Biroccio A, Benassi B, D'Agnano I, D'Angelo C, Buglioni S, Mottolese M, Ricciotti A, Citro G, Cosimelli M, Ramsay R G, Calabretta B, Zupi G
Experimental Chemotherapy Laboratory, Regina Elena Cancer Institute, Via delle Messi d'Oro 156, 00158, Rome, Italy.
Am J Pathol. 2001 Apr;158(4):1289-99. doi: 10.1016/S0002-9440(10)64080-1.
The aim of this study was twofold: to assess the relationship between c-Myb and Bcl-x expression and to evaluate the prognostic significance of their expression in colorectal carcinoma (CRC) patients. Analysis of tumors from 91 CRC patients for expression of c-Myb and Bcl-x revealed a significant relationship between these two proteins. Kaplan-Meier's analysis showed an increased risk of relapse and death in patients whose tumor specimens displayed high c-Myb levels and Bcl-x positivity. Similar results were also observed excluding Dukes' D patients. Molecular analysis using three c-Myb-overexpressing LoVo clones indicated that c-Myb overexpression was accompanied by up-regulation of Bcl-x(L) protein and mRNA. Tumors originating from these clones injected in nude mice were significantly larger than those formed in mice injected with parental or vector-transfected LoVo cells. Moreover, tumors derived from parental and control vector-transfected but not from c-Myb-overexpressing LoVo cells showed high frequency of apoptotic cells. These results provide direct evidence of an association between c-Myb and Bcl-x expression and suggest that expression of both molecules might be a useful prognostic marker in CRC.
评估c-Myb与Bcl-x表达之间的关系,并评估它们在结直肠癌(CRC)患者中的表达的预后意义。对91例CRC患者的肿瘤进行c-Myb和Bcl-x表达分析,发现这两种蛋白之间存在显著关系。Kaplan-Meier分析显示,肿瘤标本显示高c-Myb水平和Bcl-x阳性的患者复发和死亡风险增加。排除Dukes' D期患者后也观察到类似结果。使用三个过表达c-Myb的LoVo克隆进行分子分析表明,c-Myb过表达伴随着Bcl-x(L)蛋白和mRNA的上调。注射这些克隆来源肿瘤的裸鼠肿瘤明显大于注射亲本或载体转染的LoVo细胞的小鼠形成的肿瘤。此外,来自亲本和对照载体转染的肿瘤而非过表达c-Myb的LoVo细胞来源的肿瘤显示出高频率的凋亡细胞。这些结果提供了c-Myb与Bcl-x表达之间关联的直接证据,并表明这两种分子的表达可能是CRC中一个有用的预后标志物。