Cheng Timothy C, Manorek Gerald, Samimi Goli, Lin Xinjian, Berry Charles C, Howell Stephen B
Department of Medicine, The University of California Medical Center, La Jolla, San Diego, 92093-0819, USA.
Cancer Chemother Pharmacol. 2006 Sep;58(3):384-95. doi: 10.1007/s00280-005-0171-8. Epub 2006 Jan 11.
The goal of this study was to identify genes consistently differentially expressed in multiple pairs of isogenic cisplatin (DDP)-sensitive and resistant human ovarian carcinoma cell lines using microarray-based expression profiling. Expression profiling was carried out on six pairs of ovarian carcinoma cells lines growing under identical conditions; each cell expression profile was independently replicated six times. No genes were differentially expressed in all six pairs of cells or even in even in any five of the six pairs. Eighteen genes and 1 EST were upregulated, and four genes and 1 EST were downregulated, in at least four cell pairs. Of these, only metallothionein 2A has previously been implicated in DDP resistance. Among the genes identified on the basis of six replicates, an average of 24.8% would have been missed if only five replicates had been performed, and 38.3% would have been missed with only four replicates. The genes did not identify a dominant biochemical pathway or ontology category as being linked to DDP resistance; however, hierarchical clustering provided evidence for two classes DDP-resistant phenotypes within which there are additional cell pair-specific alterations. Many of the genes identified in this study play important roles in cell surface interactions and trafficking pathways not previously linked to DDP resistance. The genes discovered by this extensively replicated analysis are candidates for prediction of DDP responsiveness in ovarian cancer patients.
本研究的目的是利用基于微阵列的表达谱分析,鉴定在多对同基因顺铂(DDP)敏感和耐药的人卵巢癌细胞系中持续差异表达的基因。对在相同条件下生长的六对卵巢癌细胞系进行了表达谱分析;每个细胞表达谱独立重复六次。在所有六对细胞中甚至在六对中的任何五对中都没有发现差异表达的基因。在至少四对细胞中,有18个基因和1个EST上调,4个基因和1个EST下调。其中,只有金属硫蛋白2A先前被认为与DDP耐药有关。在基于六次重复鉴定出的基因中,如果只进行五次重复,平均会遗漏24.8%的基因,如果只进行四次重复,则会遗漏38.3%的基因。这些基因未确定与DDP耐药相关的主要生化途径或本体类别;然而,层次聚类为两种DDP耐药表型提供了证据,在这两种表型中存在额外的细胞对特异性改变。本研究中鉴定出的许多基因在以前与DDP耐药无关的细胞表面相互作用和运输途径中发挥重要作用。通过这种广泛重复分析发现的基因是预测卵巢癌患者DDP反应性的候选基因。