S100A11 is a potential prognostic marker for clear cell renal cell carcinoma

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作者
Manal Gabril
Hala Girgis
Andreas Scorilas
Fabio Rotondo
Samantha Wala
Georg A. Bjarnason
Qiang Ding
Andrew Evans
Eriny Tawedrous
Maria Pasic
Antonio Finelli
Sahar Al-Haddad
George M. Yousef
机构
[1] Western University,Department of Pathology and Laboratory Medicine, London Health Sciences Centre
[2] St. Michael’s Hospital,Department of Laboratory Medicine and the Keenan Research Centre for Biomedical Science at the Li Ka Shing Knowledge Institute
[3] University of Toronto,Department of Laboratory Medicine and Pathobiology
[4] University of Athens,Division of Medical Oncology and Hematology
[5] Sunnybrook Odette Cancer Center,Department of Laboratory Medicine
[6] St. Joseph’s Health Centre,Division of Urologic Oncology, Department of Surgery, University Health Network, Princess Margaret Hospital
[7] University of Toronto,Department of Laboratory Medicine
[8] St. Michael’s Hospital,undefined
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关键词
S100A11; Prognosis; Renal cell carcinoma; Tumor markers; Metastasis; Molecular markers; Treatment;
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摘要
Clear cell renal cell carcinoma (ccRCC) is one of few cancers with rising incidence in North America. The prognosis of ccRCC is variable and difficult to predict. Stratification of patients according to disease aggressiveness can significantly improve patient management. We investigated the expression of the S100A11 protein in 385 patients with primary ccRCC using immunohistochemistry on tissue microarrays. We compared its expression with clinicopathologic parameters and patients’ survival. We also validated our results at the mRNA level on an independent set from The Cancer Genome Atlas. As a dichotomous variable (low vs. high expression), there was a significant association between S100A11 expression and tumor grade, with higher expression associated with higher tumor grades (p < 0.001). High expression was also significantly more frequently seen in higher versus lower stages (56 vs. 28 %). In the univariate analysis, high S100A11 expression was associated with significantly shorter disease-free survival (DFS) (HR = 2.28; p = 0.001). This was maintained in the multivariate analysis (HR = 1.69; p = 0.042). Expression was not associated with overall survival (OS) (p = 0.10). Comparable results were obtained when S100A11 expression was analyzed as a trichotomous variable (low, moderate, or high expression). The Kaplan–Meier survival analyses showed that higher S100A11 expression was associated with statistically significant decrease in DFS (p < 0.001), but not OS (p = 0.1).
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页码:63 / 71
页数:8
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