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白术内酯 I 对人肺癌细胞系的抗肿瘤作用。

Anti-tumor effects of atractylenolide I isolated from Atractylodes macrocephala in human lung carcinoma cell lines.

机构信息

Department of Oncology, Chengdu Military General Hospital, Chengdu 610083, Si Chuan Province, China.

出版信息

Molecules. 2013 Oct 29;18(11):13357-68. doi: 10.3390/molecules181113357.

Abstract

Atractylenolide I (ATL-1) is the major sesquiterpenoid of Atractylodes macrocephala. This study was designed to investigate whether ATL-1 induced apoptosis in A549 and HCC827 cells in vitro and in vivo. In our results, ATL-1 significantly decreased the percentage of in vitro viability, in a dose-dependent manner. In addition, DAPI staining and flow cytometry tests demonstrated the induction of apoptosis by ATL-I. Western blot analysis indicated that the protein levels of caspase-3, caspase-9 and Bax were increased in A549 and HCC827 cells after ATL-I exposure; to the contrary, the expressions of Bcl-2, Bcl-XL were decreased after treatment with ATL-1. In the in vivo study, ATL-I effectively suppressed tumor growth (A549) in transplanted tumor nude mice with up-regulation of caspase-3, caspase-9, and Bax and down-regulation of Bcl-2 and Bcl-XL. In conclusion, our results demonstrated that ATL-I has significant antitumor activity in lung carcinoma cells, and the possible mechanism of action may be related to apoptosis induced by ATL-I via a mitochondria-mediated apoptosis pathway.

摘要

白术内酯 I(ATL-1)是白术的主要倍半萜烯。本研究旨在探讨 ATL-1 是否在体外和体内诱导 A549 和 HCC827 细胞凋亡。在我们的结果中,ATL-1 以剂量依赖性方式显著降低体外存活率的百分比。此外,DAPI 染色和流式细胞术试验表明 ATL-I 诱导细胞凋亡。Western blot 分析表明,ATL-1 暴露后 A549 和 HCC827 细胞中 caspase-3、caspase-9 和 Bax 的蛋白水平增加;相反,用 ATL-1 处理后 Bcl-2 和 Bcl-XL 的表达减少。在体内研究中,ATL-1 有效抑制了移植瘤裸鼠(A549)的肿瘤生长,上调了 caspase-3、caspase-9 和 Bax,下调了 Bcl-2 和 Bcl-XL。总之,我们的结果表明 ATL-1 对肺癌细胞具有显著的抗肿瘤活性,其可能的作用机制可能与 ATL-1 通过线粒体介导的凋亡途径诱导细胞凋亡有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e79/6270531/395fde8c7067/molecules-18-13357-g001.jpg

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