[Relationship between polymerase eta expression and DNA damage-tolerance in human hepatic cells by hydroquinone]

Zhonghua Yu Fang Yi Xue Za Zhi. 2009 Jan;43(1):56-60.
[Article in Chinese]

Abstract

Objective: To investigate the effects of hydroquinone (HQ) on expression of Polymerase eta (Pol eta) and DNA damage in human hepatic cells (L-02), and to explore the role and possible mechanism of Pol eta involved in the process of DNA damage-tolerance.

Methods: After L-02 hepatic cells were exposed to HQ with various concentrations (0, 5, 10, 20, 40, 80 and 160 micromol/L) for 24 h, cell survival rate was detected by MTT assay; DNA impairment was detected by single cell gel electrophoresis (SCGE); Real-time fluorescent quantitative PCR and Western blotting methods were used to measure the expression of Pol eta at the mRNA and protein level in L-02 hepatic cells exposed to HQ with various concentrations (0, 5, 10, 20, 40, 80 and 160 micromol/L).

Results: MTT assay showed that HQ with concentrations from 0 to 80 micromol/L had little effect on the survival rate of L-02 (P>0.05); whereas the survival rate of the group of 160 micromol/Lwas significantly higher than that of the control (P<0.01) after being treated with HQ for 24 h; the higher dose of HQ presented, the more degrees of DNA damage were produced. It was found that HQ in a low concentration (1-80 micromol/L) could induce the expression of Pol eta which was in proportion to the increasements of HQ concentration; the expression levels of mRNA and protein were reached to the maximum when treated with 80 micromol/L; the expression of Pol eta decreased (the relative quantity values were 2.32 +/- 0.16 and 1.20 respectively) once the concentration of HQ exceeded 160 micromol/L as compared with the group of 80 micromol/L, but it was higher than that of the control.

Conclusion: This study suggested that Pol eta might involve in the process of DNA damage-tolerance induced by HQ in the hepatic cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Survival / drug effects
  • Cells, Cultured
  • DNA Damage / drug effects*
  • DNA Repair
  • DNA-Directed DNA Polymerase / metabolism*
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism*
  • Humans
  • Hydroquinones / adverse effects*
  • Mutagens

Substances

  • Hydroquinones
  • Mutagens
  • DNA-Directed DNA Polymerase
  • Rad30 protein
  • hydroquinone