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论文摘要

硝呋齐特对甲状腺乳头状癌细胞增殖、迁移及侵袭的影响

Effect of Nifuroxazide on Proliferation, Migration, and Invasion of Thyroid Papillary Carcinoma Cells

作者:胡宇, 梁利波, 张勤等

Author:HU Yu, LIANG Li-bo, ZHANG Qin. et al

收稿日期:          年卷(期)页码:2019,50(1):48-54

期刊名称:四川大学学报(医学版)

Journal Name:JOURNAL OF SICHUAN UNIVERSITY (MEDICAL SCIENCE EDITION)

关键字:甲状腺乳头状癌 硝呋齐特 细胞增殖 细胞迁移 细胞侵袭

Key words:Thyroid cancer Nifuroxazide Proliferation Migration Invasion

基金项目:

中文摘要

目的 探讨硝呋齐特对甲状腺乳头状癌细胞BCPAP和TPC-1的增殖、迁移及侵袭的影响。方法 用不同浓度(0、1.25、2.5、5、10、20 μmol/L)硝呋齐特处理BCPAP和TPC-1细胞,采用MTT法和克隆形成实验观察硝呋齐特对细胞增殖的影响;采用Hoechst 33258染色及流式分选技术观察对细胞凋亡的影响;通过Western blot法检测硝呋齐特处理后BCPAP细胞凋亡相关蛋白及迁移侵袭相关蛋白的表达情况;采用Transwell小室观察细胞迁移和侵袭能力。结果 硝呋齐特0、1.25、2.5 μmol/L处理BCPAP细胞,0、1.25 μmol/L处理TPC-1细胞,24、48、72 h后细胞增殖力均未受到明显抑制( P>0.05);硝呋齐特5、10、20 μmol/L处理BCPAP细胞,10、20 μmol/L处理TPC-1细胞,24、48、72 h后细胞增殖力均受到明显抑制( P P P P P P P P P

英文摘要

Objective To explore the effect of nifuroxazide on proliferation, migration, and invasion of thyroid papillary carcinoma cells. Methods BCPAP and TPC-1 cell lines treated with different concentration (0, 1.25, 2.5, 5, 10, 20 μmol/L) of nifuroxazide, respectively. Cell viability and proliferation of BCPAP and TPC-1 was evaluated by MTT and colony formation assay. Apoptosis analysis and cell nuclear changes were determined by staining with Hoechst 33258 and visualized by a fluorescence microscope after treatment with nifuroxazide. Western blot analysis was used to evaluate protein expressions of apoptosis and invasion of BCPAP cells treated (48 h) with nifuroxazide. Transwell assay was conducted to evaluate ability of cell migration and invasion. Results After being treated with nifuroxazide (0, 1.25, 2.5 μmol/L and 0, 1.25 μmol/L) for 24, 48, 72 h respectively, decreased proliferations of BCPAP and TPC-1 cell lines were not obvious ( P>0.05). However, treated BCPAP and TPC-1 cells with higher concentration respectively (5, 10, 20 μmol/L and 5,10 μmol/L) of nifuroxazide for 24, 48, 72 h, the inhibitory effects were significantly obvious ( P P P P P P P P Pin vitro, and blocks migration and invasion of cells in vitro by reducing protein expressions of MMP-2 and MMP-9.

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