Martinez J D, Stratagoules E D, LaRue J M, Powell A A, Gause P R, Craven M T, Payne C M, Powell M B, Gerner E W, Earnest D L
Department of Radiation Oncology, Arizona Cancer Center, Tucson 85724, USA.
Nutr Cancer. 1998;31(2):111-8. doi: 10.1080/01635589809514689.
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.
流行病学研究表明,粪便胆汁酸的浓度和组成是结肠癌病因的重要决定因素。然而,这些化合物影响肿瘤发展的机制尚不清楚。为了开始阐明它们的作用机制,研究了四种胆汁酸,即胆酸、鹅去氧胆酸、脱氧胆酸(DCA)和熊去氧胆酸,观察它们对几种不同肿瘤细胞系生长的影响。我们发现,用鹅去氧胆酸或DCA孵育细胞会导致形态学变化,通过电子显微镜和光学显微镜观察到这些变化是凋亡的特征,而用熊去氧胆酸孵育细胞会抑制细胞增殖,但不会诱导凋亡。胆酸对细胞没有明显影响。值得注意的是,用钙泊三醇抑制蛋白激酶C活性可以抑制DCA诱导的凋亡。这些结果表明不同的胆汁酸表现出不同的生物学活性,并提示所报道的DCA的细胞毒性可能是由于其通过蛋白激酶C依赖的信号通路诱导凋亡的能力。