Chemoprevention by lipid-soluble tea polyphenols in diethylnitrosamine/phenobarbital-induced hepatic pre-cancerous lesions

Ting Shen, Soo Chin Khor, Fan Zhou, Ting Duan, Yu Ying Xu, Yi Fan Zheng, Stephen Hsu, Jamie Ann De Stefano, Jun Yang, Li Hong Xu, Xin Qiang Zhu

Research output: Contribution to journalArticlepeer-review

9 Scopus citations


Background: Green tea polyphenols (GTPs) have been proposed as promising candidates for chemoprevention. However, GTPs levels are maintained relatively low in the blood and are chemically-unstable. Lipid-soluble tea polyphenols (LTPs) are products of modified GTPs with ester linkage with fatty acids. LTPs are lipophilic and expected to provide improved absorption and utilization in the body compared with water-soluble polyphenols. The current study was designed to investigate the chemo-preventive property and the possible mechanisms of LTP action against diethylnitrosamine (DEN)-induced liver cancer in rats. Materials and Methods: Oral administration of LTPs at doses of 0, 40, and 400 mg/kg/day was initiated 2 weeks prior to DEN injection and was continued for 30 weeks. At that time point samples were collected and liver histopathological analyses were performed. Results: LTPs decreased the area and number of placental glutathione S-transferase-positive foci in liver samples of DEN-treated rats. Furthermore, LTPs counteracted DEN-induced fibrosis formation in liver. Immunohistochemical staining of rat liver showed that LTPs inhibited DEN-mediated elevations in numbers of cells positive for PCNA and 8-OHdG. Conclusion: For the first time, the present study demonstrated, that LTPs exert a chemo-preventive effect against precancerous lesions through inhibition of cellular proliferation and DNA damage in a rat liver model.

Original languageEnglish (US)
Pages (from-to)683-694
Number of pages12
JournalAnticancer research
Issue number2
StatePublished - Feb 1 2014


  • DNA damage
  • GTPs
  • LTPs
  • Precancerous lesions
  • Proliferation

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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