Decreased ARID1A expression correlates with poor prognosis of clear cell renal cell carcinoma

被引:31
|
作者
Park, Jeong Hwan [1 ]
Lee, Cheot [1 ]
Suh, Ja Hee [1 ]
Chae, Ji Yoen [1 ]
Kim, Hwal Woong [2 ]
Moon, Kyung Chul [1 ,3 ]
机构
[1] Seoul Natl Univ Coll Med, Dept Pathol, Seoul 110799, South Korea
[2] Good Moonhwa Hosp, Dept Pathol, Pusan 601803, South Korea
[3] Seoul Natl Univ Coll Med, Kidney Res Inst, Med Res Ctr, Seoul 110799, South Korea
基金
新加坡国家研究基金会;
关键词
ARID1A; Clear cell renal cell carcinoma; Progression; Prognosis; Immunohistochemistry; SWI/SNF-RELATED COMPLEXES; GENE; CANCER;
D O I
10.1016/j.humpath.2014.12.002
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Clear cell renal cell carcinoma (CCRCC) is the most common renal cell carcinoma. It has a relatively unfavorable prognosis compared to other common renal cell carcinomas. Recently, comprehensive molecular studies in CCRCC revealed important genetic alterations, including changes in the VHL, PBRM1, and ARID1A genes. The expression of ARID1A protein is associated with tumor progression and prognosis in many cancers. This study aimed to evaluate the nuclear expression of ARID1A in CCRCC and to assess its expression with the clinical prognosis. The nuclear expression of ARID1A was evaluated in 290 cases of CCRCC by immunohistochemistry. To determine the clinicopathological association with ARID1A, each of the cases was divided into 2 groups, low- and high-expression groups, according to the average proportion of nuclear staining. Decreased ARID1A expression was associated with the higher nuclear grade and higher pTNM stage (P < .001 and P = .013, respectively). The ARID 1 A low-expression group revealed significantly shorter cancer-specific and progression-free survival times (P = .001 and P < .001, respectively). Furthermore, Cox regression analysis showed that ARID1A expression was an independent prognostic factor for progression-free survival (P = .009). These results suggest that nuclear expression of ARID1A may serve as a new prognostic marker in CCRCC patients. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:454 / 460
页数:7
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