1. 广州医科大学药学院,广东省分子靶标与临床药理重点实验室,广东,广州,511436
2. 广州医科大学生命科学学院,广东,广州,511436
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雷雪萍, 钟怡行, 邓秋狄, 等. 扁蒴藤素抑制NCI-H1299细胞迁移侵袭的作用与机制研究[J]. 上海中医药杂志, 2020,54(12):79-83.
LEI Xueping, ZHONG Yihang, DENG Qiudi, et al. Effect and underlying mechanism of pristimerin on migration and invasion of NCI-H1299 cells[J]. Shanghai Journal of Traditional Chinese Medicine, 2020,54(12):79-83.
雷雪萍, 钟怡行, 邓秋狄, 等. 扁蒴藤素抑制NCI-H1299细胞迁移侵袭的作用与机制研究[J]. 上海中医药杂志, 2020,54(12):79-83. DOI: 10.16305/j.1007-1334.2021.2008045.
LEI Xueping, ZHONG Yihang, DENG Qiudi, et al. Effect and underlying mechanism of pristimerin on migration and invasion of NCI-H1299 cells[J]. Shanghai Journal of Traditional Chinese Medicine, 2020,54(12):79-83. DOI: 10.16305/j.1007-1334.2021.2008045.
目的:探讨扁蒴藤素对非小细胞肺癌NCI-H1299细胞迁移侵袭的抑制作用及其分子机制。 方法:采用不同浓度(0~80 μmol/L)的扁蒴藤素处理NCI-H1299细胞,CCK-8法检测细胞增殖的情况,确定扁蒴藤素对NCI-H1299细胞的非毒剂量,并以此作为后续的药效与分子机制研究剂量。划痕实验评价扁蒴藤素对NCI-H1299细胞横向迁移能力的影响;transwell迁移与侵袭实验评价扁蒴藤素对NCI-H1299细胞纵向迁移能力与侵袭能力的影响;免疫印迹法与荧光定量PCR实验分别测定上皮-间充质相关标记物蛋白与mRNA的表达水平。 结果:扁蒴藤素浓度<2.5 μmol/L时,对NCI-H1299细胞无明显的细胞毒性。与空白对照组比较,非毒剂量的扁蒴藤素(0.5 μmol/L、1.0 μmol/L和2.0 μmol/L)可明显抑制NCI-H1299细胞的横向迁移以及纵向的迁移与侵袭能力(P<0.01)。扁蒴藤素处理后,上皮细胞标记物E-cadherin与ZO1的表达水平明显升高,间充质细胞标记物N-caherin与Vimentin的表达水平明显降低(P<0.01)。 结论:扁蒴藤素具有抑制NCI-H1299细胞迁移与侵袭的能力,且这一作用可能与其调控NCI-H1299细胞的上皮-间充质转化相关。
Objective:To evaluate the effect of pristimerin on the migration and invasion of non-small cell lung cancer(NSCLC)NCI-H1299 cells,and explore the underlying mechanism. MethodsNCI-H1299 cells were treated with different concentrations of pristimerin (0~80 μmol/L). The proliferation of NCI-H1299 cells was detected by cell counting kit (CCK-8) assay, and the non-toxic dose of pristimerin to NCI-H1299 cells was determined, which was used as the follow-up dose for the study of pharmacodynamics and molecular mechanism. The effect of pristimerin on the lateral migration ability of NCI-H1299 cells was evaluated by wound-healing assay; the effect of pristimerin on the longitudinal migration and invasion ability of NCI-H1299 cells was evaluated by transwell migration and invasion assay; the protein and mRNA expression levels of epithelial-mesenchymal related markers were measured by Western blot and real-time quantification PCR assay, respectively. Results:When the concentration of pristimerin was less than 2.5 μmol/L, it had no obvious cytotoxicity to NCI-H1299 cells. Compared with the blank control group, the non-toxic dose of pristimerin (0.5 μmol/L, 1.0 μmol/L and 2.0 μmol/L) could significantly inhibit the lateral migration and longitudinal migration and invasion of NCI-H1299 cells (P<0.01). After treatment with pristimerin, the expression levels of epithelial markers E-cadherin and ZO1 were significantly increased, while the expression levels of mesenchymal cell markers N-caherin and Vimentin were significantly decreased (P< 0.01). Conclusion: Pristimerin can inhibit the migration and invasion of NCI-H1299 cells, and this effect may be related to the regulation of epithelial-mesenchymal transformation of NCI-H1299 cells.
扁蒴藤素非小细胞肺癌肿瘤细胞迁移肿瘤细胞侵袭上皮-间充质转化
pristimerinnon-small cell lung cancer(NSCLC)cancer cells migrationcancer cells invasionepithelial-mesenchymal transformation
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