Yuan Bao-Zhu, Zhou Xiaoling, Zimonjic Drazen B, Durkin Marian E, Popescu Nicholas C
Laboratory of Experimental Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland 20892-4258, USA.
J Mol Diagn. 2003 Feb;5(1):48-53. doi: 10.1016/S1525-1578(10)60451-5.
DNA amplification in cancer cells frequently involves oncogenes whose increased expression confers a selective advantage on tumor cell growth. In an attempt to identify novel oncogenes involved in hepatocarcinogenesis, representational difference analysis (RDA) was performed using DNA from a primary human hepatocellular carcinoma (HCC) that showed high-level DNA amplifications on chromosomes 1p32 and 11q13 by comparative genomic hybridization. Ten amplification fragments were isolated by RDA, and when used to probe Southern blots of tumor DNA, there was a 5- to 50-fold increase in hybridization intensity relative to normal DNA. The sequence of one amplification product matched that of the EMS1 oncogene, which is located on chromosome 11q13 and is amplified in other cancers. We detected EMS1 amplification in 3 of 17 primary HCC. Overexpression of EMS1 mRNA was observed in 12 of 14 HCC cell lines in the absence of gene amplification or an increased copy-number of the gene. The EMS1 gene encodes cortactin, a cortical actin-associated protein that is a substrate for Src kinase and is involved in cytoskeleton organization. Alterations of the EMS1 gene that lead to overexpression of cortactin may be associated with tumor development in HCC. EMS1 amplification and overexpresion is indicative of unfavorable prognosis in several cancers and may have similar prognostic implications in liver cancer.
癌细胞中的DNA扩增常常涉及癌基因,其表达增加赋予肿瘤细胞生长以选择性优势。为了鉴定参与肝癌发生的新癌基因,利用来自原发性人类肝细胞癌(HCC)的DNA进行了代表性差异分析(RDA),通过比较基因组杂交显示该肿瘤在染色体1p32和11q13上有高水平的DNA扩增。通过RDA分离出10个扩增片段,当用于探测肿瘤DNA的Southern印迹时,相对于正常DNA,杂交强度增加了5至50倍。其中一个扩增产物的序列与EMS1癌基因的序列匹配,EMS1位于染色体11q13上,在其他癌症中也有扩增。我们在17例原发性HCC中的3例中检测到EMS1扩增。在14株HCC细胞系中的12株中观察到EMS1 mRNA的过表达,且不存在基因扩增或基因拷贝数增加的情况。EMS1基因编码cortactin,一种与皮质肌动蛋白相关的蛋白,它是Src激酶的底物,参与细胞骨架组织。导致cortactin过表达的EMS1基因改变可能与HCC的肿瘤发生有关。EMS1扩增和过表达在几种癌症中提示预后不良,在肝癌中可能也有类似的预后意义。