Integrative Genomic Analyses Reveal an Androgen-Driven Somatic Alteration Landscape in Early-Onset Prostate Cancer
Menée sur des échantillons tumoraux prélevés sur 18 patients atteints d'un cancer de la prostate (11 patients jeunes, 8 patients âgés), cette étude met en évidence des différences dans les réarrangements structuraux du génome tumoral en fonction de l'âge des patients au diagnostic
Early-onset prostate cancer (EO-PCA) represents the earliest clinical manifestation of prostate cancer. To compare the genomic alteration landscapes of EO-PCA with classical (elderly-onset) PCA, we performed deep sequencing-based genomics analyses in 11 tumors diagnosed at young age, and pursued comparative assessments with seven elderly-onset PCA genomes. Remarkable age-related differences in structural rearrangement (SR) formation became evident, suggesting distinct disease pathomechanisms. Whereas EO-PCAs harbored a prevalence of balanced SRs, with a specific abundance of androgen-regulated ETS gene fusions including TMPRSS2:ERG, elderly-onset PCAs displayed primarily non-androgen-associated SRs. Data from a validation cohort of > 10,000 patients showed age-dependent androgen receptor levels and a prevalence of SRs affecting androgen-regulated genes, further substantiating the activity of a characteristic androgen-type pathomechanism in EO-PCA.
º Genome sequencing revealed age-related genetic alterations in PCA
º Early-onset PCAs display a specific abundance of androgen-driven rearrangements
º These age-linked alterations coincide with activity levels of the androgen receptor
º This is an observation of age-specific DNA alterations in a common cancer
Cancer cell , résumé, 2012