Department of Pharmacology, School of Pharmaceutical Sciences, Jilin University, 1266 Fujin Rd., Changchun, Jilin Province 130021, PR China.
Bioorg Med Chem Lett. 2013 Jun 15;23(12):3631-4. doi: 10.1016/j.bmcl.2013.04.007. Epub 2013 Apr 11.
Juglone is a natural compound which has been isolated from Juglans mandshurica Maxim. Recent studies have shown that juglone had various pharmacological effects such as anti-viral, anti-bacterial and anti-cancer. However, its anti-cancer activity on human prostate cancer LNCaP cell has not been examined. Thus, the current study was designed to elucidate the molecular mechanism of apoptosis induced by juglone in androgen-sensitive prostate cancer LNCaP cells. MTT assay was performed to examine the anti-proliferative effect of juglone. Occurrence of apoptosis was detected by Hoechst 33342 staining and flow cytometry in LNCaP cells treated with juglone for 24h. The result shown that juglone inhibited the growth of LNCaP cells in a dose-dependent manner. Morphological changes of apoptotic body formation after juglone treatment were observed by Hoechst 33342 staining. This apoptotic induction was associated with loss of mitochondrial membrane potential, and caspase-3, -9 activation. Moreover, we found that juglone significantly inhibited the expression levels of androgen receptor (AR) and prostate-specific antigen (PSA) in a dose-dependent manner, as well as abrogated up-regulation of AR and PSA genes with and/or without dihydrotestosterone (DHT). Take together, our results demonstrated that juglone might induce the apoptosis in LNCaP cell via down-regulation of AR expression. Therefore, our results indicated that juglone may be a potential candidate of drug for androgen-sensitive prostate cancer.
胡桃醌是一种从胡桃科植物核桃中分离得到的天然化合物。最近的研究表明,胡桃醌具有多种药理作用,如抗病毒、抗菌和抗癌作用。然而,其对人前列腺癌 LNCaP 细胞的抗癌活性尚未得到检验。因此,本研究旨在阐明胡桃醌诱导雄激素敏感前列腺癌 LNCaP 细胞凋亡的分子机制。MTT 法检测胡桃醌对 LNCaP 细胞的增殖抑制作用。用 Hoechst 33342 染色和流式细胞术检测 LNCaP 细胞在胡桃醌作用 24 小时后的凋亡发生情况。结果表明,胡桃醌呈剂量依赖性抑制 LNCaP 细胞的生长。Hoechst 33342 染色观察到胡桃醌处理后凋亡小体形成的形态学变化。这种凋亡诱导与线粒体膜电位丧失和 caspase-3、-9 激活有关。此外,我们发现胡桃醌呈剂量依赖性显著抑制雄激素受体 (AR) 和前列腺特异性抗原 (PSA) 的表达水平,并阻断了雄激素 (DHT) 加或不加 DHT 对 AR 和 PSA 基因的上调。综上所述,我们的研究结果表明,胡桃醌可能通过下调 AR 表达诱导 LNCaP 细胞凋亡。因此,我们的研究结果表明,胡桃醌可能是一种治疗雄激素敏感前列腺癌的潜在候选药物。