BRCA1, BRCA2, AR and IGF-I expression in prostate cancer: correlation between RT-qPCR and immunohistochemical detection |
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Authors: | Rabiau Nadège Déchelotte Pierre Adjakly Mawussi Kemeny Jean-Louis Guy Laurent Boiteux Jean-Paul Kwiatkowski Fabrice Bignon Yves-Jean Bernard-Gallon Dominique |
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Affiliation: | Centre Jean Perrin, Département d'Oncogénétique, EA 4233 Nutrition, Cancérogenèse et Thérapie Anti-tumorale, Centre Biomédical de Recherche et de Valorisation, 28 place Henri Dunant, B.P. 38, 63001 Clermont-Ferrand, France. |
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Abstract: | Identification and characterization of biomarkers in prostate cancer are important for improving the diagnosis. The aim of this study was to determine differences in the expression of 4 genes according to the stage of malignancy in prostate cancer. We analyzed BRCA1, BRCA2, androgen receptor (AR) and IGF-I gene expression in a cohort of 98 prostate biopsies. We used TaqMan RT-qPCR for mRNA detection, and correlation with proteins was performed using immunohistochemistry. Among the 98 studied prostate biopsies, high heterogeneity in the expression of the 4 genes was detected among the different histological types. However, down-regulation of BRCA1 and BRCA2 mRNA was detected, particularly in the normal tissues. The expression of AR was dependent on the stage of the tumor. The IGF-I gene was specifically expressed in the tumor tissues. Upon comparison between protein and mRNA expression for BRCA1, BRCA2 and AR, we obtained a trend; however, this did not achieve statistical significance. Regarding IGF-I, a correlation between mRNA expression and staining intensity of the protein was found to be significant (p<0.012). The AR biomarker was found to be slightly correlated with the prostate cancer diagnosis (p=0.013). AR was found to be decreased in the tumors with a 43% sensitivity and 90% specificity. The relative risk of 2.05 (1.13-3.69) indicated a 2?fold higher chance of cancer occurrence when AR was ≤0.206. |
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