作用。我们研究了苯氧二醇对不同前列腺癌阶段的前列腺细胞系 LNCaP、DU145 和 PC3 细胞死亡途径的影响及其对这些细胞系中细胞死亡途径的影响。细胞增殖测定表明,苯氧二醇(10 和 30 μM)暴露 48 小时后,细胞增殖率显著降低。FACS 分析和 3'-末端标记表明,所有三种前列腺癌细胞系在治疗 48 小时后都经历了大量的细胞死亡。在用 JC-1 检测时,线粒体膜去极化,表明早期细胞死亡信号,在没有 caspase-3 激活的情况下,苯氧二醇暴露后,所有细胞系中也都出现了这种现象。半胱氨酸蛋白酶抑制测定表明,苯氧二醇通过一种半胱天冬酶非依赖性细胞死亡途径发挥作用。这些数据表明,苯氧二醇通过一种未知的细胞死亡机制,在代表早期和晚期发展阶段的前列腺癌细胞系中引发抗癌作用。这些数据证明了苯氧二醇作为前列腺癌潜在治疗方法的进一步研究。