Abstract Title:

Sulforaphane decreases viability and telomerase activity in hepatocellular carcinoma Hep3B cells through the reactive oxygen species-dependent pathway.

Abstract Source:

Cancer Lett. 2010 Sep 28;295(2):260-6. Epub 2010 May 6. PMID: 20451318

Abstract Author(s):

Dong-Oh Moon, Sang-Hyuck Kang, Ki-Cheon Kim, Mun-Ock Kim, Yung Hyun Choi, Gi-Young Kim

Article Affiliation:

Department of Marine Life Sciences, Jeju National University, Republic of Korea.


Sulforaphane (SFN), a dietary isothiocyanate, is a well known natural product that possesses anti-cancer and chemopreventive activities. However, the molecular mechanism of the anti-telomerase activity of SFN is not well understood. In this study, we investigated the hypothesis that SFN inhibits cell viability and telomerase activity via downregulation of telomerase reverse transcriptase (hTERT) expression. We suggest that elevated intracellular reactive oxygen species (ROS) levels, due to exposure to SFN, has a critical role in abolishing since pretreatment with NAC, an antioxidant, resulted in the recovery of hTERT expression. SFN also suppressed the phosphorylation of Akt (Ser-473), thereby inhibiting hTERT phosphorylation and this effect was reversed by pretreatment with NAC. Taken together, these data suggest that ROS are essential for the suppression of SFN-mediated telomerase activity via transcriptional and posttranslational regulation of hTERT.

Study Type : In Vitro Study

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