Journal of Practical Hepatology ›› 2025, Vol. 28 ›› Issue (4): 497-500.doi: 10.3969/j.issn.1672-5069.2025.04.005

• Hepatitis in vitro and in mice • Previous Articles     Next Articles

Ectonucleotide pyrophosphatase/phosphodiesterase 2 and enhancer of Zeste homolog 2 in HepG2 and HepG2.2.15 cells and their impact on cell proliferation and invasiveness

Deng Wanyu, Huang Zile, Liu Zeyan, et al   

  1. College of Life Science, Shangrao Normal University, Shangrao 334001, Jiangxi Province, China
  • Received:2024-11-17 Online:2025-07-10 Published:2025-07-14

Abstract: Objective The aim of this experiment was to investigate tumor-promoting elements, e.g., ectonucleotide pyrophosphatase/phosphodiesterase 2 (ENPP2) and enhancer of Zeste homolog 2 (EZH2) in HepG2 and HepG2.2.15 cells and their impact on cell proliferation and invasiveness. Methods For inhibition of ENPP2 and EZH2 expression, siRNAs were synthesized, and HepG2, HepG2.2.15, pSM2 plasmid-transfected HepG2(HepG2/pSM2) and siENPP2 or siEZH2-transfected HepG2.2.15 cells were harvested. ENPP2 and EZH2 mRNAs were detected by real-time PCR and their expression was detected by Western blot. Proliferation and invasion of cells were detected by CCK-8 and Trans-well movement. Results ENPP2 and EZH2 mRNA loads in transient HBV-plasmid transfected HepG2 cells or HepG2.2.15 cells with stable HBV infection increased greatly, compared to those in HepG2 cells (P<0.001), and ENPP2 and EZH2 protein expression also intensified (P<0.001); proliferation and invasiveness of HepG2.2.15 cells were obviously elevated compared to in HepG2 cells (P<0.01), while inhibition of ENPP2 or EZH2 expression in HepG2.2.15 cells greatly weakened proliferation and invasiveness of the cells (P<0.01). Conclusion The intensified expressions of ENPP2 and EZH2 in HepG2 cells and in HepG2.2.15 cells might play a pivotal role in carcinogenesis, which needs further investigation.

Key words: HepG2 cells, HepG2.2.15 cells, Ectonucleotide pyrophosphatase/phosphodiesterase 2, Enhancer of Zeste homolog 2, Proliferation, Invasion, In vitro