Oto Julia, Herranz Raquel, Verger Patricia, Roca Marta, Plana Emma, Miralles Manuel, Martínez-Sarmiento Manuel, Vera-Donoso César D, Medina Pilar
Haemostasis, Thrombosis, Arteriosclerosis and Vascular Biology Research Group, Medical Research Institute Hospital La Fe, Valencia, Spain.
Analytical Unit Platform, Medical Research Institute Hospital La Fe, Valencia, Spain.
J Proteomics. 2025 Jan 16;311:105357. doi: 10.1016/j.jprot.2024.105357. Epub 2024 Nov 17.
Renal cell carcinoma (RCC) stands among the most lethal urological malignancies. Most RCCs are incidentally diagnosed as initial symptoms are unspecific. Novel, minimally-invasive diagnostic and prognostic methods for RCC are needed, ideally in urine. Using UPLC-Q-ToF MS untargeted metabolomic analysis in urine, we previously revealed p-cresol glucuronide as potential RCC diagnostic marker. Additionally, urine samples one-year post-nephrectomy revealed isobutyryl-l-carnitine and L-proline betaine as potential RCC prognostic markers. Our present aim was to validate these differences in an independent cohort of RCC patients and healthy controls to strengthen their value as non-invasive biomarkers. In an independent cohort of 69 RCC patients and 52 controls we validated an increase in p-cresol glucuronide in urine from patients at diagnosis compared to controls (P = 0.0043). It remained increased one-year post-nephrectomy (P = 0.0288). The value of p-cresol glucuronide for RCC diagnosis was assessed with ROC curves analysis (AUC = 0.66, 95 % Confidence Interval 0.56-0.76). The role of isobutyryl-l-carnitine and L-proline betaine as prognostic markers could not be validated and will require a larger cohort. Our findings confirm the value of p-cresol glucuronide in urine as diagnostic marker for RCC in an independent cohort. This non-invasive method holds promise for enhancing patient care by reducing the need for potentially risky diagnostic procedures. Further metaproteomics-oriented approaches towards the tyrosine oxidation pathway and microbiota metagenomics studies may promote a holistic management of RCC. SIGNIFICANCE: Current imaging techniques available to diagnose and monitor renal cell carcinoma (RCC) are harmful for the patient given the high-radiation dose, and unspecific in low-grade tumors. Thus, novel non-invasive biomarkers with diagnostic and prognostic capabilities are of utmost importance. Herein, we have validated urine p-cresol glucuronide as diagnostic marker for RCC. This novel non-invasive biomarker could improve accurate assessments of tumor behavior, while enhancing patient outcomes by reducing discomfort and detrimental side effects.
肾细胞癌(RCC)是最致命的泌尿系统恶性肿瘤之一。大多数肾细胞癌是在偶然情况下被诊断出来的,因为其初始症状不具有特异性。因此,需要新的、微创的肾细胞癌诊断和预后评估方法,理想情况下是基于尿液检测的方法。我们之前通过超高效液相色谱-四极杆飞行时间质谱联用仪(UPLC-Q-ToF MS)对尿液进行非靶向代谢组学分析,发现对甲酚葡萄糖醛酸酯是潜在的肾细胞癌诊断标志物。此外,肾切除术后一年的尿液样本显示异丁酰-L-肉碱和L-脯氨酸甜菜碱是潜在的肾细胞癌预后标志物。我们目前的目标是在一个独立的肾细胞癌患者队列和健康对照中验证这些差异,以强化它们作为非侵入性生物标志物的价值。在一个由69名肾细胞癌患者和52名对照组成的独立队列中,我们验证了与对照组相比,肾细胞癌患者在诊断时尿液中对甲酚葡萄糖醛酸酯含量增加(P = 0.0043)。肾切除术后一年,该指标仍保持升高(P = 0.0288)。通过ROC曲线分析评估了对甲酚葡萄糖醛酸酯对肾细胞癌的诊断价值(AUC = 0.66,95%置信区间0.56 - 0.76)。异丁酰-L-肉碱和L-脯氨酸甜菜碱作为预后标志物的作用未能得到验证,这可能需要更大的队列研究。我们的研究结果证实了尿液中对甲酚葡萄糖醛酸酯作为肾细胞癌诊断标志物在独立队列中的价值。这种非侵入性方法有望通过减少对潜在高风险诊断程序的需求来改善患者护理。进一步针对酪氨酸氧化途径的元蛋白质组学方法和微生物群宏基因组学研究可能会促进肾细胞癌的整体管理。意义:目前用于诊断和监测肾细胞癌(RCC)的成像技术因辐射剂量高而对患者有害,并且在低级别肿瘤中不具有特异性。因此,具有诊断和预后能力的新型非侵入性生物标志物至关重要。在此,我们验证了尿液中的对甲酚葡萄糖醛酸酯作为肾细胞癌的诊断标志物。这种新型非侵入性生物标志物可以改善对肿瘤行为的准确评估,同时通过减少不适和有害副作用来提高患者的治疗效果。