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丹参酮 IIA 对人结肠癌细胞增殖、凋亡和迁移的影响及其机制。

Effects and Mechanism of Tanshinone II A in Proliferation, Apoptosis, and Migration of Human Colon Cancer Cells.

机构信息

China Japan Union Hospital of Jilin University, Changchun, Jilin, China (mainland).

Affiliated Hospital of Changchun University of Traditional Chinese Medicine, Changchun, Jilin, China (mainland).

出版信息

Med Sci Monit. 2019 Jun 28;25:4793-4800. doi: 10.12659/MSM.914446.

Abstract

BACKGROUND The aim of this study was to explore the effect and mechanism of tanshinone II A on proliferation, apoptosis, and migration of human colon cancer cells. MATERIAL AND METHODS CCK-8 approach was carried out to evaluate proliferation after applying various levels of tanshinone II A to SW620 colon carcinoma cells. Flow cytometry (FC) was used to assess apoptosis. Transwell assay was performed to assess invasion in vitro, and the wound-healing assay was applied to assess migration. Western blot analysis was performed to evaluate translation of mTOR, while RT-PCR was carried out to assess transcription of VEGF. RESULTS CCK-8 assay showed that tanshinone II A inhibited SW620 proliferation in comparison to the control group subsequent to 24 h, 48 h, and 72 h (P<0.001). FC revealed that tanshinone II A promoted SW620 apoptosis (P<0.001). The cell migration test revealed that the migration index of cells receiving tanshinone II A decreased. mTOR translation as well as VEGE transcription in cells receiving tanshinone II A was noticeably prohibited compared to control group (P<0.001). CONCLUSIONS Tanshinone II A is able to inhibit proliferation and migration of human colon cancer SW620 cells and promoted cell death. Its mechanism may be by downregulation of mTOR protein and VEGF mRNA.

摘要

背景

本研究旨在探讨丹参酮 IIA 对人结肠癌细胞增殖、凋亡和迁移的影响及其机制。

材料与方法

采用 CCK-8 法检测不同浓度丹参酮 IIA 处理 SW620 结肠癌细胞后的增殖情况。采用流式细胞术(FC)检测细胞凋亡。采用 Transwell 实验评估体外侵袭能力,采用划痕实验评估迁移能力。采用 Western blot 分析检测 mTOR 的翻译,采用 RT-PCR 检测 VEGF 的转录。

结果

CCK-8 实验结果表明,与对照组相比,丹参酮 IIA 处理 24 h、48 h 和 72 h 后可显著抑制 SW620 细胞的增殖(P<0.001)。FC 实验结果表明,丹参酮 IIA 可促进 SW620 细胞凋亡(P<0.001)。细胞迁移实验结果显示,接受丹参酮 IIA 处理的细胞迁移指数降低。与对照组相比,接受丹参酮 IIA 处理的细胞中 mTOR 翻译和 VEGFA 转录明显受到抑制(P<0.001)。

结论

丹参酮 IIA 可抑制人结肠癌细胞 SW620 的增殖和迁移,并促进细胞死亡。其作用机制可能是通过下调 mTOR 蛋白和 VEGF mRNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6010/6612241/1a091e1029b4/medscimonit-25-4793-g001.jpg

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