Different bile acids exhibit distinct biological effects: The tumor promoter deoxycholic acid induces apoptosis and the chemopreventive agent ursodeoxycholic acid inhibits cell proliferation

被引:183
作者
Martinez, JD
Stratagoules, ED
LaRue, JM
Powell, AA
Gause, PR
Craven, MT
Payne, CM
Powell, MB
Gerner, EW
Earnest, DL
机构
[1] Univ Arizona, Dept Radiat Oncol, Tucson, AZ 85724 USA
[2] Univ Arizona, Arizona Canc Ctr, Tucson, AZ 85724 USA
[3] Univ Arizona, Dept Med, Tucson, AZ 85724 USA
[4] Univ Arizona, Dept Immunol & Microbiol, Arizona Res Labs, Tucson, AZ 85724 USA
来源
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL | 1998年 / 31卷 / 02期
关键词
D O I
10.1080/01635589809514689
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 nor 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 ifs capacity to induce apoptosis via a protein kinase C-dependent signaling pathway.
引用
收藏
页码:111 / 118
页数:8
相关论文
共 40 条
[1]   ENVIRONMENTAL FACTORS AND CANCER INCIDENCE AND MORTALITY IN DIFFERENT COUNTRIES, WITH SPECIAL REFERENCE TO DIETARY PRACTICES [J].
ARMSTRONG, B ;
DOLL, R .
INTERNATIONAL JOURNAL OF CANCER, 1975, 15 (04) :617-631
[2]   UNCONJUGATED SECONDARY BILE-ACIDS IN THE SERUM OF PATIENTS WITH COLORECTAL ADENOMAS [J].
BAYERDORFFER, E ;
MANNES, GA ;
OCHSENKUHN, T ;
DIRSCHEDL, P ;
WIEBECKE, B ;
PAUMGARTNER, G .
GUT, 1995, 36 (02) :268-273
[3]  
BEDI A, 1995, CANCER RES, V55, P1811
[4]   REGULATION OF PROTEIN-KINASE-C AND ROLE IN CANCER BIOLOGY [J].
BLOBE, GC ;
OBEID, LM ;
HANNUN, YA .
CANCER AND METASTASIS REVIEWS, 1994, 13 (3-4) :411-431
[5]  
BRATTAIN MG, 1981, CANCER RES, V41, P1751
[6]  
CLEMENS MJ, 1992, J CELL SCI, V103, P881
[7]  
COHEN BI, 1980, J NATL CANCER I, V64, P573
[8]  
CRAVEN PA, 1986, CANCER RES, V46, P5754
[9]   ROLE OF ACTIVATION OF PROTEIN-KINASE-C IN THE STIMULATION OF COLONIC EPITHELIAL PROLIFERATION AND REACTIVE OXYGEN FORMATION BY BILE-ACIDS [J].
CRAVEN, PA ;
PFANSTIEL, J ;
DERUBERTIS, FR .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (02) :532-541
[10]  
EARNEST DL, 1994, CANCER RES, V54, P5071