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[硝呋太尔对甲状腺乳头状癌细胞增殖、迁移和侵袭的影响]

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

作者信息

Hu Yu, Liang Li-Bo, Zhang Qin, Lan Fei, Lin Ken, He He, Li Shuang-Qing

机构信息

Departmant of Endocrinology and Metabolism, Chengdu First People's Hospital, Montpellier France-Chengdu China Research Institution of Endocrine and Metabolic Diseases, Chengdu 610041, China.

Department of General Practice, West China Hospital, Sichuan University, Chengdu 610041, China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2019 Jan;50(1):48-54.

Abstract

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 ( >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 ( <0.05), and the inhibitory effects were increased in a CM(155mm]concentration- and time-dependent manner. The inhibition in proliferation of TPC-1 cell with nifuroxazide (2.5, CM)]5 μmol/L) took effect from 72 h and 48 h ( <0.05), respectively. Clone formations of BCPAP and TPC-1 cells were significantly inhibited after being exposed to nifuroxazide (2.5, 5 μmol/L) for 10 d ( <0.05). Hoechst 33258 staining assay showed that nifuroxazide (10 μmol/L) treatment resulted in cell shrinking, nuclear fragmentation and formation of condensed nuclei with bright-blue fluorescence. After 48 h, the percentage of apoptotic cells of BCPAP and TPC-1 significantly increased respectively as the concentration of nifuroxazide with 10 μmol/L ( <0.005). Pro-apoptotic protein CC-3 and Bax expression levels increased significantly ( <0.05), and the expression of anti-apoptotic protein Bcl-2 decreased significantly ( <0.05) in BCPAP cells after nifuroxazide-treatment (10 μmol/L) for 48 h. The percentage of migrations and invasions of BCPAP and TPC-1 significantly decreased ( <0.05) in the presence of nifuroxazide (10 μmol/L, 48 h). Nifuroxazide (10 μmol/L) treatment significantly decreased the expressions of matrix metalloproteinase (MMP)-2 and MMP-9 in BCPAP cells ( <0.05) . Expression of MMPs family inhibitor-tissue inhibitors of metalloproteinase (TIMP)-2 increased ( <0.05).

CONCLUSION

Nifuroxazide inhibits the proliferation of thyroid cancer cells BCPAP and TPC-1, induceds the cell apoptosis by up-regulating the expressions of CC-3 and Bax proteins , and blocks migration and invasion of cells by reducing protein expressions of MMP-2 and MMP-9.

摘要

目的

探讨硝呋齐特对甲状腺乳头状癌细胞增殖、迁移和侵袭的影响。

方法

分别用不同浓度(0、1.25、2.5、5、10、20 μmol/L)的硝呋齐特处理BCPAP和TPC-1细胞系。通过MTT和集落形成试验评估BCPAP和TPC-1的细胞活力和增殖情况。用Hoechst 33258染色并经荧光显微镜观察,测定硝呋齐特处理后的细胞凋亡分析和细胞核变化。采用蛋白质免疫印迹分析评估经硝呋齐特处理(48小时)的BCPAP细胞凋亡和侵袭相关蛋白的表达。进行Transwell试验评估细胞迁移和侵袭能力。

结果

分别用硝呋齐特(0、1.25、2.5 μmol/L和0、1.25 μmol/L)处理BCPAP和TPC-1细胞系24、48、72小时后,BCPAP和TPC-1细胞系增殖降低不明显(>0.05)。然而,分别用较高浓度(5、10、20 μmol/L和5、10 μmol/L)的硝呋齐特处理BCPAP和TPC-1细胞24、48、72小时,抑制作用显著(<0.05),且抑制作用呈浓度和时间依赖性增加。硝呋齐特(2.5、5 μmol/L)对TPC-1细胞增殖的抑制作用分别在72小时和48小时开始起效(<0.05)。用硝呋齐特(2.5、5 μmol/L)处理BCPAP和TPC-1细胞10天后,克隆形成显著受到抑制(<0.05)。Hoechst 33258染色试验显示,硝呋齐特(10 μmol/L)处理导致细胞皱缩、核碎裂并形成亮蓝色荧光的凝聚核。48小时后,硝呋齐特浓度为10 μmol/L时,BCPAP和TPC-1细胞的凋亡率分别显著增加(<0.005)。硝呋齐特(10 μmol/L)处理48小时后,BCPAP细胞中促凋亡蛋白CC-3和Bax的表达水平显著升高(<0.05),抗凋亡蛋白Bcl-2的表达显著降低(<0.05)。在硝呋齐特(10 μmol/L,48小时)存在的情况下,BCPAP和TPC-1的迁移和侵袭率显著降低(<0.05)。硝呋齐特(10 μmol/L)处理显著降低了BCPAP细胞中基质金属蛋白酶(MMP)-2和MMP-9的表达(<0.05)。MMPs家族抑制剂——金属蛋白酶组织抑制剂(TIMP)-2的表达增加(<0.05)。

结论

硝呋齐特抑制甲状腺癌细胞BCPAP和TPC-1的增殖,通过上调CC-3和Bax蛋白的表达诱导细胞凋亡,并通过降低MMP-2和MMP-9的蛋白表达来阻断细胞的迁移和侵袭。

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