TY - JOUR
T1 - BPH gene expression profile associated to prostate gland volume
AU - Descazeaud, Aurelien
AU - Rubin, Mark A.
AU - Hofer, Matthias
AU - Setlur, Sunita
AU - Nikolaief, Nathalie
AU - Vacherot, Francis
AU - Soyeux, Pascale
AU - Kheuang, Laurence
AU - Abbou, Claude C.
AU - Allory, Yves
AU - De La Taille, Alexandre
PY - 2008/12
Y1 - 2008/12
N2 - 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 ot 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.
AB - 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 ot 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.
KW - Benign prostatic hyperplasia
KW - Gene expression
KW - Prostate volume
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U2 - 10.1097/PDM.0b013e31816f6352
DO - 10.1097/PDM.0b013e31816f6352
M3 - Article
C2 - 18936709
AN - SCOPUS:57649120002
SN - 1052-9551
VL - 17
SP - 207
EP - 213
JO - Diagnostic Molecular Pathology
JF - Diagnostic Molecular Pathology
IS - 4
ER -