Abstract

Backgrounds Clear cell renal cell carcinoma (ccRCC) is the most common histologic subtype of renal cell carcinoma (RCC) and shows a relatively poor prognosis among RCCs. Castor zinc finger 1 (CASZ1) is a transcription factor, prominently known for its tumor suppression role in neuroblastoma and other cancers. However, there has been no research about the prognostic significance of CASZ1 in ccRCC. In this study, we investigated CASZ1 expression in ccRCC and analyzed its prognostic implications. Methods A total of 896 ccRCC patients, who underwent surgical resection from 1995 to 2008, were included. We prepared tissue microarray blocks, evaluated CASZ1 nuclear expression by immunohistochemistry, and classified the cases into low or high expression categories. Results A low expression of CASZ1 was observed in 320 cases (35.7%) and was significantly associated with large tumor size, high World Health Organization/International Society of Urological Pathology (WHO/ISUP) grade, and high T category and M category. In survival analysis, a low expression of CASZ1 was significantly correlated with unfavorable progression-free survival (PFS) (p < 0.001), overall survival (OS) (p < 0.001), and cancer-specific survival (CSS) (p < 0.001) and was an independent prognostic factor for PFS and CSS in multivariate analysis adjusted for tumor size, WHO/ISUP grade, T category, N category, and M category. Conclusions Our study is the first to show the prognostic significance of CASZ1 expression in ccRCC. Our results revealed that low expression of CASZ1 is associated with poor prognosis and may serve as a new prognostic indicator.

Highlights

  • Kidney cancer is the 15th most common cancer and the 17th most common cause of cancer-related death worldwide [1]

  • Lymph node metastasis was found in 16 cases (1.8%), and distant metastasis was found in 68 cases (7.6%)

  • A high expression of Castor zinc finger 1 (CASZ1) was observed in 83.6% (749/896); a low expression of CASZ1 was observed in 16.4% (147/896)

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Summary

Introduction

Kidney cancer is the 15th most common cancer and the 17th most common cause of cancer-related death worldwide [1]. Renal cell carcinoma (RCC) is the most common malignant kidney tumor [2], and its incidence is increasing [3]. RCC is a heterogenous group of carcinomas that includes a clear cell subtype, a papillary subtype, and a chromophobe subtype [4]. Each subtype differs in histological characteristics, aggressiveness, and prognosis [5]. The most common histological subtype is the clear cell type, which makes up 80% of all RCCs [6]. For clear cell RCC (ccRCC), surgical excision is the primary treatment option, and in cases of surgically unresectable tumors or in cases of recurrence, pazopanib or sunitinib is used as first-line therapy [7]

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