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丹参酮IIA通过下调P-糖蛋白和LC3-II增强5-氟尿嘧啶在体内对Colo205结肠癌细胞的疗效。

Tanshinone IIA potentiates the efficacy of 5-FU in Colo205 colon cancer cells in vivo through downregulation of P-gp and LC3-II.

作者信息

Su Chin-Cheng

机构信息

Department of Surgery, Changhua Christian Hospital, Changhua, Changhua 500-06; Mingdao University, Pee-Tow, Changhua 52345; School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung 40402, Taiwan, R.O.C.

出版信息

Exp Ther Med. 2012 Mar;3(3):555-559. doi: 10.3892/etm.2011.441. Epub 2011 Dec 28.

Abstract

Traditional Chinese herbal medicines are widely accepted as an option for the treatment of colorectal cancers. Danshen (Salviae miltiorrhizae Radix) is widely prescribed in traditional Chinese medicine for cardiovascular diseases. Tanshinone IIA (Tan-IIA) is extracted from Danshen. Our previous studies have shown that Tan-IIA induces apoptosis in Colo205 human colon cancer cells in vitro and in vivo. In the present study, we investigated the efficacy of Tan-IIA and 5-fluorouracil (5-FU) in a Colo205 cell xenograft model. For in vivo studies, SCID mice were engrafted with Colo205 cells and from day 10 onwards were randomly divided into 3 groups and treated with 5-FU plus Tan-IIA, 5-FU plus corn oil, and the vehicle alone. At the end of a 4-week dosing schedule, the SCID mice were sacrificed and xenograft tumors were dissected for protein western blot analysis. Our results showed that the Colo205 xenograft model co-treated with Tan-IIA plus 5-FU caused a reduction in the xenograft tumor volumes and decreased P-glycoprotein (P-gp) and microtubule-associated protein light chain 3 (LC3)-II expression compared to 5-FU alone. Based on these observations, it may be possible to develop Tan-IIA plus 5-FU as therapeutic agents for human colon cancer.

摘要

传统中草药被广泛认为是治疗结直肠癌的一种选择。丹参在传统中医中被广泛用于治疗心血管疾病。丹参酮IIA(Tan-IIA)是从丹参中提取的。我们之前的研究表明,Tan-IIA在体外和体内均可诱导Colo205人结肠癌细胞凋亡。在本研究中,我们在Colo205细胞异种移植模型中研究了Tan-IIA和5-氟尿嘧啶(5-FU)的疗效。对于体内研究,将SCID小鼠接种Colo205细胞,从第10天起随机分为3组,分别用5-FU加Tan-IIA、5-FU加玉米油和单独使用赋形剂进行治疗。在为期4周的给药方案结束时,处死SCID小鼠,解剖异种移植肿瘤进行蛋白质免疫印迹分析。我们的结果表明,与单独使用5-FU相比,Tan-IIA加5-FU联合治疗的Colo205异种移植模型导致异种移植肿瘤体积减小,P-糖蛋白(P-gp)和微管相关蛋白轻链3(LC3)-II表达降低。基于这些观察结果,有可能开发Tan-IIA加5-FU作为人类结肠癌的治疗药物。

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