Lee Ju-Seog, Thorgeirsson Snorri S
Laboratory of Experimental Carcinogenesis, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Gastroenterology. 2004 Nov;127(5 Suppl 1):S51-5. doi: 10.1053/j.gastro.2004.09.015.
The heterogeneous nature of human hepatocellular carcinoma (HCC) has hampered both treatment and prognostic predictions. Gene expression profiles of human HCC were analyzed to define the molecular characteristics of the tumors and to test the prognostic value of the expression profiles. By applying global gene expression analyses, including unsupervised and supervised methods, 2 distinctive subclasses of HCC that were highly homogeneous for both the underlying biology and the clinical outcome were discovered. Tumors from the low survival subclass had strong cell proliferation and antiapoptosis gene expression signatures. In addition, the low survival subclass displayed higher expression of genes involved in ubiquitination and sumoylation, suggesting an etiologic involvement of these processes in accelerating the progression of HCC. Genes most strongly associated with survival were identified by using the Cox proportional hazards survival analysis. This approach identified a limited number of genes that accurately predicted the length of survival and provided new molecular insights into the pathogenesis of HCC. Future studies will evaluate potential diagnostic markers and therapeutic targets identified during the global gene expression studies. Furthermore, cross-species similarity of gene expression patterns will also allow prioritization of a long list of genes obtained from human gene expression profiling studies and focus on genes whose expression is altered during tumorigenesis in both species.
人类肝细胞癌(HCC)的异质性给治疗和预后预测带来了阻碍。对人类HCC的基因表达谱进行分析,以确定肿瘤的分子特征并检验表达谱的预后价值。通过应用包括无监督和有监督方法在内的全基因组表达分析,发现了HCC的2个独特亚类,它们在基础生物学和临床结果方面都高度同质。低生存亚类的肿瘤具有强烈的细胞增殖和抗凋亡基因表达特征。此外,低生存亚类显示出参与泛素化和类泛素化的基因表达较高,表明这些过程在加速HCC进展中存在病因学关联。通过使用Cox比例风险生存分析确定了与生存最密切相关的基因。这种方法确定了有限数量的能准确预测生存长度的基因,并为HCC的发病机制提供了新的分子见解。未来的研究将评估在全基因组表达研究中确定的潜在诊断标志物和治疗靶点。此外,基因表达模式的跨物种相似性也将使从人类基因表达谱研究中获得的一长串基因能够被优先排序,并聚焦于在两个物种肿瘤发生过程中表达发生改变的基因。