Department of Pharmacology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.
School of Pharmaceutical Sciences, University of Science Malaysia, 11800 Minden, Penang, Malaysia.
PLoS One. 2015 Mar 31;10(3):e0121752. doi: 10.1371/journal.pone.0121752. eCollection 2015.
Quassinoids are a group of diterpenoids found in plants from the Simaroubaceae family. They are also the major bioactive compounds found in Eurycoma longifolia which is commonly used as traditional medicine in South East Asia to treat various ailments including sexual dysfunction and infertility. These uses are attributed to its ability to improve testosterone level in men. Chronic consumption of E. longifolia extracts has been reported to increase testosterone level in men and animal model but its effect on prostate growth remains unknown. Therefore, the present study investigates the effects of a standardized total quassinoids composition (SQ40) containing 40% of the total quassinoids found in E. longifolia on LNCaP human prostate cancer cell line. SQ40 inhibited LNCaP cell growth at IC50 value of 5.97 μg/mL while the IC50 on RWPE-1 human prostate normal cells was 59.26 μg/mL. SQ40 also inhibited 5α-dihydrotestosterone-stimulated growth in LNCaP cells dose-dependently. The inhibitory effect of SQ40 in anchorage-independent growth of LNCaP cells was also demonstrated using soft agar assay. SQ40 suppressed LNCaP cell growth via G0/G1 phase arrest which was accompanied by the down-regulation of CDK4, CDK2, Cyclin D1 and Cyclin D3 and up-regulation of p21Waf1/Cip1 protein levels. SQ40 at higher concentrations or longer treatment duration can cause G2M growth arrest leading to apoptotic cell death as demonstrated by the detection of poly(ADP-ribose) polymerase cleavage in LNCaP cells. Moreover, SQ40 also inhibited androgen receptor translocation to nucleus which is important for the transactivation of its target gene, prostate-specific antigen (PSA) and resulted in a significant reduction of PSA secretion after the treatment. In addition, intraperitoneal injection of 5 and 10 mg/kg of SQ40 also significantly suppressed the LNCaP tumor growth on mouse xenograft model. Results from the present study suggest that the standardized total quassinoids composition from E. longifolia promotes anti-prostate cancer activities in LNCaP human prostate cancer cells.
当归属植物中的苦味二萜类化合物。它们也是在常被用作东南亚传统药物的长柄铁心木(Eurycoma longifolia)中发现的主要生物活性化合物,用于治疗各种疾病,包括性功能障碍和不育。这些用途归因于它提高男性睾丸激素水平的能力。据报道,长期食用长柄铁心木提取物可提高男性和动物模型的睾丸激素水平,但它对前列腺生长的影响尚不清楚。因此,本研究调查了一种标准化的总苦味酸类化合物组合物(SQ40)对 LNCaP 人前列腺癌细胞系的影响,该组合物含有 40%的长柄铁心木中的总苦味酸类化合物。SQ40 在 5.97μg/mL 的 IC50 值下抑制 LNCaP 细胞生长,而在 RWPE-1 人前列腺正常细胞中的 IC50 值为 59.26μg/mL。SQ40 还可剂量依赖性地抑制 5α-二氢睾丸素刺激的 LNCaP 细胞生长。软琼脂试验也证明了 SQ40 对 LNCaP 细胞无锚定生长的抑制作用。SQ40 通过 G0/G1 期阻滞抑制 LNCaP 细胞生长,伴随着 CDK4、CDK2、Cyclin D1 和 Cyclin D3 的下调以及 p21Waf1/Cip1 蛋白水平的上调。SQ40 在较高浓度或较长的治疗时间下可导致 G2M 生长阻滞,导致凋亡细胞死亡,如 LNCaP 细胞中多聚(ADP-核糖)聚合酶裂解的检测所示。此外,SQ40 还抑制雄激素受体向核内易位,这对于其靶基因前列腺特异性抗原(PSA)的转录激活很重要,导致治疗后 PSA 分泌显著减少。此外,腹腔注射 5 和 10mg/kg 的 SQ40 也显著抑制了小鼠异种移植模型中 LNCaP 肿瘤的生长。本研究结果表明,长柄铁心木的标准化总苦味酸类化合物组合物在 LNCaP 人前列腺癌细胞中具有促进抗前列腺癌活性。