首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand-Induced Apoptosis in Prostate Cancer Cells after Treatment with Xanthohumol—A Natural Compound Present in Humulus lupulus L.
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Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand-Induced Apoptosis in Prostate Cancer Cells after Treatment with Xanthohumol—A Natural Compound Present in Humulus lupulus L.

机译:黄腐酚(一种存在于Hum草中的天然化合物)治疗后肿瘤坏死因子相关的凋亡诱导配体诱导的前列腺癌细胞凋亡。

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摘要

TRAIL (tumor necrosis factor-related apoptosis-inducing ligand) is an endogenous ligand, which plays role in immune surveillance and anti-tumor immunity. It has ability to selectively kill tumor cells showing no toxicity to normal cells. We tested the apoptotic and cytotoxic activities of xanthohumol, a prenylated chalcone found in Humulus lupulus on androgen-sensitive human prostate adenocarcinoma cells (LNCaP) in combination with TRAIL. Cytotoxicity was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide tetrazolium reduction assay (MTT) and lactate dehydrogenase assay (LDH). The expression of death receptors (DR4/TRAIL-R1 and DR5/TRAIL-R2) and apoptosis were detected using flow cytometry. We examined mitochondrial membrane potential (ΔΨm) by DePsipher reagent using fluorescence microscopy. The intracellular expression of proteins was evaluated by Western blotting. Our study showed that xanthohumol enhanced cytotoxic and apoptotic effects of TRAIL. The tested compounds activated caspases-3, -8, -9, Bid, and increased the expression of Bax. They also decreased expression of Bcl-xL and decreased mitochondrial membrane potential, while the expression of death receptors was not changed. The findings suggest that xanthohumol is a compound of potential use in chemoprevention of prostate cancer due to its sensitization of cancer cells to TRAIL-mediated apoptosis.
机译:TRAIL(与肿瘤坏死因子相关的凋亡诱导配体)是一种内源性配体,在免疫监视和抗肿瘤免疫中发挥作用。它具有选择性杀伤对正常细胞无毒性的肿瘤细胞的能力。我们测试了黄腐酚(一种在Hum草中发现的烯丙基化查耳酮)对雄激素敏感的人前列腺腺癌细胞(LNCaP)与TRAIL组合的凋亡和细胞毒活性。通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四溴化四唑还原测定法(MTT)和乳酸脱氢酶测定法(LDH)测定细胞毒性。流式细胞仪检测死亡受体(DR4 / TRAIL-R1和DR5 / TRAIL-R2)的表达和凋亡。我们使用荧光显微镜通过DePsipher试剂检查了线粒体膜电位(ΔΨm)。通过蛋白质印迹法评估蛋白质的细胞内表达。我们的研究表明,黄腐酚增强了TRAIL的细胞毒性和凋亡作用。所测试的化合物激活caspases-3,-8,-9,Bid并增加Bax的表达。它们还降低了Bcl-xL的表达并降低了线粒体膜电位,而死亡受体的表达未改变。研究结果表明,由于黄嘌呤酚使癌细胞对TRAIL介导的细胞凋亡敏感,因此它是化学预防前列腺癌的潜在化合物。

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