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.
Download full-text PDF |
Source |
---|
Discov Oncol
December 2024
Department of Ultrasound, The First College of Clinical Medical Sciences, China Three Gorges University, Yichang, 443000, Hubei, China.
Objective: The global incidence of thyroid cancer (THCA) has significantly risen in recent years. This study aims to investigate the role and mechanisms of PTEN in epithelial mesenchymal transition (EMT), invasion and migration of THCA cells.
Methods: PTEN expression in THCA was analyzed through bioinformatics databases.
Ann Med
December 2024
Department of General Surgery (Thyroid Surgery), The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Discov Med
September 2024
Department of Thyroid Surgery, The Second Affiliated Hospital of Nanchang University, 330006 Nanchang, Jiangxi, China.
J Pharmacol Sci
October 2024
Biomedical Research Institute, Hubei University of Medicine, Shiyan City, Hubei Province, PR China; Renmin Hospital, Hubei University of Medicine, Shiyan City, Hubei Province, PR China; Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Shiyan City, Hubei Province, PR China. Electronic address:
The need for novel anti-thyroid cancer (TC) medications is urgent due to the rising incidence and metastatic rates of malignant TC. In this study, we investigated the effect of Polyphyllin VII (PPVII) to TC cells, and explored their potential mechanism. B-CPAP and TPC-1 cells, were used to analyze the antitumor activity of PPVII by quantifying cell growth and metastasis as well as to study the effect on epithelial mesenchymal transition (EMT).
View Article and Find Full Text PDFEur Thyroid J
October 2024
Department of Otorhinolaryngology-Head and Neck Surgery, Gyeongsang National University College of Medicine, Jinju, South Korea.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!