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TM6SF2基因的E167K多态性影响肝癌细胞HEPA 1-6的细胞周期。

E167K polymorphism of TM6SF2 gene affects cell cycle of hepatocellular carcinoma cell HEPA 1-6.

作者信息

Du Shuixian, Lu Linlin, Miao Yingxia, Jin Wenwen, Li Changfei, Xin Yongning, Xuan Shiying

机构信息

Medical College of Qingdao University, Qingdao, 266071, China.

Department of Gastroenterology, Qingdao Municipal Hospital, 1 Jiaozhou Road, Qingdao, Shandong Province, 266011, China.

出版信息

Lipids Health Dis. 2017 Apr 13;16(1):76. doi: 10.1186/s12944-017-0468-8.

Abstract

BACKGROUND

Some studties reported that the polymorphism of TM6SF2 gene E167K affects the occurrence and the progression of hepatocytes carcinoma (hepatocellular, HCC). In oeder to investigate the effects of the polymorphism of TM6SF2 gene E167K in the pathogenesis of HCC, we explored its influence on the cell cycle in hepatocellular carcinoma cell HEPA1-6.

METHODS

HEPA 1-6 cells which could respectively overexpress TM6SF2 wild type and E167K variant were cultured and HEPA 1-6 cells with zero load plasmids were used as matched control. Flow cytometry was used to detect the cell cycles of these 3 type of HEPA 1-6 cells. Realtime fluores-cence quantitative PCR and western blot were used to analyzed the expression of regulatory factors (Cyclin D1、p53、P16、P27、P21 and Rb) of cell cycle. T-test was used in statistical analysis.

RESULTS

Cell cycle phase distribution was presented by the proportion of cells in each phases (%). Compared with the control group, the cell cycle phase distribution (G phase 57.36 ± 0.21%, G/M phase 25.61 ± 0.36%,S phases 19.31 ± 0.25%) had no differences in wild type group (G phase 57.63 ± 0.28%, G/M phase 25.77 ± 0.51%, S phases 19.54 ± 0.25%; P < 0.05). Between variant type group and wild type group,G phase was significantly decreased (variant type group G phase 36.26 ± 0.31%, P < 0.05),S phase and G/M phase were increased(variant type group S phase 28.41 ± 0.31%, P < 0.05;G/M phase 35.23 ± 0.14%, P < 0.05), respectively. Compared with control group,the relative expression of CyclinD1、P53 and Rb mRNA in variant type group was significantly upregulated (2.03 ± 0.01 VS 1.04 ± 0.06, 1.88 ± 0.05 VS 1.37 ± 0.03, 1.29 ± 0.06 VS 1.15 ± 0.03, P < 0.05) and P27 mRNA in variant type group was significantly downregulated (0.56 ± 0.02 VS 0.85 ± 0.05, P < 0.05). Compared with wild type group, the relative expression of CyclinD1、P53 and Rb mRNA in variant type group was significantly upregulated (wild type group 1.00 ± 0.00, 1.48 ± 0.09, 1.18 ± 0.01, P < 0.05) and P27 mRNA in variant type group was significantly downregulated (variant type group 0.82 ± 0.05,P < 0.05). There was no statistical significance between wild type group and control group (P > 0.05). P16 and P21 expression showed no statistical sigtfificance in any of these three groups (P > 0.05).

CONCLUSION

E167K polymorphism of TM6SF2 gene affects cell cycles of HEPA1-6 cells via up-regulating CyclinD1、P53 and Rb and down-regulating P27.

摘要

背景

一些研究报道,TM6SF2基因E167K多态性影响肝细胞癌(HCC)的发生和进展。为了研究TM6SF2基因E167K多态性在HCC发病机制中的作用,我们探讨了其对肝癌细胞HEPA1-6细胞周期的影响。

方法

培养分别过表达TM6SF2野生型和E167K变体的HEPA 1-6细胞,将空载质粒的HEPA 1-6细胞作为匹配对照。采用流式细胞术检测这3种类型HEPA 1-6细胞的细胞周期。采用实时荧光定量PCR和蛋白质印迹法分析细胞周期调节因子(细胞周期蛋白D1、p53、P16、P27、P21和Rb)的表达。采用t检验进行统计学分析。

结果

细胞周期阶段分布以各阶段细胞所占比例(%)表示。与对照组相比,野生型组细胞周期阶段分布(G期57.36±0.21%,G/M期25.61±0.36%,S期19.31±0.25%)无差异(野生型组G期57.63±0.28%,G/M期25.77±0.51%,S期19.54±0.25%;P>0.05)。变异型组与野生型组相比,G期显著降低(变异型组G期36.26±0.31%,P<0.05),S期和G/M期分别升高(变异型组S期28.41±0.31%,P<0.05;G/M期35.23±0.14%,P<0.05)。与对照组相比,变异型组细胞周期蛋白D1、p53和Rb mRNA的相对表达显著上调(2.03±0.01对1.04±0.06,1.88±0.05对1.37±0.03,1.29±0.06对1.15±0.03,P<0.05),变异型组P27 mRNA的相对表达显著下调(0.56±0.02对0.85±0.05,P<0.05)。与野生型组相比,变异型组细胞周期蛋白D1、p53和Rb mRNA的相对表达显著上调(野生型组1.00±0.00,1.48±0.09,1.18±0.01,P<0.05),变异型组P27 mRNA的相对表达显著下调(变异型组0.82±0.05,P<0.05)。野生型组与对照组之间无统计学意义(P>0.05)。P16和P21表达在这三组中均无统计学意义(P>0.05)。

结论

TM6SF2基因E167K多态性通过上调细胞周期蛋白D1、p53和Rb以及下调P27影响HEPA1-6细胞的细胞周期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b150/5390375/7fa4f36e6e15/12944_2017_468_Fig1_HTML.jpg

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