Hung W C, Chaung L Y
School of Technology for Medical Sciences, Kaohsiung Medical College, No. 100, Shih-Chuan 1st Road, Kaohsiung 807, Taiwan, ROC.
Int J Oncol. 1998 Jan;12(1):137-40.
Deregulation in the ras oncogene is a common event in many types of human cancer. Our previous study clearly demonstrated that genetic alterations of ras oncogene are frequently found in human epithelial ovarian cancer. Recent reports have indicated that farnesyltransferase is involved in the regulation of post-translational modification and biological function of Ras proteins. Here, we report that a newly synthesized farnesyltransferase inhibitor, FPT inhibitor III, upregulates Bax and Bcl-xs expression and induces apoptosis in human ovarian cancer cells. This is a critical finding that farnesyltransferase inhibitors may directly activate apoptotic signaling pathways in cancer cells and may help to provide a new strategy in the treatment of human cancer.
Ras癌基因的失调在多种人类癌症中是常见事件。我们之前的研究清楚地表明,Ras癌基因的基因改变在人类上皮性卵巢癌中经常被发现。最近的报道指出,法尼基转移酶参与Ras蛋白的翻译后修饰和生物学功能的调节。在此,我们报告一种新合成的法尼基转移酶抑制剂,FPT抑制剂III,上调Bax和Bcl-xs的表达并诱导人卵巢癌细胞凋亡。这是一个关键发现,即法尼基转移酶抑制剂可能直接激活癌细胞中的凋亡信号通路,并可能有助于为人类癌症的治疗提供一种新策略。