TY - JOUR
T1 - Plasma miR-151-3p as a Candidate Diagnostic Biomarker for Head and Neck Cancer
T2 - A Cross-sectional Study within the INHANCE Consortium
AU - Pastorino, Roberta
AU - Sassano, Michele
AU - Tiziano, Francesco Danilo
AU - Giraldi, Luca
AU - Amore, Rosarita
AU - Arzani, Dario
AU - Abiusi, Emanuela
AU - Ahrens, Wolfgang
AU - Vilches, Laia Alemany
AU - Canova, Cristina
AU - Healy, Claire Mary
AU - Holcatova, Ivana
AU - Lagiou, Pagona
AU - Polesel, Jerry
AU - Popovic, Maja
AU - Nygård, Ståle
AU - Cadoni, Gabriella
AU - Znaor, Ariana
AU - Boffetta, Paolo
AU - Matsuo, Keitaro
AU - Oze, Isao
AU - Brennan, Paul
AU - Boccia, Stefania
N1 - Publisher Copyright:
© 2022 The Authors.
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Background: Identification of screening tests for the detection of head and neck cancer (HNC) at an early stage is an important strategy to improving prognosis. Our objective was to identify plasma circulating miRNAs for the diagnosis of HNC (oral and laryngeal subsites), within a multicenter International Head and Neck Cancer Epidemiology consortium. Methods: A high-throughput screening phase with 754 miRNAs was performed in plasma samples of 88 cases and 88 controls, followed by a validation phase of the differentially expressed miRNAs, identified in the screening, in samples of 396 cases and 396 controls. Comparison of the fold changes (FC) was carried out using the Wilcoxon rank-sum test and the Dunn multiple comparison test. Results: We identified miR-151-3p (FC = 1.73, P = 0.007) as differentially expressed miRNAs in the screening and validation phase. The miR-151-3p was the only overexpressed miRNA in validation sample of patients with HNC with early stage at diagnosis (FC = 1.81, P = 0.008) and it was confirmed upregulated both in smoker early-stage cases (FC = 3.52, P = 0.024) and in nonsmoker early-stage cases (FC = 1.60, P = 0.025) compared with controls. Conclusions: We identified miR-151-3p as an early marker of HNC. This miRNA was the only upregulated in patients at early stages of the disease, independently of the smoking status. Impact: The prognosis for HNC is still poor. The discovery of a new diagnostic biomarker could lead to an earlier tumor discovery and therefore to an improvement in patient prognosis.
AB - Background: Identification of screening tests for the detection of head and neck cancer (HNC) at an early stage is an important strategy to improving prognosis. Our objective was to identify plasma circulating miRNAs for the diagnosis of HNC (oral and laryngeal subsites), within a multicenter International Head and Neck Cancer Epidemiology consortium. Methods: A high-throughput screening phase with 754 miRNAs was performed in plasma samples of 88 cases and 88 controls, followed by a validation phase of the differentially expressed miRNAs, identified in the screening, in samples of 396 cases and 396 controls. Comparison of the fold changes (FC) was carried out using the Wilcoxon rank-sum test and the Dunn multiple comparison test. Results: We identified miR-151-3p (FC = 1.73, P = 0.007) as differentially expressed miRNAs in the screening and validation phase. The miR-151-3p was the only overexpressed miRNA in validation sample of patients with HNC with early stage at diagnosis (FC = 1.81, P = 0.008) and it was confirmed upregulated both in smoker early-stage cases (FC = 3.52, P = 0.024) and in nonsmoker early-stage cases (FC = 1.60, P = 0.025) compared with controls. Conclusions: We identified miR-151-3p as an early marker of HNC. This miRNA was the only upregulated in patients at early stages of the disease, independently of the smoking status. Impact: The prognosis for HNC is still poor. The discovery of a new diagnostic biomarker could lead to an earlier tumor discovery and therefore to an improvement in patient prognosis.
UR - https://www.scopus.com/pages/publications/85143379744
U2 - 10.1158/1055-9965.EPI-22-0376
DO - 10.1158/1055-9965.EPI-22-0376
M3 - Article
C2 - 36126276
AN - SCOPUS:85143379744
SN - 1055-9965
VL - 31
SP - 2237
EP - 2243
JO - Cancer Epidemiology Biomarkers and Prevention
JF - Cancer Epidemiology Biomarkers and Prevention
IS - 12
ER -