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Chinese Journal of Clinicians(Electronic Edition) ›› 2018, Vol. 12 ›› Issue (08): 456-461. doi: 10.3877/cma.j.issn.1674-0785.2018.08.006

Special Issue:

• Clinical Research • Previous Articles     Next Articles

Role of lincRNA ULK4P2 in biological behavior of hepatocellular carcinoma cells

Tingting Yu1, Fei Chen1, Hongshan Yang1, Jun Li1,()   

  1. 1. Department of Oncology, Xiaogan Hospital Affiliated to Wuhan University of Science and Technology, Xiaogan 432000, China
  • Received:2018-02-02 Online:2018-04-15 Published:2018-04-15
  • Contact: Jun Li
  • About author:
    Corresponding author: Li Jun, Email:

Abstract:

Objective

To investigate the role of the long-strand intergenic non-coding RNA (lincRNA) ULK4P2 in the biological behavior of hepatocellular carcinoma cells by interfering with the expression of lincRNA ULK4P2 in hepatocellular carcinoma cell lines.

Methods

Real-time quantitative polymerase chain reaction (RT-qPCR) was used to detect the expression of lincRNA ULK4P2 in different hepatoma cell lines and normal cells. According to the results of RT-qPCR, hepatocellular carcinoma cell line HepG2 was selected for subsequent interference experiments. Small interfering RNA (siRNA) targeting lincRNA ULK4P2, including siRNA-1, siRNA-2, and siRNA-3, as well as siRNA-mock (blank control) and siRNA-Scramble (reconstructed after shuffling the siRNA sequence of interest; negative control) were transfected into HepG2 cells, and siRNA-2 was selected for subsequent experiments according to the interference effect on lincRNA ULK4P2. The expression of lincRNA ULK4P2 in HepG2 cells was down-regulated by siRNA-mediated interference. The role of lincRNA ULK4P2 expression in the proliferation of hepatoma cells was studied by CCK-8 assay. Flow cytometry was used to detect the expression of lincRNA ULK4P2 and the influence on apoptosis and cell cycle distribution of liver cancer cells. One-way analysis of variance was used to compare the proliferation activity (absorbance) and cell cycle distribution of HepG2 cells transfected with siRNA-2, siRNA-mock, or siRNA-Scramble.

Results

Compared with the siRNA-mock group and siRNA-Scramble group, the proliferation of hepatocellular carcinoma cells was significantly inhibited after the down-regulation of lincRNA ULK4P2 in the siRNA-2 group (P<0.05). After down-regulating the expression of lincRNA ULK4P2 in HepG2 cells, there was no significant change in the number of cells in each phase. The proportion of G2/M phase cells in the siRNA-2 group (43.92%) was significantly higher than that in the siRNA-mock group (7.81%) and siRNA-Scramble group (8.21%) (P<0.05).

Conclusion

Our findings indicate that lincRNA ULK4P2 may be involved in the proliferation of hepatocellular carcinoma cells .

Key words: Long intergenic non-coding RNA ULK4P2, Hepatocellular carcinoma, Mechanism

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