Cytoplasmic expression of CD133 sternness marker is associated with tumor aggressiveness in clear cell renal cell carcinoma

被引:12
|
作者
Zanjani, Leili Saeednejad [1 ]
Madjd, Zahra [1 ,2 ]
Abolhasani, Maryam [1 ,3 ]
Andersson, Yvonne [4 ]
Rasti, Arezoo [1 ]
Shariftabrizi, Ahmad [5 ]
Asgari, Mojgan [1 ,3 ]
机构
[1] IUMS, Oncopathol Res Ctr, Hemmat St Highway,Next Milad Tower, Tehran 1449614530, Iran
[2] Iran Univ Med Sci, Fac Adv Technol Med, Dept Mol Med, Tehran, Iran
[3] Iran Univ Med Sci, Hasheminejad Kidney Ctr, Tehran, Iran
[4] Oslo Univ Hosp, Norwegian Radium Hosp, Dept Tumor Biol, Oslo, Norway
[5] SUNY Buffalo, Dept Nucl Med & Mol Imaging, Buffalo, NY 14223 USA
关键词
CD133; Renal cell carcinoma (RCC); Cancer stem cells (CSCs); Tissue microarray (TMA); MICROSCOPIC VENOUS INVASION; CANCER STEM-CELLS; PROGENITOR CELLS; INTERNATIONAL-SOCIETY; PROGNOSTIC VALUE; PROGRESSION; PROMININ-1; PREDICTS;
D O I
10.1016/j.yexmp.2017.10.001
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Prominin-1 (CD133) is one of the most commonly used markers for cancer stem cells (CSCs), which are characterized by their ability for self-renewal and tumorigenicity. However, the clinical and prognostic significance of CSCs in renal cell carcinoma (RCC) remains unclear. The aim of this study was to investigate the expression patterns and prognostic significance of the cancer stem cell marker CD133 in different histological subtypes of RCC. CD133 expression was evaluated using immunohistochemistry in 193 well-defined renal tumor samples on tissue microarrays, including 136 (70.5%) clear cell renal cell carcinomas (CCRCCs), 26 (13.5%) papillary RCC5, and 31 (16.1%) chromophobe RCCs. The association between CD133 expression and clinicopathological features as well as the survival outcomes was determined. There was a statistically significant difference between CD133 expression among the different RCC subtypes. In CCRCC, higher cytoplasmic expression of CD133 was significantly associated with increase in grade, stage, microvascular invasion (MVI) and lymph node invasion (LNI), while no association was found with the membranous expression. Moreover, on multivariate analysis, TNM stage and nuclear grade were independent prognostic factors for overall survival (OS) in cytoplasmic expression. We showed that higher cytoplasmic CD133 expression was associated with more aggressive tumor behavior and more advanced disease in CCRCC but not in the other examined subtypes. Our results demonstrated that higher cytoplasmic CD133 expression is clinically significant in CCRCC and is associated with increased tumor aggressiveness and is useful for predicting cancer progression.
引用
收藏
页码:218 / 228
页数:11
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