Cancers (Aug 2021)

Urine LOX-1 and Volatilome as Promising Tools towards the Early Detection of Renal Cancer

  • Michela Murdocca,
  • Francesco Torino,
  • Sabina Pucci,
  • Manuela Costantini,
  • Rosamaria Capuano,
  • Chiara Greggi,
  • Chiara Polidoro,
  • Giuseppina Somma,
  • Valentina Pasqualetti,
  • Yolande Ketchanji Mougang,
  • Alexandro Catini,
  • Giuseppe Simone,
  • Roberto Paolesse,
  • Augusto Orlandi,
  • Alessandro Mauriello,
  • Mario Roselli,
  • Andrea Magrini,
  • Giuseppe Novelli,
  • Corrado Di Natale,
  • Federica Carla Sangiuolo

DOI
https://doi.org/10.3390/cancers13164213
Journal volume & issue
Vol. 13, no. 16
p. 4213

Abstract

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Renal cell carcinoma (RCC) represents around 3% of all cancers, within which clear cell RCC (ccRCC) are the most common type (70–75%). The RCC disease regularly progresses asymptomatically and upon presentation is recurrently metastatic, therefore, an early method of detection is necessary. The identification of one or more specific biomarkers measurable in biofluids (i.e., urine) by combined approaches could surely be appropriate for this kind of cancer, especially due to easy obtainability by noninvasive method. OLR1 is a metabolic gene that encodes for the Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), implicated in inflammation, atherosclerosis, ROS, and metabolic disorder-associated carcinogenesis. Specifically, LOX-1 is clearly involved in tumor insurgence and progression of different human cancers. This work reports for the first time the presence of LOX-1 protein in ccRCC urine and its peculiar distribution in tumoral tissues. The urine samples headspace has also been analyzed for the presence of the volatile compounds (VOCs) by SPME-GC/MS and gas sensor array. In particular, it was found by GC/MS analysis that 2-Cyclohexen-1-one,3-methyl-6-(1-methylethyl)- correlates with LOX-1 concentration in urine. The combined approach of VOCs analysis and protein quantification could lead to promising results in terms of diagnostic and prognostic potential for ccRCC tumors.

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