Manderson Emily N, Mes-Masson Anne-Marie, Novak Jaroslav, Lee Peter D, Provencher Diane, Hudson Thomas J, Tonin Patricia N
Department of Human Genetics, McGill University, Montreal, Quebec H3A 1B1, Canada.
Genome Res. 2002 Jan;12(1):112-21. doi: 10.1101/gr.174202.
We have investigated previously the utility of oligonucleotide expression microarray technology in an analysis of four spontaneously transformed epithelial ovarian cancer (EOC) cell lines, TOV-21G, TOV-81D, OV-90, and TOV-112D. Here, we examine the expression of 290 expressed sequence tags (ESTs) that map to human chromosome 3 in a primary culture derived from normal ovarian surface epithelium (NOSE), NOV-31, and the four spontaneously transformed EOC cell lines. One of these cell lines, OV-90, harbors a deletion of an entire chromosome 3p arm. Whereas the most aggressive cell lines (OV-90, TOV-112D, and TOV-21G) exhibited the highest levels of expression, assessed by the mean of expression values of all ESTs, OV-90 showed the lowest mean of expression of ESTs that map to the 3p arm in comparison with TOV-112D and TOV-21G. This difference in expression profile of 3p ESTs in OV-90 is also reflected in the ratio of expression of ESTs on 3p versus the 3q arm and in that the expression values of ESTs that map to 3p were more often lower than higher in OV-90 in two-way comparisons with NOV-31, TOV-21G, and TOV-112D. The loss of a 3p arm does not affect the pattern of differential expression in analyses based on the range of numeric expression values of each EST or fold differences in expression for each EST in comparison with NOV-31. However, 25 differentially expressed ESTs were identified on the basis of threefold differences in expression values between NOV-31 and any EOC cell line; and six of these ESTs were differentially expressed uniquely in OV-90. The investigation of these ESTs could facilitate the identification of novel chromosome 3 genes implicated in ovarian tumorigenesis.
我们之前研究了寡核苷酸表达微阵列技术在分析四种自发转化的上皮性卵巢癌(EOC)细胞系TOV-21G、TOV-81D、OV-90和TOV-112D中的效用。在此,我们检测了290个表达序列标签(EST)的表达情况,这些EST定位于来自正常卵巢表面上皮(NOSE)的原代培养物NOV-31以及这四种自发转化的EOC细胞系中的人类染色体3。其中一个细胞系OV-90缺失了整个3号染色体短臂。通过所有EST表达值的平均值评估,最具侵袭性的细胞系(OV-90、TOV-112D和TOV-21G)表现出最高的表达水平,而与TOV-112D和TOV-21G相比,OV-90中定位于3号染色体短臂的EST的平均表达水平最低。OV-90中3号染色体短臂EST表达谱的这种差异也反映在3号染色体短臂与3号染色体长臂EST的表达比例上,并且在与NOV-31、TOV-21G和TOV-112D的双向比较中,OV-90中定位于3号染色体短臂的EST的表达值更多时候是低于而非高于其他细胞系。在基于每个EST数值表达范围或与NOV-31相比每个EST表达倍数差异的分析中,3号染色体短臂的缺失并不影响差异表达模式。然而,基于NOV-31与任何EOC细胞系之间表达值三倍差异鉴定出了25个差异表达的EST;其中6个EST仅在OV-90中差异表达。对这些EST的研究可能有助于鉴定与卵巢肿瘤发生相关的新的3号染色体基因。