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Chinese Journal of Hepatic Surgery(Electronic Edition) ›› 2016, Vol. 05 ›› Issue (02): 119-123. doi: 10.3877/cma.j.issn.2095-3232.2016.02.013

Special Issue:

• Basic Researches • Previous Articles     Next Articles

Long noncoding RNA PTENP1 inhibits proliferation and migration of hepatocellular carcinoma cells

Zhiyong Xiong1, Zhicheng Yao2, Weiming Fan1, Mingliang Li3, Kunpeng Hu2, Jianliang Xu1, Yuesi Zhong1, Ruiyun Xu1, Meihai Deng1,()   

  1. 1. Department of Hepatobiliary Surgery, the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China
    2. Department of General Surgery, the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China
    3. Intensive Care Unit, the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China
  • Received:2015-11-11 Online:2016-04-10 Published:2016-04-10
  • Contact: Meihai Deng
  • About author:
    Corresponding author: Deng Meihai,Email:

Abstract:

Objective

To investigate the effect and mechanism of long noncoding RNA (lncRNA) PTEN pseudogene 1 (PTENP1) on the proliferation and migration of hepatocellular carcinoma (HCC) cells.

Methods

Lentiviral vectors expressing PTENP1 were constructed. HCC cells BEL-7404 were infected with LV003-GFP-PTENP1 and control vectors LV003-GFP. BEL-7404 cells stably expressing PTENP1 were constructed and the experimental and control groups were established. The proliferation and clone formation abilities of HCC cells in two groups were detected by CCK-8 assay and clonogenic assay. The migration ability of HCC cells was detected by wound healing assay. The expression of p44/42 mitogen-activated protein kinase (MAPK) and p38 MAPK proteins were detected by Western blot.

Results

The absorbance values A450 of the cells at 48 and 72 h in the experimental group were 1.4±0.3 and 2.3±1.1, significantly lower compared with 3.2±1.7 and 3.4±1.1 in the control group (t=-5.78,-4.23; P<0.05). The number of cell clone formation in the experimental group was 55±12, significantly less than 154±45 in the control group (t= -3.98, P<0.05). The percentage of cell migration in the experimental group was (21.7±2.6)%, significantly lower than (57.7±4.9)% in the control group (t=-8.34, P<0.05). Western blot revealed that the expression of p44/42 MAPK and p38 MAPK proteins in the experimental group was significantly down-regulated compared with those in the control group.

Conclusion

lncRNA PTENP1 can inhibit the proliferation and migration of HCC cells probably through regulating MAPK signaling pathway.

Key words: Ribonucleases, Long non-coding RNA, PTENP1, Liver neoplasms

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