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番石榴叶水提物诱导前列腺癌细胞 LNCaP 凋亡的作用机制及信号通路研究。

Action mechanism and signal pathways of Psidium guajava L. aqueous extract in killing prostate cancer LNCaP cells.

机构信息

Department of Urology, Taipei Medical University-Shuang Ho Hospital, Taipei Medical University, Taipei, Taiwan.

出版信息

Nutr Cancer. 2010;62(2):260-70. doi: 10.1080/01635580903407130.

Abstract

Aqueous extract of Psidium guajava L. budding leaves (PE) has been shown to possess anti-prostate cancer activity in a cell line model. We examined whether its bioactivity could be conserved either in the presence or the absence of synthetic androgen R1881. In both cases, PE was shown to inhibit LNCaP cell proliferation and down-regulate expressions of androgen receptor (AR) and prostate specific antigen (PSA). The cytotoxicity of PE was shown by enhanced LDH release in LNCaP cells. The flow cytometry analysis revealed cell cycle arrests at G(0)/G(1) phase with huge amount of apoptotic LNCaP cells after treatment with PE for 48 h in a dose-responsive manner, which was also confirmed by TUNEL assay. From the results of decreased Bcl-2/Bax ratio, inactivation of phosphor-Akt, activation of phosphor-p38, phospho-Erk1/phospho-Erk2, the molecular action mechanism of PE to induce apoptosis in LNCaP cells was elucidated. Compatible with the in vitro study findings, treatment with PE (1.5 mg/mouse/day) significantly diminished both the PSA serum levels and tumor size in a xenograft mouse tumor model. Conclusively, PE is a promising anti-androgen-sensative prostate cancer agent.

摘要

番石榴叶芽水提物(PE)在细胞模型中表现出抗前列腺癌活性。我们研究了在存在或不存在合成雄激素 R1881 的情况下,其生物活性是否可以保持。在这两种情况下,PE 均能抑制 LNCaP 细胞增殖并下调雄激素受体(AR)和前列腺特异性抗原(PSA)的表达。PE 通过增强 LNCaP 细胞中的 LDH 释放来显示细胞毒性。流式细胞术分析显示,PE 处理 48 小时后,细胞周期停滞在 G0/G1 期,凋亡的 LNCaP 细胞数量巨大,呈剂量依赖性,TUNEL 检测也证实了这一点。从 Bcl-2/Bax 比值降低、磷酸化 Akt 失活、磷酸化 p38 激活、磷酸化 Erk1/磷酸化 Erk2 的结果来看,阐明了 PE 诱导 LNCaP 细胞凋亡的分子作用机制。与体外研究结果一致,PE(1.5mg/mouse/day)治疗显著降低了异种移植小鼠肿瘤模型中的 PSA 血清水平和肿瘤大小。总之,PE 是一种有前途的抗雄激素敏感前列腺癌药物。

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