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Cell Biochem Funct. 2021 Aug;39(6):813-820. doi: 10.1002/cbf.3654. Epub 2021 Jun 14.
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Epigallocatechin-3-gallate Enhances the Efficacy of MicroRNA-34a Mimic and MicroRNA-93 Inhibitor Co-transfection in Prostate Cancer Cell Line.没食子酸表没食子儿茶素酯增强 miRNA-34a 模拟物和 miRNA-93 抑制剂共转染在前列腺癌细胞系中的疗效。
Iran J Allergy Asthma Immunol. 2020 Dec 19;19(6):612-623. doi: 10.18502/ijaai.v19i6.4930.
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Evaluating the in vitro therapeutic effects of human amniotic mesenchymal stromal cells on MiaPaca2 pancreatic cancer cells using 2D and 3D cell culture model.评估人羊膜间充质基质细胞在二维和三维细胞培养模型中对 MiaPaca2 胰腺癌细胞的体外治疗效果。
Tissue Cell. 2021 Feb;68:101479. doi: 10.1016/j.tice.2020.101479. Epub 2020 Dec 23.
4
Involvement of MicroRNA-296 in the Inhibitory Effect of Epigallocatechin Gallate against the Migratory Properties of Anoikis-Resistant Nasopharyngeal Carcinoma Cells.微小RNA-296参与表没食子儿没食子酸酯对耐失巢凋亡鼻咽癌细迁移特性的抑制作用
Cancers (Basel). 2020 Apr 15;12(4):973. doi: 10.3390/cancers12040973.
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Enzalutamide with Standard First-Line Therapy in Metastatic Prostate Cancer.恩扎卢胺联合标准一线治疗转移性前列腺癌。
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Apalutamide for Metastatic, Castration-Sensitive Prostate Cancer.阿帕鲁胺治疗转移性去势敏感性前列腺癌。
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Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.全球癌症统计数据 2018:GLOBOCAN 对全球 185 个国家/地区 36 种癌症的发病率和死亡率的估计。
CA Cancer J Clin. 2018 Nov;68(6):394-424. doi: 10.3322/caac.21492. Epub 2018 Sep 12.
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The Role and Mechanism of Epithelial-to-Mesenchymal Transition in Prostate Cancer Progression.上皮-间质转化在前列腺癌进展中的作用和机制。
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绿茶提取物通过上调 miR-195 的表达和抑制上皮间质转化对 PC3 前列腺癌细胞的疗效。

Efficacy of green tea extract on PC3 prostate cancer cells through upregulation of miR-195 expression and suppression of epithelial to mesenchymal transition.

机构信息

Department of Biology, Faculty of Science, University of Guilan, Rasht 4193833697, Iran.

Department of Microbiology, North Tehran Branch, Islamic Azad University, Tehran 1651153511, Iran.

出版信息

J Tradit Chin Med. 2022 Oct;42(5):681-686. doi: 10.19852/j.cnki.jtcm.2022.05.002.

DOI:10.19852/j.cnki.jtcm.2022.05.002
PMID:36083473
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9924716/
Abstract

OBJECTIVE

To evaluate anticancer efficacy of green tea extract (GTE) on PC3 prostate cancer cells.

METHODS

By using quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot methods, the expression of miR-195 and the epithelial to mesenchymal transition (EMT) markers such as E-cadherin and vimentin was analyzed.

RESULTS

Based on the results of 2D and 3D cell culture models, the inhibition of EMT and up regulation of miR-195 expression were detected.

CONCLUSIONS

Our findings will be helpful to design anti-tumor regimens with natural product original, and more studies will be required to identify the related mechanisms involving anticancer activities of green tea miRNAs.

摘要

目的

评估绿茶提取物(GTE)对 PC3 前列腺癌细胞的抗癌功效。

方法

采用实时定量聚合酶链反应(qRT-PCR)和 Western blot 方法分析 miR-195 的表达和上皮间质转化(EMT)标志物如 E-钙黏蛋白和波形蛋白的表达。

结果

基于 2D 和 3D 细胞培养模型的结果,检测到 EMT 的抑制和 miR-195 表达的上调。

结论

我们的研究结果将有助于设计具有天然产物原始特性的抗肿瘤方案,还需要更多的研究来确定涉及绿茶 miRNA 抗癌活性的相关机制。