TY - JOUR
T1 - Induction of Apoptosis in Colorectal Carcinoma Cells Treated with 4-Hydroxy-2-nonenal and Structurally Related Aldehydic Products of Lipid Peroxidation
AU - West, James D.
AU - Ji, Chuan
AU - Duncan, Stephen T.
AU - Amarnath, Venkataraman
AU - Schneider, Claus
AU - Rizzo, Carmelo J.
AU - Brash, Alan R.
AU - Marnett, Lawrence J.
PY - 2004/4
Y1 - 2004/4
N2 - The oxidation of polyunsaturated fatty acids during oxidative stress gives rise to a series of toxic α,β-unsaturated aldehydes, including the electrophile 4-hydroxy-2-nonenal (4-HNE) and the related aldehydes, 4-hydroperoxy-2-nonenal (4-HPNE) and 4-oxo-2-nonenal (4-ONE). We synthesized these compounds, as well as the resolved enantiomers of 4-HNE, and compared their toxicities and apoptotic responses in the human colorectal cancer cell line RKO. All of these molecules execute similar death responses at comparable doses over almost identical time frames in RKO cells. The apoptotic response induced by 4-HPNE, 4-ONE, and 4-HNE enantiomers involves activation of caspases, proteolysis of downstream caspase targets, and nucleosomal DNA fragmentation. The results presented herein suggest that these molecules commonly activate certain signaling pathways that control cell death irrespective of their reactive properties.
AB - The oxidation of polyunsaturated fatty acids during oxidative stress gives rise to a series of toxic α,β-unsaturated aldehydes, including the electrophile 4-hydroxy-2-nonenal (4-HNE) and the related aldehydes, 4-hydroperoxy-2-nonenal (4-HPNE) and 4-oxo-2-nonenal (4-ONE). We synthesized these compounds, as well as the resolved enantiomers of 4-HNE, and compared their toxicities and apoptotic responses in the human colorectal cancer cell line RKO. All of these molecules execute similar death responses at comparable doses over almost identical time frames in RKO cells. The apoptotic response induced by 4-HPNE, 4-ONE, and 4-HNE enantiomers involves activation of caspases, proteolysis of downstream caspase targets, and nucleosomal DNA fragmentation. The results presented herein suggest that these molecules commonly activate certain signaling pathways that control cell death irrespective of their reactive properties.
UR - https://www.scopus.com/pages/publications/1942518353
UR - https://www.scopus.com/inward/citedby.url?scp=1942518353&partnerID=8YFLogxK
U2 - 10.1021/tx034248o
DO - 10.1021/tx034248o
M3 - Article
C2 - 15089087
AN - SCOPUS:1942518353
SN - 0893-228X
VL - 17
SP - 453
EP - 462
JO - Chemical Research in Toxicology
JF - Chemical Research in Toxicology
IS - 4
ER -