Abstract

ABSTRACTPurposeto determine the usefulness of serum TF as a potential marker for patients with clear cell RCC.Materials and Methodsprospective study of 30 patients with clear cell RCC submitted to nephrectomy and 16 controls without clear cell RCC treated surgically for other conditions. TF is a endothelium marker that was correlated with worse prognosis in a variety of solid tumors including RCC. Serum TF was collected before surgery at the operating room and in the postoperative setting after at least four weeks. Serum samples were analyzed with a commercial ELISA kit for human TF (R&D Systems®).ResultsMean preoperative serum TF levels in clear cell RCC patients and in controls were 66.8 pg/dL and 28.4 pg/dL, respectively (p<0.001). Mean postoperative serum TF levels in clear cell RCC patients were 26.3 pg/dL. In all patients with clear cell RCC postoperative serum levels of TF were lower, with a mean reduction of 41.6 pg/dL in the postoperative setting (p<0.001). Linear regression revealed that tumor size was correlated with the postoperative reduction of serum TF levels (p=0.037).ConclusionsWe have shown a 3-fold reduction in the median preoperative serum levels of TF in patients with clear cell RCC after surgery. We have also shown a difference of the same magnitude in the serum levels of TF compared with those of a control group of patients with benign diseases. TF appears to be a useful serum marker for the presence of clear cell RCC. Further studies are needed to validate these findings.

Highlights

  • Clear cell renal cell carcinoma (RCC) corresponds to 85% of all renal malignancies, with an estimated 66.000 new cases in the U.S in 2016 [1]

  • The present study aims to determine whether serum levels of Tissue factor (TF) are useful as biomarkers in clear cell RCC

  • We have shown for the first time that in the preoperative setting, patients with clear cell RCC have serum TF levels three times higher than those of patients with other diseases

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Summary

Introduction

Clear cell renal cell carcinoma (RCC) corresponds to 85% of all renal malignancies, with an estimated 66.000 new cases in the U.S in 2016 [1]. In 2012, there were about 142.000 deaths due to kidney neoplasms, representing the 16th most common cause of cancer specific mortality [2]. Mortality rates of renal malignancies have increased in underdeveloped and in developing countries in recent years [4]. The search for new diagnostic and prognostic biomarkers in clear cell RCC has evolved slowly over the years. The most frequently mutated were: PBRM1, that is part of the chromatin remodeling complex, BAP1 and SETd2, which are hisibju | Tissue factor as a biomarker in kidney cancer tones relevant to this process [14, 15]. No serum biomarker has proven clinically useful in clear cell RCC

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