TY - JOUR
T1 - Different bile acids exhibit distinct biological effects
T2 - The tumor promoter deoxycholic acid induces apoptosis and the chemopreventive agent ursodeoxycholic acid inhibits cell proliferation
AU - Martinez, Jesse D.
AU - Stratagoules, Elias D.
AU - LaRue, Janna M.
AU - Powell, Ashley A.
AU - Gause, Paul R.
AU - Craven, Mary T.
AU - Payne, Claire M.
AU - Powell, Marianne B.
AU - Gerner, Eugene W.
AU - Earnest, David L.
N1 - Funding Information:
The authors thank Norma Seaver for expert technical assistance in operation of the Becton Dickinson FACScan flow cytometer and subsequent analysis of the data. This work was supported by National Institutes of Health Grants P01-CA-72008 (to E. W. Gerner and J. D. Martinez) and ES-06694 (to C. M. Payne) and Cancer Center Core Grant CA-23074 (to Arizona Cancer Center) and by Arizona Disease Control Research Commission Grants 9621 and 9524 (to C. M. Payne). E. D. Stratagoules and J. M. LaRue were supported, in part, by Howard Hughes Medical Institute Grant 71195-521303 (to the Undergraduate Biological Research Program at the University of Arizona). Address reprint requests to Jesse Martinez, The University of Arizona, Dept. of Radiation Oncology, 1501 N. Campbell Ave., PO Box 245024, Tucson, AZ 85724. Phone: (520) 626-4250. FAX: (520) 626-4480. Email: JMARTINEZ@AZCC.ARIZONA.EDU.
PY - 1998
Y1 - 1998
N2 - Epidemiological studies have suggested that the concentration and composition of fecal bile acids are important determining factors in the etiology of colon cancer. However, the mechanism by which these compounds influence tumor development is not understood. To begin to elucidate their mechanism of action, four bile acids, cholic acid, chenodeoxycholic acid, deoxycholic acid (DCA), and ursodeoxycholic acid, were examined for their effects on the growth of several different tumor cell lines. We found that incubating cells with chenodeoxycholic acid or DCA caused morphological changes, seen by electron and light microscopy, that were characteristic of apoptosis, whereas incubating cells with ursodeoxycholic acid inhibited cell proliferation but did not induce apoptosis. Cholic acid had no discernible effect on cells. Notably, the apoptosis induced by DCA could be suppressed by inhibiting protein kinase C activity with calphostin C. These results indicate that different bile acids exhibit distinct biological activities and suggest that the cytotoxicity reported for DCA may be due to its capacity to induce apoptosis via a protein kinase C-dependent signaling pathway.
AB - Epidemiological studies have suggested that the concentration and composition of fecal bile acids are important determining factors in the etiology of colon cancer. However, the mechanism by which these compounds influence tumor development is not understood. To begin to elucidate their mechanism of action, four bile acids, cholic acid, chenodeoxycholic acid, deoxycholic acid (DCA), and ursodeoxycholic acid, were examined for their effects on the growth of several different tumor cell lines. We found that incubating cells with chenodeoxycholic acid or DCA caused morphological changes, seen by electron and light microscopy, that were characteristic of apoptosis, whereas incubating cells with ursodeoxycholic acid inhibited cell proliferation but did not induce apoptosis. Cholic acid had no discernible effect on cells. Notably, the apoptosis induced by DCA could be suppressed by inhibiting protein kinase C activity with calphostin C. These results indicate that different bile acids exhibit distinct biological activities and suggest that the cytotoxicity reported for DCA may be due to its capacity to induce apoptosis via a protein kinase C-dependent signaling pathway.
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U2 - 10.1080/01635589809514689
DO - 10.1080/01635589809514689
M3 - Article
C2 - 9770722
AN - SCOPUS:0031751777
VL - 31
SP - 111
EP - 118
JO - Nutrition and Cancer
JF - Nutrition and Cancer
SN - 0163-5581
IS - 2
ER -