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Molecular characterization of low grade and high grade bladder cancer

BACKGROUND: Bladder cancer (BC) is the 9(th) most common cancer diagnosis worldwide. Low grade (LG) represents 70% of all BCs, characterized by recurrence and rare ability (10–15%) to progress to high grade (HG) and invade. The remaining 30% is high grade (HG), fast invasive BC, which is resistant t...

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Detalles Bibliográficos
Autores principales: Apollo, Alessandro, Ortenzi, Valerio, Scatena, Cristian, Zavaglia, Katia, Aretini, Paolo, Lessi, Francesca, Franceschi, Sara, Tomei, Sara, Sepich, Carlo Alberto, Viacava, Paolo, Mazzanti, Chiara Maria, Naccarato, Antonio Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334926/
https://www.ncbi.nlm.nih.gov/pubmed/30650148
http://dx.doi.org/10.1371/journal.pone.0210635
Descripción
Sumario:BACKGROUND: Bladder cancer (BC) is the 9(th) most common cancer diagnosis worldwide. Low grade (LG) represents 70% of all BCs, characterized by recurrence and rare ability (10–15%) to progress to high grade (HG) and invade. The remaining 30% is high grade (HG), fast invasive BC, which is resistant to therapy. Identifying biomarkers for predicting those tumors able to progress is a key goal for patient outcome improvement. This study focuses on the most promising prognostic markers. MATERIALS AND METHODS: TP53 and FGFR3 mutational status, Survivin, CK19, CK20, E-cadherin and CD44 gene expression analysis were performed on 66 BCs. RESULTS: Survivin was found associated to tumor grade (p<0.05). Moreover, Survivin correlated with CD44 in TP53 wild type (p = 0.0242) and FGFR3 wild type (p = 0.0036) tumors. In particular the Survivin-CD44 correlation was associated to HG FGFR3 wild type BCs (p = 0.0045). Unsupervised hierarchical clustering based on gene expression data identified four distinct molecular groups reflecting the patient histology (p = 0.038). CONCLUSION: We suggest Survivin, both as a biomarker associated to G3 BCs but negatively related to TP53 mutational status, and as a potential novel therapeutic target.