Strategy for elucidating differentially expressed genes in leiomyomata identified by microarray technology

被引:47
作者
Catherino, WH
Prupas, C
Tsibris, JCM
Leppert, PC
Payson, M
Nieman, LK
Segars, JH
机构
[1] NICHD, Pediat & Reprod Endocrinol Branch, NIH, Bethesda, MD 20892 USA
[2] Combined Fed Program Reprod Endocrinol, Bethesda, MD USA
[3] Univ S Florida, Tampa, FL USA
关键词
fibroid; microarray; PCR; Dlk; Frizzled-2; CD-24;
D O I
10.1016/S0015-0282(03)00953-1
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: cDNA microarray technology identifies genes that are differentially expressed between tissues. Our previous study identified several genes that might contribute to the fibroid phenotype. We therefore sought to confirm genes involved in three distinct signal transduction pathways. Design: Evaluation of differential mRNA and protein expression of D1k, Frizzled-2, and CD-24 in fibroids compared with adjacent myometrium. Setting: University hospital. Patient(s): Five women undergoing medically indicated hysterectomy for symptomatic fibroids. Intervention(s): Microarray analysis of up to 33,000 genes, reverse transcriptase-polymerase chain reaction (RT-PCR), real-time RT-PCR, Western blot, and immunohistochemistry. Main Outcome Measure(s): Expression of mRNA transcripts and protein in fibroid compared with myometrium. Result(s): A more extensive microarray confirmed differential expression of Frizzled-2 and CD-24 but did not confirm Dlk overexpression. RT-PCR and real-time PCR demonstrated equivalent Dlk mRNA expression between fibroid and myometrium (ratio, 1.02), a slight Frizzled-2 overexpression (ratio, 2.09), and robust CD-24 overexpression in fibroids (ratio, 1-2.35). Western blot and immunohistochemistry confirmed Frizzled-2 overexpression, but did not confirm Dlk overexpression. Conclusion(s): Microarray technology is the first phase of tissue evaluation, but changes in gene expression must be confirmed. Confirmed genes can then be used to generate hypotheses testing their involvement in fibroid development. (C) 2003 by American Society for Reproductive Medicine.
引用
收藏
页码:282 / 290
页数:9
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