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啤酒花中天然化合物黄腐酚处理后,肿瘤坏死因子相关凋亡诱导配体诱导前列腺癌细胞凋亡

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.

作者信息

Kłósek Małgorzata, Mertas Anna, Król Wojciech, Jaworska Dagmara, Szymszal Jan, Szliszka Ewelina

机构信息

Chair and Department of Microbiology and Immunology, School of Medicine with Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, Jordana 19, 41-808 Zabrze, Poland.

Department of Production Engineering, Faculty of Materials Engineering and Metallurgy, Silesian University of Technology, Krasińskiego 8b, 40-019 Katowice, Poland.

出版信息

Int J Mol Sci. 2016 Jun 22;17(6):837. doi: 10.3390/ijms17060837.

Abstract

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.

摘要

肿瘤坏死因子相关凋亡诱导配体(TRAIL)是一种内源性配体,在免疫监视和抗肿瘤免疫中发挥作用。它能够选择性地杀死肿瘤细胞,而对正常细胞无毒性。我们测试了在啤酒花中发现的一种异戊烯基化查耳酮——黄腐酚,与TRAIL联合作用于雄激素敏感的人前列腺腺癌细胞(LNCaP)时的凋亡和细胞毒性活性。通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐还原法(MTT)和乳酸脱氢酶法(LDH)测定细胞毒性。使用流式细胞术检测死亡受体(DR4/TRAIL-R1和DR5/TRAIL-R2)的表达及凋亡情况。通过荧光显微镜使用DePsipher试剂检测线粒体膜电位(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了半胱天冬酶-3、-8、-9、Bid,并增加了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,而死亡受体的表达没有变化。这些发现表明,黄腐酚因其使癌细胞对TRAIL介导的凋亡敏感,是一种在前列腺癌化学预防中具有潜在用途的化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1b0/4926371/521833bec22a/ijms-17-00837-g001.jpg

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