Incomplete radiofrequency ablation promotes the development of CD133+ cancer stem cells in hepatocellular carcinoma cell line HepG2 via inducing SOX9 expression

Hepatobiliary Pancreat Dis Int. 2018 Oct;17(5):416-422. doi: 10.1016/j.hbpd.2018.09.012. Epub 2018 Sep 15.

Abstract

Background: Cancer stem cells (CSCs) accelerate the growth of hepatocellular carcinoma (HCC) residual after incomplete radiofrequency ablation (In-RFA). The present study aimed to detect the effects of In-RFA on stemness transcription factors (STFs) expression which are important for the production and function of CSCs, and to find which STFs promote HCC stemness after In-RFA.

Methods: HepG2 cells were used for in vitro and in vivo studies. Flow cytometry and sphere-formation assays were used to detect the level and function of CD133+CSCs in the models. PCR array and ELISA were applied to analyze the altered expression of 84 STFs in CD133+CSCs in two models. Specific lentiviral shRNA was used to knockdown STFs expression, followed by detecting In-RFA's effects on the levels and function of CD133+CSCs.

Results: In-RFA was identified to induce CD133+CSCs and increase their tumorigenesis ability in vitro and in vivo. The mRNA levels of 84 STFs in CD133+CSCs were detected by PCR array, showing that 15 and 22 STFs were up-regulated in two models, respectively. Meanwhile, the mRNA levels of seven common STFs were up-regulated in both models. ELISA assay demonstrated that only the protein of sex determining region Y-box 9 (SOX9) was up-regulated in both models, the protein levels of the other 6 common STFs did not increase in both models. Finally, SOX9 was identified to play an important role in inducing, maintaining stemness and promoting tumorigenesis ability of CD133+CSCs in both models.

Conclusion: In-RFA-induced SOX9 stimulates CD133+CSCs proliferation and increases their tumorigenesis ability, suggesting that SOX9 may be a good target for HCC treatment.

Keywords: Cancer stem cells; HepG2; Hepatocellular carcinoma; Radiofrequency ablation.

MeSH terms

  • AC133 Antigen / genetics*
  • Animals
  • Carcinogenesis / genetics*
  • Carcinoma, Hepatocellular / pathology
  • Carcinoma, Hepatocellular / surgery*
  • Cell Line, Tumor
  • Cell Proliferation
  • Cell Survival / genetics
  • Enzyme-Linked Immunosorbent Assay
  • Flow Cytometry / methods
  • Gene Expression Regulation, Neoplastic / genetics*
  • Hep G2 Cells
  • Humans
  • Immunoblotting / methods
  • In Vitro Techniques
  • Liver Neoplasms / pathology
  • Liver Neoplasms / surgery*
  • Mice
  • Mice, Knockout
  • Neoplastic Stem Cells
  • Polymerase Chain Reaction / methods
  • RNA, Messenger / analysis
  • Radiofrequency Ablation / methods
  • SOX9 Transcription Factor / genetics*
  • Sensitivity and Specificity
  • Signal Transduction
  • Up-Regulation

Substances

  • AC133 Antigen
  • Prom1 protein, mouse
  • RNA, Messenger
  • SOX9 Transcription Factor
  • Sox9 protein, mouse