微阵列的显著性分析
增生
前列腺
基因
基因表达
前列腺切除术
前列腺癌
DNA微阵列
前列腺特异性抗原
PCA3系列
基因表达谱
医学
泌尿科
癌症研究
生物
内科学
癌症
遗传学
作者
A. Descazeaud,Mark A. Rubin,Matthias D. Hofer,Sunita R. Setlur,Nathalie Nikolaief,Francis Vacherot,Pascale Soyeux,Laurence Kheuang,C.C. Abbou,Yves Allory,Alexandre de la Taille
出处
期刊:Diagnostic Molecular Pathology
[Ovid Technologies (Wolters Kluwer)]
日期:2008-11-19
卷期号:17 (4): 207-213
被引量:24
标识
DOI:10.1097/pdm.0b013e31816f6352
摘要
The aim of the current study was to analyze gene expression profiles in benign prostatic hyperplasia and to compare them with phenotypic properties. Thirty-seven specimens of benign prostatic hyperplasia were obtained from symptomatic patients undergoing surgery. RNA was extracted and hybridized to Affymetrix Chips containing 54,000 gene expression probes. Gene expression profiles were analyzed using cluster, TreeView, and significance analysis of microarrays softwares. In an initial unsupervised analysis, our 37 samples clustered hierarchically in 2 groups of 18 and 19 samples, respectively. Five clinical parameters were statistically different between the 2 groups: in group 1 compared with group 2, patients had larger prostate glands, had higher prostate specific antigen levels, were more likely to be treated by α blockers, to be operated by prostatectomy, and to have major irritative symptoms. The sole independent parameter associated with this dichotome clustering, however, was the prostate gland volume. Therefore, the role of prostate volume was explored in a supervised analysis. Gene expression of prostate glands <60 mL and >60 mL were compared using significance analysis of microarrays and 227 genes were found differentially expressed between the 2 groups (>2 change and false discovery rate of <5%). Several specific pathways including growth factors genes, cell cycle genes, apoptose genes, inflammation genes, and androgen regulated genes, displayed major differences between small and large prostate glands.
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