Microarray analysis of gene expression mirrors the biology of an ovarian cancer model

被引:62
作者
Tonin, PN
Hudson, TJ
Rodier, F
Bossolasco, M
Lee, PD
Novak, J
Manderson, EN
Provencher, D
Mes-Masson, AM
机构
[1] McGill Univ, Dept Med, Montreal, PQ H3G 1A4, Canada
[2] McGill Univ, Dept Human Genet, Montreal, PQ H3A 1B1, Canada
[3] McGill Univ, Ctr Hlth, Res Inst, Montreal, PQ H3G 1A4, Canada
[4] McGill Univ, Ctr Hlth, Montreal Genome Ctr, Montreal, PQ H3G 1A4, Canada
[5] MIT, Whitehead Inst Biomed Res, Ctr Genome Res, Cambridge, MA 02139 USA
[6] Univ Montreal, Ctr Hosp, Ctr Rech, Hop Notre Dame, Montreal, PQ H2L 4M1, Canada
[7] Univ Montreal, Inst Canc Montreal, Montreal, PQ H2L 4M1, Canada
[8] Univ Montreal, Dept Obstet Gynecol, Montreal, PQ H3C 3J7, Canada
[9] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
基金
英国医学研究理事会;
关键词
epithelial ovarian cancer; cell model; high-density microarray analysis; RNA expression analysis; signature patterns;
D O I
10.1038/sj.onc.1204804
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have previously described an ovarian cancer model based on four independent spontaneously immortalized epithelial ovarian cancer cell lines (TOV-21G, TOV-81D, TOV-112D and OV-90) from patients who were never exposed to chemotherapy or radiation therapy. These cell lines are particularly interesting since they retain characteristics of the original epithelial ovarian cancers (EOC) from which they were derived. Here we report the characterization of this model system using high-density DNA microarrays in order to assess gene expression. Expression profiles were generated from total RNAs extracted from the four EOC cell lines. For comparison, expression profiling is also provided for a primary culture of normal ovarian surface epithelium (NOV-31) and a fresh EOC sample (TOV-578G). Comparison of expression profiles revealed patterns of expression that distinguish NOV-31 from that of all tumor derived samples. The expression pattern of Tov-81D, an EOC cell line that was derived from a patient with indolent disease, most closely resembles NOV-31 while profiles of samples derived from patients with more aggressive disease (TOV-21G, OV-90, TOV-112D and TOV-578G) showed more divergent patterns of expression. The microarray analysis (http://genome.mcgill.ca) results confirm the usefulness of an ovarian cancer model based on the characterization of these EOC cell lines.
引用
收藏
页码:6617 / 6626
页数:10
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