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穿心莲内酯抑制SGC7901胃癌细胞的增殖和转移。

Andrographolide Inhibits Proliferation and Metastasis of SGC7901 Gastric Cancer Cells.

作者信息

Dai Lei, Wang Gang, Pan Wensheng

机构信息

Department of Gastroenterology, Tongde Hospital of Zhejiang Province, Hangzhou, Zhejiang, China; Department of Gastroenterology, The Second Affiliated Hospital, Zhejiang University, School of Medicine, Hangzhou, Zhejiang, China.

Department of Gastroenterology, Tongde Hospital of Zhejiang Province, Hangzhou, Zhejiang, China; Tumor Institute of Integrative Medicine, Zhejiang Provincial Academy of Traditional Chinese Medicine, Tongde Hospital of Zhejiang Province, Hangzhou, Zhejiang, China.

出版信息

Biomed Res Int. 2017;2017:6242103. doi: 10.1155/2017/6242103. Epub 2017 Jan 18.

Abstract

To explore the mechanisms by which andrographolide inhibits gastric cancer cell proliferation and metastasis, we employed the gastric cell line SGC7901 to investigate the anticancer effects of andrographolide. The cell survival ratio, cell migration and invasion, cell cycle, apoptosis, and matrix metalloproteinase activity were assessed. Moreover, western blotting and real-time PCR were used to examine the protein expression levels and the mRNA expression levels, respectively. The survival ratio of cells decreased with an increasing concentration of andrographolide in a dose-dependent manner. Consistent results were also obtained using an apoptosis assay, as detected by flow cytometry. The cell cycle was blocked at the G2/M2 phase by andrographolide treatment, and the proportion of cells arrested at G1/M was enhanced as the dose increased. Similarly, wound healing and Transwell assays showed reduced migration and invasion of the gastric cancer cells at various concentrations of andrographolide. Andrographolide can inhibit cell proliferation, invasion, and migration, block the cell cycle, and promote apoptosis in SGC7901 cells. The mechanisms may include upregulated expression of Timp-1/2, cyclin B1, p-Cdc2, Bax, and Bik and downregulated expression of MMP-2/9 and antiapoptosis protein Bcl-2.

摘要

为探究穿心莲内酯抑制胃癌细胞增殖和转移的机制,我们采用胃癌细胞系SGC7901来研究穿心莲内酯的抗癌作用。评估了细胞存活率、细胞迁移和侵袭、细胞周期、凋亡以及基质金属蛋白酶活性。此外,分别使用蛋白质印迹法和实时定量PCR检测蛋白表达水平和mRNA表达水平。随着穿心莲内酯浓度的增加,细胞存活率呈剂量依赖性降低。通过流式细胞术检测的凋亡试验也得到了一致的结果。穿心莲内酯处理使细胞周期阻滞在G2/M期,且随着剂量增加,阻滞在G1/M期的细胞比例增加。同样,伤口愈合试验和Transwell试验表明,在不同浓度的穿心莲内酯作用下,胃癌细胞的迁移和侵袭能力降低。穿心莲内酯可抑制SGC7901细胞的增殖、侵袭和迁移,阻滞细胞周期并促进其凋亡。其机制可能包括Timp-1/2、细胞周期蛋白B1、p-Cdc2、Bax和Bik的表达上调,以及MMP-2/9和抗凋亡蛋白Bcl-2的表达下调。

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