Circulating MicroRNAs in Patients with Vulvar Squamous Cell Carcinoma and Its Precursors

<b>Objectives</b>: Vulvar squamous cell carcinoma (VSCC) is a rare gynecologic malignancy, with most cases arising from differentiated vulvar intraepithelial neoplasia (dVIN). Approximately one-third of VSCC cases originate from high-grade squamous intraepithelial lesions (HSILs), which...

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Main Authors: Julia Rymuza, Angelika Długosz, Kamil Zalewski, Artur Kowalik, Mateusz Bujko, Magdalena Kowalewska
Format: Article
Language:English
Published: MDPI AG 2025-02-01
Series:Non-Coding RNA
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Online Access:https://www.mdpi.com/2311-553X/11/1/13
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author Julia Rymuza
Angelika Długosz
Kamil Zalewski
Artur Kowalik
Mateusz Bujko
Magdalena Kowalewska
author_facet Julia Rymuza
Angelika Długosz
Kamil Zalewski
Artur Kowalik
Mateusz Bujko
Magdalena Kowalewska
author_sort Julia Rymuza
collection DOAJ
description <b>Objectives</b>: Vulvar squamous cell carcinoma (VSCC) is a rare gynecologic malignancy, with most cases arising from differentiated vulvar intraepithelial neoplasia (dVIN). Approximately one-third of VSCC cases originate from high-grade squamous intraepithelial lesions (HSILs), which are associated with persistent infection by varieties of high-risk human papillomavirus (hrHPV). This study aimed to quantify the circulating microRNAs (miRNAs) in the plasma of patients with premalignant conditions (dVIN and HSILs) and VSCC using TaqMan Low-Density Arrays. <b>Methods</b>: Plasma samples were collected from 40 patients, including those treated for HSILs, dVIN, and VSCC. Quantitative real-time PCR (qRT-PCR) identified the circulating miRNAs differentially expressed in the plasma of VSCC patients compared to patients with precancerous lesions. <b>Results</b>: A total of 31 differentially expressed miRNAs (DEMs) were found to be significantly upregulated in plasma from VSCC patients compared to precancerous cases. None of the analyzed miRNAs were able to distinguish VSCC cases based on hrHPV tumor status. <b>Conclusions</b>: This study provides strong evidence that a distinct set of miRNAs can differentiate between plasma samples from VSCC patients and those with precancerous lesions. Thus, these DEMs have potential diagnostic and prognostic value. “Predisposing” DEMs could be developed as biomarkers to aid in the assessment of vulvar lesions, helping to exclude or confirm progression toward cancer.
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spelling doaj-art-c41f2104f12b4fbea6e396e904d144d82025-08-20T02:01:24ZengMDPI AGNon-Coding RNA2311-553X2025-02-011111310.3390/ncrna11010013Circulating MicroRNAs in Patients with Vulvar Squamous Cell Carcinoma and Its PrecursorsJulia Rymuza0Angelika Długosz1Kamil Zalewski2Artur Kowalik3Mateusz Bujko4Magdalena Kowalewska5Department of Molecular and Translational Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, PolandDepartment of Immunology, Biochemistry and Nutrition, Medical University of Warsaw, 02-091 Warsaw, PolandDepartment of Molecular and Translational Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, PolandDepartment of Molecular Diagnostics, Holycross Cancer Centre, 25-734 Kielce, PolandDepartment of Molecular and Translational Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, PolandDepartment of Molecular and Translational Oncology, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, Poland<b>Objectives</b>: Vulvar squamous cell carcinoma (VSCC) is a rare gynecologic malignancy, with most cases arising from differentiated vulvar intraepithelial neoplasia (dVIN). Approximately one-third of VSCC cases originate from high-grade squamous intraepithelial lesions (HSILs), which are associated with persistent infection by varieties of high-risk human papillomavirus (hrHPV). This study aimed to quantify the circulating microRNAs (miRNAs) in the plasma of patients with premalignant conditions (dVIN and HSILs) and VSCC using TaqMan Low-Density Arrays. <b>Methods</b>: Plasma samples were collected from 40 patients, including those treated for HSILs, dVIN, and VSCC. Quantitative real-time PCR (qRT-PCR) identified the circulating miRNAs differentially expressed in the plasma of VSCC patients compared to patients with precancerous lesions. <b>Results</b>: A total of 31 differentially expressed miRNAs (DEMs) were found to be significantly upregulated in plasma from VSCC patients compared to precancerous cases. None of the analyzed miRNAs were able to distinguish VSCC cases based on hrHPV tumor status. <b>Conclusions</b>: This study provides strong evidence that a distinct set of miRNAs can differentiate between plasma samples from VSCC patients and those with precancerous lesions. Thus, these DEMs have potential diagnostic and prognostic value. “Predisposing” DEMs could be developed as biomarkers to aid in the assessment of vulvar lesions, helping to exclude or confirm progression toward cancer.https://www.mdpi.com/2311-553X/11/1/13vulvar squamous cell carcinomavulvar intraepithelial neoplasiavulvar high-grade squamous intraepithelial lesionscirculating microRNAmiR-145miR-221
spellingShingle Julia Rymuza
Angelika Długosz
Kamil Zalewski
Artur Kowalik
Mateusz Bujko
Magdalena Kowalewska
Circulating MicroRNAs in Patients with Vulvar Squamous Cell Carcinoma and Its Precursors
Non-Coding RNA
vulvar squamous cell carcinoma
vulvar intraepithelial neoplasia
vulvar high-grade squamous intraepithelial lesions
circulating microRNA
miR-145
miR-221
title Circulating MicroRNAs in Patients with Vulvar Squamous Cell Carcinoma and Its Precursors
title_full Circulating MicroRNAs in Patients with Vulvar Squamous Cell Carcinoma and Its Precursors
title_fullStr Circulating MicroRNAs in Patients with Vulvar Squamous Cell Carcinoma and Its Precursors
title_full_unstemmed Circulating MicroRNAs in Patients with Vulvar Squamous Cell Carcinoma and Its Precursors
title_short Circulating MicroRNAs in Patients with Vulvar Squamous Cell Carcinoma and Its Precursors
title_sort circulating micrornas in patients with vulvar squamous cell carcinoma and its precursors
topic vulvar squamous cell carcinoma
vulvar intraepithelial neoplasia
vulvar high-grade squamous intraepithelial lesions
circulating microRNA
miR-145
miR-221
url https://www.mdpi.com/2311-553X/11/1/13
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