Prognostic Value of P63 Expression in Muscle-Invasive Bladder Cancer and Association with Molecular Subtypes-Preliminary Report

被引:0
|
作者
Sanguedolce, Francesca [1 ]
Falagario, Ugo Giovanni [2 ]
Zanelli, Magda [3 ]
Palicelli, Andrea [3 ]
Zizzo, Maurizio [4 ]
Ascani, Stefano [5 ]
Tortorella, Simona [1 ]
Busetto, Gian Maria [2 ]
Cormio, Angelo [6 ]
Carrieri, Giuseppe [2 ]
Cormio, Luigi [2 ,7 ]
机构
[1] Univ Foggia, Pathol Unit, Policlin Foggia, I-71122 Foggia, Italy
[2] Univ Foggia, Dept Urol & Renal Transplantat, Policlin Foggia, I-71122 Foggia, Italy
[3] Azienda USL IRCCS Reggio Emilia, Pathol Unit, I-42123 Reggio Emilia, Italy
[4] Azienda USL IRCCS Reggio Emilia, Surg Oncol Unit, I-42123 Reggio Emilia, Italy
[5] Univ Perugia, Pathol Unit, Azienda Osped Santa Maria di Terni, I-05100 Terni, Italy
[6] Univ Politecn Marche, Urol Unit, Azienda Osped Univ Osped Riuniti Di Ancona, I-60126 Ancona, Italy
[7] Bonomo Teaching Hosp, Dept Urol, I-76123 Andria, Italy
关键词
muscle-invasive bladder cancer; P63; prognosis; molecular subtyping; radical cystectomy; UROTHELIAL CARCINOMA; MARKERS;
D O I
10.3390/cimb46030155
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is an ongoing need for biomarkers that could reliably predict the outcome of BC and that could guide the management of this disease. In this setting, we aimed to explore the prognostic value of the transcription factor P63 in patients with muscle-invasive bladder cancer (MIBC) having undergone radical cystectomy. The correlation between P63 expression and clinicopathological features (tumor stage, nodes involvement, patterns of muscularis propria invasion, papillary architecture, anaplasia, concomitant carcinoma in situ, lymphovascular invasion, perineural invasion, necrosis) and molecular subtyping (basal and luminal type tumors) was tested in 65 radical cystectomy specimens and matched with cancer-specific survival (CSS) and overall survival (OS). P63-negative tumors displayed significantly higher rates of pattern 2 of muscularis propria invasion (50% vs. 14%, p = 0.002) and variant histology (45% vs. 19%, p = 0.022) compared to P63-positive ones. According to the combined expression of CK5/6 and CK20 (Algorithm #1), P63-positive and P63-negative tumors were mostly basal-like and double-negative, respectively (p = 0.004). Using Algorithm #2, based on the combined expression of CK5/6 and GATA3, the vast majority of tumors were luminal overall and in each group (p = 0.003). There was no significant difference in CSS and OS between P63-positive and P63-negative tumors, but the former featured a trend towards longer OS. Though associated with pathological features harboring negative prognostic potential, P63 status as such failed to predict CSS and OS. That said, it may contribute to better molecular subtyping of MIBC.
引用
收藏
页码:2456 / 2467
页数:12
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