TY - JOUR
T1 - Enzyme induction and cytotoxicity of phenethyl isothiocyanate and its glutathione conjugate towards breast cancer cells
AU - Lam, Yui Sze
AU - Owusu-Apenten, Richard
PY - 2013
Y1 - 2013
N2 - Chemoprevention using isothiocyanates is partly the result of the induction ofphase II enzymes for carcinogen detoxification from healthy cells. However,phase II enzyme activity can impair cancer therapeutic agents. The objective ofthis study was to assess phase II enzyme induction and cytotoxicity of phenethylisothiocyanate (PEITC) and glutathione conjugate with PEITC (GsPEITC) usingMCF-7 and MDA-MB-231 breast cancer cells. Changes of phase II enzymes,glutathione-S-transferase (GST) and NAD(P)H quinone reductase (QR), weremeasured by colorimetric procedures. Cell viability was determined using theMTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-di-phenyltetrazolium- bromide) assay.From current results, 24hr exposure to 50 μM) of PEITC or GsPEITC increased phase IIenzyme activity by a maximum of 500-700-percent. To conclude, cytotoxic dosesof PEITC or GsPEITC possess phase II enzyme inducing activity in MCF-7 andMDA-MB-231 breast cancer cells.
AB - Chemoprevention using isothiocyanates is partly the result of the induction ofphase II enzymes for carcinogen detoxification from healthy cells. However,phase II enzyme activity can impair cancer therapeutic agents. The objective ofthis study was to assess phase II enzyme induction and cytotoxicity of phenethylisothiocyanate (PEITC) and glutathione conjugate with PEITC (GsPEITC) usingMCF-7 and MDA-MB-231 breast cancer cells. Changes of phase II enzymes,glutathione-S-transferase (GST) and NAD(P)H quinone reductase (QR), weremeasured by colorimetric procedures. Cell viability was determined using theMTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-di-phenyltetrazolium- bromide) assay.From current results, 24hr exposure to 50 μM) of PEITC or GsPEITC increased phase IIenzyme activity by a maximum of 500-700-percent. To conclude, cytotoxic dosesof PEITC or GsPEITC possess phase II enzyme inducing activity in MCF-7 andMDA-MB-231 breast cancer cells.
U2 - 10.12988/pacs.2013.3514
DO - 10.12988/pacs.2013.3514
M3 - Article
SN - 1314-7633
VL - 1
SP - 63
EP - 73
JO - Pure and Applied Chemical Sciences
JF - Pure and Applied Chemical Sciences
IS - 2
ER -