Submitted to: Meeting Abstract
Publication Type: Abstract only
Publication Acceptance Date: 9/15/2010
Publication Date: 10/22/2010
Citation: Zeng, H., Trujillo, O., Moyer, M.P., Botnen, J.H. 2010. Sulforaphane plays common and different roles in tumorigenic and nontumorigenic colon cell growth [abstract]. American Institute for Cancer Research . Poster No. 40. Interpretive Summary:
Technical Abstract: Sulforaphane (SFN) is a naturally occurring member of the isothiocyanate family of chemopreventive agents and the induction of cell cycle arrest and apoptosis is a key mechanism by which SFN exerts its colon cancer prevention. However, little is known about the differential effects of SFN on colon cancer and normal cells. In this study, we demonstrated that prolonged SFN (5, 10 or 15 umol/L) exposure (72 h) inhibited cell proliferation up to 95% in colon cancer cells (HCT116) and 52% in normal colon mucosa-derived (NCM460) cells, respectively. Our data also showed that prolonged SFN exposure led to the significant induction of apoptosis and G2/M cell cycle arrest in HCT116, but to a much lesser extent in NCM460 cells. Furthermore, the examination of mitogen-activated protein kinase (MAPK) signaling status revealed that prolonged SFN treatment strongly up-regulated the extracellular-regulated kinase ½ (ERK1/2) in NCM460 but not HCT116 cells. Taken together, the activation of ERK1/2 in NCM460 but not HCT116 cells may play a critical role in SFN’s stronger potential of inhibiting colon cancer cell proliferation when compared with normal colon cells.