Cheng Xiaodong, Young Travis W, Mei Fang C
Department of Pharmacology and Toxicology, Sealy Center for Cancer Cell Biology, The University of Texas Medical Branch, Galveston, Texas 77555-1031, USA.
Front Biosci. 2007 Sep 1;12:5166-74. doi: 10.2741/2556.
Using a genetically defined human ovarian cancer model, we have analyzed the protein expression profile of human ovarian cancer cells established by oncogenic RAS transformation. Cells were immortalized by retroviral transfection of SV40 t/T antigens and the catalytic subunit of telomerase (hTERT). Careful analyses of protein targets associated with oncogenic transformation have enabled us to identify several novel signaling pathways that play important roles in oncogenic transformation of human ovarian epithelial cells.
利用一个基因定义的人类卵巢癌模型,我们分析了通过致癌性RAS转化建立的人类卵巢癌细胞的蛋白质表达谱。通过逆转录病毒转染SV40 t/T抗原和端粒酶催化亚基(hTERT)使细胞永生化。对与致癌性转化相关的蛋白质靶点进行仔细分析,使我们能够识别出在人类卵巢上皮细胞致癌性转化中起重要作用的几个新的信号通路。