miR-6805-5p as a biomarker of cisplatin-induced nephrotoxicity in patients with head and neck cancer

Torso, Nadine De Godoy; Quintanilha, Julia Coelho Franca; Cursino, Maria Aparecida; Pincinato, Eder De Carvalho; Loren, Pia; Salazar, Luis A.; Lima, Carmen Silvia Passos; Moriel, Patricia

Abstract

Introduction: The standard treatment for head and neck squamous cell carcinoma (HNSCC) is cisplatin chemoradiotherapy. One of the main treatment adverse reactions is nephrotoxicity, for which there is currently no adequate specific and sensitive biomarker. Thus, this study aimed to evaluate the use of microRNAs (miRNAs) as renal biomarker candidates.Methods: This was a retrospective cohort study. Nephrotoxicity was assessed through blood samples collected before and 5 days (D5) after chemotherapy. MiRNAs were extracted from urine samples collected at baseline and D5, and RNA sequencing identified miRNAs differentially expressed between participants with and without cisplatin-induced nephrotoxicity.Results: A total of 49 participants were included (n = 49). A significant difference was seen between the two groups for traditional renal markers (serum creatinine and creatinine clearance) and for the acute kidney injury (AKI) categories. Among the six miRNAs evaluated as biomarkers, four were upregulated (hsa-miR-6729-5p, hsa-miR-1238-5p, hsa-miR-4706, and hsa-miR-4322) and two were downregulated (hsa-miR-6805-5p and hsa-miR-21-5p), but only hsa-miR-6805-5p had a significant difference (p < 0.0001). Its receiver operating characteristic curve revealed excellent specificity (0.920) for its expression fluctuation assessment, while its absolute expression in D5 showed greater sensitivity (0.792).Conclusion: So, the integrated use of these two parameters seems to be an interesting approach for AKI.

Más información

Título según WOS: miR-6805-5p as a biomarker of cisplatin-induced nephrotoxicity in patients with head and neck cancer
Título de la Revista: FRONTIERS IN PHARMACOLOGY
Volumen: 14
Editorial: FRONTIERS MEDIA SA
Fecha de publicación: 2023
DOI:

10.3389/fphar.2023.1275238

Notas: ISI