Biologic behavior of and p53 overexpression in multifocal renal cell carcinoma of clear cell type - An immunohistochemical study correlating grading,staging, and proliferation markers
A. Haitel et al., Biologic behavior of and p53 overexpression in multifocal renal cell carcinoma of clear cell type - An immunohistochemical study correlating grading,staging, and proliferation markers, CANCER, 85(7), 1999, pp. 1593-1598
BACKGROUND, In the treatment of small renal cell carcinoma (RCC), there is
controversy between radical and nephron-sparing surgical treatment because
of the risk of tumor multifocality. The biologic behavior of multifocal RCC
compared with that of unifocal RCC is not well investigated, and the relev
ance of p53 and the proliferation markers MIB-1 and proliferating cell nucl
ear antigen (PCNA) to multifocal RCC is not vet established.
METHODS. In this study, p53 protein overexpression was investigated immunoh
istochemically in 27 multifocal and GS unifocal clear cell RCCs using a mon
oclonal antibody (DO-1). The nuclear expression of p53 was compared with th
e expression of PCNA and MIB-1 (Ki-67 antigen) and other prognostic factors
, including grade and stage.
RESULTS. Thirty-three RCCs (35.9%) had p53 positive nuclear staining. MIB-1
positivity was significantly higher in p53 positive tumors than in p53 neg
ative turners. PCNA positivity was nor different in p53 positive tumors com
pared with p53 negative tumors. Proliferation marker expression was not ass
ociated with tumor focality. p53 overexpression was more often found in uni
focal tumors than in multifocal tumors. Intracellular accumulation of the p
53 protein was related to tumor grade bur not to the T classification of tu
mor stage. In addition, lymph node involvement was significantly associated
with p53 overexpression in tumors of the kidney. Focality did not influenc
e progression free survival.
CONCLUSIONS. This study demonstrated that there is no difference in the pro
liferative activity or biologic behavior of multifocal and unifocal tumors.
(C) 1999 American Cancer Society.