Tianjin Medical Journal ›› 2023, Vol. 51 ›› Issue (7): 707-712.doi: 10.11958/20221545

• Cell and Molecular Biology • Previous Articles     Next Articles

Effects of taurine on proliferation, apoptosis and migration of human pancreatic cancer cell lines BxPC-3 and PANC-1

GAO Huijie1(), LI Qian2, TIAN Bin3, ZHU Riming1, LIU Chao1,()   

  1. 1 College of Pharmacy, Jining Medical University, Rizhao 276827, China
    2 Pharmacy Department, Qingdao Women and Children's Hospital
    3 Clinical Laboratory, People’s Hospital of Rizhao
  • Received:2022-10-21 Revised:2023-02-22 Published:2023-07-15 Online:2023-07-18
  • Contact: LIU Chao E-mail:lcanatomy@163.com

Abstract:

Objective To investigate the effects of taurine (Tau) on the proliferation, apoptosis and migration of pancreatic cancer ductal cells. Methods BxPC-3 and PANC-1 cells were cultured in vitro and pretreated with different concentrations of Tau (0, 10, 20, 40, 80, 160 mmol/L). Cell counting kit-8 (CCK-8), cell scratch assay and Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) method were used to observe the effect of Tau on the proliferation, migration and apoptosis of BxPC-3 and PANC-1 cells. Quantitative real-time polymerase chain reaction (qPCR) and Western blot assay were used to detect the effect of Tau on mRNA and protein expression of relevant apoptosis and cell cycle molecules in BxPC-3 and PANC-1 cells. Results Tau significantly inhibited the proliferation and migration activities of BxPC-3 and PANC-1, and Tau could promote the apoptosis of BxPC-3 and PANC-1 cells. Compared with the control group, expression levels of P53, P21 and BAX in BxPC-3 cells treated with Tau showed a significant upward trend, while the expression of PCNA was significantly decreased. The expression levels of Bcl-2, PCNA, CyclinA2, CyclinB1, CyclinE, CDK1, CDK2, CDK4 and CDK6 in PANC-1 cells were significantly lower than those in the normal control group, while the expression levels of P53 and P21 showed an upward trend. Conclusion Tau can inhibit the proliferation and migration activity of BxPC-3 and PANC-1 pancreatic cancer cells, and promote cell apoptosis, possibly by affecting related apoptosis genes and cyclins.

Key words: Taurine, pancreatic neoplasms, tumor suppressor protein p53, cyclin-dependent kinase inhibitor p21, cyclins, cyclin-dependent kinase

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