alexa Alpha Fetoprotein Plays Antagonistic Role in Benzyl-Iso
ISSN: 2167-7700

Chemotherapy: Open Access
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Research Article

Alpha Fetoprotein Plays Antagonistic Role in Benzyl-Isothiocyanate Arresting Cell Cycle in Liver Cancer Cells

Mingyue Zhu1,2,3, Wei Li1,2, Xu Dong1,2, Peng Zhou3, Junli Guo1 and Mengsen Li1,2,4*

1Hainan Provincial Key Laboratory of Carcinogenesis and Intervention, Hainan Medical College, Haikou 571199, Hainan Province, P.R. China

2Key Laboratory of Molecular Biology, Hainan Medical College, Haikou 571199, Hainan Province, P.R. China

3Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Science, Haikou 571199, Hainan Province, P.R. China

4Tumor Institution of Hainan Medical College, Haikou 570102, Hainan Province, PR. China

*Corresponding Author:
Mengsen Li
Hainan Provincial Key Laboratory of Carcinogenesis and Intervention
Hainan Medical College, Haikou 571199, Hainan Province, P.R. China
Tel: +86-898-66895322
E-mail: [email protected]

Received date: January 21, 2016 Accepted date: February 29, 2016 Published date: March 06, 2016

Citation: Zhu M, Li W, Dong X , Zhou P, Guo J, et al. (2016) Alpha Fetoprotein Plays Antagonistic Role in Benzyl-Isothiocyanate Arresting Cell Cycle in Liver Cancer Cells. Chemo Open Access 5: 195. doi:10.4172/2167-7700.1000195

Copyright: © 2016 Zhu M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

Background: To investigate the effect of alpha fetoprotein (AFP) on benzyl-isothiocyanate (BITC) arresting cell cycle in human liver cancer cells line in vitro, and explore the possible role mechanism of BITC inhibited proliferation of hepatocellular carcinoma (HCC) cells. Methods: In this study, we selected HCC cells lines, Bel 7402 and HLE for test. Fluorescent microscopy and Western blotting were applied to observe the transfected effect and expression of proteins; MTT assay the proliferation of HCC cells; Flow cytometry method was used to detect the cellular cycle; RNA interference was used to test and expressed vector constructed technology were performed to silence and induce expression of AFP, respectively. Results: Analysis showed BITC had a significant inhibitory effect on the proliferation of HCC cells in dosedependent manner, inhibitory effect was enhanced while Bel 7402 cells were transfected with AFP-siRNA vectors but attenuated in HLE cells while transfected with pcDNA3.1-afp vectors. The growth ratio of AFP-siRNA transfected Bel 7402 cells and pcDNA3.1-afp transfected HLE cells followed treated with 80 μmol/L BITC were (42.43 ± 4.92)% (P<0.05 vs Bel 7402 cells group) and (40.13 ± 4.99)% (P<0.05 vs HLE cells group). BITC could obviously induce cell cycle G2/M phase arrest in theses HCC cells; The induction effect was enhanced in AFP-siRNA transfected Bel 7402 cells but attenuated in pcDNA3.1-afp transfected HLE cells. BITC inhibited the expression of cell cycle related proteins, cyclin B1, CDK1, Cdc25c but stimulated expression of Weel in Bel 7402 cells and HLE cells, and such effect was enhanced in AFP-siRNA transfected Bel 7402 cells but attenuated in pcDNA3.1-afp transfected HLE cells. Conclusions: BITC could inhibit the growth of HCC cells and induce cell cycle G2/M phase arrest through down regulating the expression of cyclin B1, CDK1, Cdc25c and up regulating the expression of Weel; AFP played an antagonistic role in BITC arresting cell cycle in HCC cells.

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