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Effects of TFPI-2 on Proliferation, Apoptosis and AFP Expression of Hepatocarcinoma Cells |
QIN Xiao-lin1, XU Yong2, FAN Xiao-qing1, LI Wu-xian1, KUANG Wen-bin1, CHENG eng1, TU Zhi-guang1 |
1. Key Laboratory of Laboratory Medical Diagnostics of Education Ministry, Chongqing Medical University, Chongqing 400016, China;
2. Pingshan People's Hospital, Shenzhen 518118, China |
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Abstract Objective: To investigate the effects of tissue factor pathway inhibitor-2 (TFPI-2) gene on the proliferation, apoptosis and expression of alpha fetoprotein of hepatocarcinoma cell line Hep3B. Methods: The recombinant vector of PCDNA3.1-TFPI-2 was transfected into Hep3B cells with liposome, and the cells were selected by G418. The expressions of TFPI-2 mRNA and protein were detected by RT-PCR and Western blot respectively. The influence of TFPI-2 on the proliferation of Hep3B cells via growth curve was assayed by CCK-8 method. The colony-forming unit assay was used to measure single cell self-replication ability. The expression of AFP mRNA was detected by RT-PCR and the AFP secretion of Hep3B cell was measured by electro-chemiluminescence (ECL) immunoassay. Furthermore, the apoptosis was tested by flow cytometry. Results: Expressions of mRNA and protein of TFPI-2 were identified in cells transfected by PCDNA3.1-TFPI-2. The growth rate and self-replication ability of Hep3B cells were significantly lower than those of the two control groups. The inhibition ratio of AFP mRNA expression was 16.51%, and the AFP secretion of Hep3B cells transfected with PCDNA3.1-TFPI-2 was significantly lower than the control groups (P<0.01). The rate of early apoptosis was significantly increased (24.03%±7.28% vs 8.77%±3.66%). Conclusions: The expression of TFPI-2 can simultaneously inhibit the growth and expression of AFP of hepatocarcinoma cells as well as induce early apoptosis.
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Received: 09 August 2011
Published: 25 December 2011
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