OBJECTIVE: To determine the ability of p63 reactivity to confirm the diagnosis of urothelial carcinomas (UCs) that present clinically as kidney masses and to determine the association of p63 expression with clinicopathologic features in UCs. STUDY DESIGN: The study included 27 patients with renal pelvis UC and 42 patients with renal cell carcinoma (RCC). p63 Reactivity was examined immunohistochemically in tumor and nonneoplastic tissues. Correlation of p63 expression in renal malignancies (RCCs and UCs) was investigated and compared with clinicopathologic parameters. RESULTS: p63 Expression was detected in 25 of 27 (92.6%) UC cases while none of the RCC cases were positive for p63. There was a correlation between p63 expression and tumor stage, grade and survival time (p < 0.0001, = 0.032, = 0.028, respectively). However, no correlation was found between p63 expression and tumor progression (p = 0.513). CONCLUSION: p63 Should be considered as an additional biomarker to distinguish UC from RCC. Decreased p63 immunoreactivity was significantly associated with advanced tumor stage and grade. p63 Reactivity appears to be a useful prognostic factor in UC.
OBJECTIVE: To determine the ability of p63 reactivity to confirm the diagnosis of urothelial carcinomas (UCs) that present clinically as kidney masses and to determine the association of p63 expression with clinicopathologic features in UCs. STUDY DESIGN: The study included 27 patients with renal pelvis UC and 42 patients with renal cell carcinoma (RCC). p63 Reactivity was examined immunohistochemically in tumor and nonneoplastic tissues. Correlation of p63 expression in renal malignancies (RCCs and UCs) was investigated and compared with clinicopathologic parameters. RESULTS:p63 Expression was detected in 25 of 27 (92.6%) UC cases while none of the RCC cases were positive for p63. There was a correlation between p63 expression and tumor stage, grade and survival time (p < 0.0001, = 0.032, = 0.028, respectively). However, no correlation was found between p63 expression and tumor progression (p = 0.513). CONCLUSION:p63 Should be considered as an additional biomarker to distinguish UC from RCC. Decreased p63 immunoreactivity was significantly associated with advanced tumor stage and grade. p63 Reactivity appears to be a useful prognostic factor in UC.
Authors: Stefan Steurer; Claudia Riemann; Franziska Büscheck; Andreas M Luebke; Martina Kluth; Claudia Hube-Magg; Andrea Hinsch; Doris Höflmayer; Sören Weidemann; Christoph Fraune; Katharina Möller; Anne Menz; Margit Fisch; Michael Rink; Christian Bernreuther; Patrick Lebok; Till S Clauditz; Guido Sauter; Ria Uhlig; Waldemar Wilczak; David Dum; Ronald Simon; Sarah Minner; Eike Burandt; Rainer Krech; Till Krech; Andreas H Marx Journal: Biomark Res Date: 2021-01-25
Authors: Xiaohui Zhan; Yusong Liu; Christina Y Yu; Tian-Fu Wang; Jie Zhang; Dong Ni; Kun Huang Journal: BMC Med Genomics Date: 2020-12-28 Impact factor: 3.063