| Literature DB >> 23758475 |
Nadège Rabiau1, Yann Dantal, Laurent Guy, Marjolaine Ngollo, Aslihan Dagdemir, Jean-Louis Kemeny, Benoît Terris, Annick Vieillefond, Jean-Paul Boiteux, Yves-Jean Bignon, Dominique Bernard-Gallon.
Abstract
In men at high risk for prostate cancer, established clinical and pathological parameters provide only limited prognostic information. Here we analyzed a French cohort of 103 prostate cancer patients and developed a gene panel model predictive of outcome in this group of patients. The model comprised of a 15-gene TaqMan Low-Density Array (TLDA) card, with gene expressions compared to a standardized reference. The RQ value for each gene was calculated, and a scoring system was developed. Summing all the binary scores (0 or 1) corresponding to the 15 genes, a global score is obtained between 0 and 15. This global score can be compared to Gleason score (0 to 10) by recalculating it into a 0-10 scaled score. A scaled score ≥2 suggested that the patient is suffering from a prostate cancer, and a scaled score ≥7 flagged aggressive cancer. Statistical analyses demonstrated a strongly significant linear correlation (p=3.50E-08) between scaled score and Gleason score for this prostate cancer cohort (N=103). These results support the capacity of this designed 15 target gene TLDA card approach to predict outcome in prostate cancer, opening up a new avenue for personalized medicine through future independent replication and applications for rapid identification of aggressive prostate cancer phenotypes for early intervention.Entities:
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Year: 2013 PMID: 23758475 PMCID: PMC3727569 DOI: 10.1089/omi.2012.0124
Source DB: PubMed Journal: OMICS ISSN: 1536-2310