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Evaluation of the hepatoprotective effect of Yigan mingmu oral liquid against acute alcohol-induced liver injury in rats.评价益肝明目口服液对大鼠急性酒精性肝损伤的保护作用。
BMC Complement Med Ther. 2020 Feb 5;20(1):32. doi: 10.1186/s12906-020-2817-9.
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Ovatodiolide Suppresses Oral Cancer Malignancy by Down-Regulating Exosomal Mir-21/STAT3/β-Catenin Cargo and Preventing Oncogenic Transformation of Normal Gingival Fibroblasts.卵叶二萜内酯通过下调外泌体Mir-21/STAT3/β-连环蛋白货物并防止正常牙龈成纤维细胞的致癌转化来抑制口腔癌恶性肿瘤。
Cancers (Basel). 2019 Dec 24;12(1):56. doi: 10.3390/cancers12010056.
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HOXD-AS1 confers cisplatin resistance in gastric cancer through epigenetically silencing PDCD4 via recruiting EZH2.HOXD-AS1 通过招募 EZH2 表观遗传沉默 PDCD4 赋予胃癌顺铂耐药性。
Open Biol. 2019 Sep 27;9(9):190068. doi: 10.1098/rsob.190068. Epub 2019 Sep 25.
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STAT3 inhibitor WP1066 attenuates miRNA-21 to suppress human oral squamous cell carcinoma growth in vitro and in vivo.信号转导和转录激活因子3(STAT3)抑制剂WP1066可下调微小RNA-21(miRNA-21),从而在体外和体内抑制人口腔鳞状细胞癌的生长。
Oncol Rep. 2014 May;31(5):2173-80. doi: 10.3892/or.2014.3114. Epub 2014 Mar 27.
6
MiR-21 modulates chemosensitivity of tongue squamous cell carcinoma cells to cisplatin by targeting PDCD4.微小RNA-21通过靶向程序性细胞死亡蛋白4调节舌鳞状细胞癌细胞对顺铂的化疗敏感性。
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7
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Set9, NF-κB, and microRNA-21 mediate berberine-induced apoptosis of human multiple myeloma cells.Set9、NF-κB 和 microRNA-21 介导小檗碱诱导的人多发性骨髓瘤细胞凋亡。
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芪兰制剂通过下调人舌鳞状细胞癌细胞中 microRNA-21 的表达抑制增殖并诱导凋亡。

Qilan preparation inhibits proliferation and induces apoptosis by down-regulating microRNA-21 in human Tca8113 tongue squamous cell carcinoma cells.

机构信息

Department of Oral Mucosal Diseases, Affiliated Stomatological Hospital of Fujian Medical University, Fuzhou 350000, China.

School and Hospital of Stomatology, Fujian Medical University, Fuzhou 350000, China.

出版信息

J Tradit Chin Med. 2022 Oct;42(5):693-700. doi: 10.19852/j.cnki.jtcm.2022.05.003.

DOI:10.19852/j.cnki.jtcm.2022.05.003
PMID:36083475
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9924750/
Abstract

OBJECTIVE

The aim of this study was to examine the antitumor effects of Qilan preparation on oral squamous cell carcinoma (OSCC) and to investigate its underlying mechanisms of action.

METHODS

Cell proliferation, cell cycle distribution and apoptosis were examined using cell counting kit-8 (CCK8) and flow cytometry (FCM). The expression of PTEN and PDCD4 were determined by western blot. Changes in miR-21 levels were quantified using TaqMan stem-loop real-time PCR. After miR-21 was transiently transfected into Tca8113 cells using Lipofectamine®3000, cell proliferation, apoptosis and miR-21 and PDCD4 expression levels were measured.

RESULTS

Qilan preparation inhibited Tca8113 cell growth in a dose- and time-dependent manner by inducing apoptosis and cell cycle arrest in S-phase, decreasing miR-21 levels and increasing PTEN and PDCD4 expression. MiR-21 overexpression reversed the Qilan preparation-induced suppression of cell proliferation and induction of apoptosis while also blocking the increase in PDCD4.

CONCLUSIONS

Our study revealed, for the first time, the ability of Qilan preparation to suppress TSCC cell growth and elucidated that Qilan preparation elicits its anti-cancer actions either the miR-21/PDCD4 or PTEN pathway.

摘要

目的

本研究旨在探讨芪兰制剂对口腔鳞状细胞癌(OSCC)的抗肿瘤作用,并探讨其作用机制。

方法

采用细胞计数试剂盒-8(CCK8)和流式细胞术(FCM)检测细胞增殖、细胞周期分布和细胞凋亡。采用 Western blot 检测 PTEN 和 PDCD4 的表达。采用 TaqMan 茎环实时 PCR 定量检测 miR-21 水平的变化。用 Lipofectamine®3000 将 miR-21 瞬时转染 Tca8113 细胞后,检测细胞增殖、细胞凋亡以及 miR-21 和 PDCD4 的表达水平。

结果

芪兰制剂以剂量和时间依赖的方式抑制 Tca8113 细胞生长,通过诱导细胞凋亡和 S 期细胞周期阻滞,降低 miR-21 水平,增加 PTEN 和 PDCD4 的表达。miR-21 的过表达逆转了芪兰制剂对细胞增殖的抑制和诱导的凋亡,同时阻断了 PDCD4 的增加。

结论

本研究首次揭示了芪兰制剂抑制 TSCC 细胞生长的能力,并阐明芪兰制剂通过 miR-21/PDCD4 或 PTEN 通路发挥其抗癌作用。