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Expression of prostate stem cell antigen is downregulated during flavonoid-induced cytotoxicity in prostate cancer cells.在黄酮类化合物诱导前列腺癌细胞产生细胞毒性的过程中,前列腺干细胞抗原的表达下调。
Exp Ther Med. 2017 Aug;14(2):1795-1801. doi: 10.3892/etm.2017.4638. Epub 2017 Jun 21.
2
Dietary Flavonoids Luteolin and Quercetin Suppressed Cancer Stem Cell Properties and Metastatic Potential of Isolated Prostate Cancer Cells.膳食类黄酮木犀草素和槲皮素可抑制分离出的前列腺癌细胞的癌症干细胞特性和转移潜能。
Anticancer Res. 2016 Dec;36(12):6367-6380. doi: 10.21873/anticanres.11234.
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Knockdown of PSCA induces EMT and decreases metastatic potentials of the human prostate cancer DU145 cells.敲低前列腺干细胞抗原(PSCA)可诱导人前列腺癌DU145细胞发生上皮-间质转化(EMT)并降低其转移潜能。
Cancer Cell Int. 2016 Mar 15;16:20. doi: 10.1186/s12935-016-0295-4. eCollection 2016.
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Detrimental effect of cancer preventive phytochemicals silymarin, genistein and epigallocatechin 3-gallate on epigenetic events in human prostate carcinoma DU145 cells.癌症预防植物化学物质水飞蓟素、染料木黄酮和表没食子儿茶素3-没食子酸酯对人前列腺癌DU145细胞表观遗传事件的有害影响。
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Flavonoid Calycopterin Induces Apoptosis in Human Prostate Cancer Cells .黄酮类化合物毛鱼藤酮诱导人前列腺癌细胞凋亡。
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本文引用的文献

1
Dietary Flavonoids Luteolin and Quercetin Suppressed Cancer Stem Cell Properties and Metastatic Potential of Isolated Prostate Cancer Cells.膳食类黄酮木犀草素和槲皮素可抑制分离出的前列腺癌细胞的癌症干细胞特性和转移潜能。
Anticancer Res. 2016 Dec;36(12):6367-6380. doi: 10.21873/anticanres.11234.
2
Knockdown of PSCA induces EMT and decreases metastatic potentials of the human prostate cancer DU145 cells.敲低前列腺干细胞抗原(PSCA)可诱导人前列腺癌DU145细胞发生上皮-间质转化(EMT)并降低其转移潜能。
Cancer Cell Int. 2016 Mar 15;16:20. doi: 10.1186/s12935-016-0295-4. eCollection 2016.
3
Prostate cancer relevant antigens and enzymes for targeted drug delivery.用于靶向给药的前列腺癌相关抗原和酶
J Control Release. 2014 Aug 10;187:118-32. doi: 10.1016/j.jconrel.2014.05.035. Epub 2014 May 27.
4
Antiproliferative and apoptotic effects of a specific antiprostate stem cell single chain antibody on human prostate cancer cells.抗前列腺干细胞单链抗体对人前列腺癌细胞的增殖抑制和凋亡作用。
J Oncol. 2013;2013:839831. doi: 10.1155/2013/839831. Epub 2013 Dec 10.
5
Flavonoids as prospective compounds for anti-cancer therapy.类黄酮作为抗癌治疗的有前景的化合物。
Int J Biochem Cell Biol. 2013 Dec;45(12):2821-31. doi: 10.1016/j.biocel.2013.10.004. Epub 2013 Oct 12.
6
Oral administration of naturally occurring chitosan-based nanoformulated green tea polyphenol EGCG effectively inhibits prostate cancer cell growth in a xenograft model.口服天然壳聚糖基纳米配方绿茶多酚 EGCG 能有效抑制异种移植模型中的前列腺癌细胞生长。
Carcinogenesis. 2014 Feb;35(2):415-23. doi: 10.1093/carcin/bgt321. Epub 2013 Sep 26.
7
Genistein inhibits prostate cancer cell growth by targeting miR-34a and oncogenic HOTAIR.金雀异黄素通过靶向 miR-34a 和致癌基因 HOTAIR 抑制前列腺癌细胞生长。
PLoS One. 2013 Aug 1;8(8):e70372. doi: 10.1371/journal.pone.0070372. Print 2013.
8
Genistein induces G2/M cell cycle arrest and apoptosis via ATM/p53-dependent pathway in human colon cancer cells.染料木黄酮通过 ATM/p53 依赖性途径诱导人结肠癌细胞 G2/M 细胞周期阻滞和凋亡。
Int J Oncol. 2013 Jul;43(1):289-96. doi: 10.3892/ijo.2013.1946. Epub 2013 May 17.
9
Quercetin synergizes with 2-methoxyestradiol inhibiting cell growth and inducing apoptosis in human prostate cancer cells.槲皮素与 2-甲氧基雌二醇协同抑制人前列腺癌细胞的生长并诱导其凋亡。
Oncol Rep. 2013 Jul;30(1):357-63. doi: 10.3892/or.2013.2469. Epub 2013 May 15.
10
The roles of endoplasmic reticulum stress and mitochondrial apoptotic signaling pathway in quercetin-mediated cell death of human prostate cancer PC-3 cells.内质网应激和线粒体凋亡信号通路在槲皮素介导的人前列腺癌 PC-3 细胞死亡中的作用。
Environ Toxicol. 2014 Apr;29(4):428-39. doi: 10.1002/tox.21769. Epub 2012 Mar 20.

在黄酮类化合物诱导前列腺癌细胞产生细胞毒性的过程中,前列腺干细胞抗原的表达下调。

Expression of prostate stem cell antigen is downregulated during flavonoid-induced cytotoxicity in prostate cancer cells.

作者信息

Zhang Qiang, Cheng Guangdong, Qiu Hongbin, Wang Yuexin, Wang Jingtao, Xu Hui, Zhang Tao, Liu Lixin, Tao Ye, Ren Zhongjuan

机构信息

Department of Preventive Medicine, School of Public Health, Jiamusi University, Jiamusi, Heilongjiang 154007, P.R. China.

Department of Animal Science, College of Life Science, Jiamusi University, Jiamusi, Heilongjiang 154007, P.R. China.

出版信息

Exp Ther Med. 2017 Aug;14(2):1795-1801. doi: 10.3892/etm.2017.4638. Epub 2017 Jun 21.

DOI:10.3892/etm.2017.4638
PMID:28810652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5526134/
Abstract

Prostate stem cell antigen (PSCA) is expressed in the majority of prostate cancer cases and may be a potential therapeutic target in the treatment of prostate cancer. The present study evaluated the cytotoxicity of three flavonoids (genistein, luteolin and quercetin) towards DU145 prostate cancer cells, and investigated the effect of these flavonoids on PSCA expression. The results demonstrated that genistein, luteolin and quercetin inhibited the growth of DU145 cells in a dose-dependent manner (P<0.05) and induced morphological changes characteristic of apoptosis in DU145 cells. Flow cytometry analysis also indicated that the flavonoids induced S phase cycle arrest in DU145 cells. Notably, it was observed that expression of PSCA was inhibited at the mRNA (P<0.05) and protein levels in DU145 cells following flavonoid treatment compared with the control. These results suggest that flavonoids may be potential therapeutic agents in the treatment and prevention of prostate cancer.

摘要

前列腺干细胞抗原(PSCA)在大多数前列腺癌病例中表达,可能是前列腺癌治疗中的一个潜在治疗靶点。本研究评估了三种黄酮类化合物(染料木黄酮、木犀草素和槲皮素)对DU145前列腺癌细胞的细胞毒性,并研究了这些黄酮类化合物对PSCA表达的影响。结果表明,染料木黄酮、木犀草素和槲皮素以剂量依赖性方式抑制DU145细胞的生长(P<0.05),并诱导DU145细胞出现凋亡特征性的形态变化。流式细胞术分析还表明,这些黄酮类化合物诱导DU145细胞S期周期阻滞。值得注意的是,观察到与对照组相比,黄酮类化合物处理后DU145细胞中PSCA的mRNA(P<0.05)和蛋白质水平表达受到抑制。这些结果表明,黄酮类化合物可能是治疗和预防前列腺癌的潜在治疗药物。