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Serum circulating miRNA‐342‐3p as a potential diagnostic biomarker in parathyroid carcinomas: A pilot study
OBJECTIVE: To compare the serum miRNA expression profiles between patients with benign and malignant parathyroid tumours. BACKGROUND: Despite recent advances in molecular biology, a histological tissue biopsy is still the method of choice used to diagnose most cancers. The preoperative cytology is n...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502227/ https://www.ncbi.nlm.nih.gov/pubmed/34505413 http://dx.doi.org/10.1002/edm2.284 |
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author | Krupinova, Julia Mokrysheva, Natalya Petrov, Vasiliy Pigarova, Ekaterina Eremkina, Anna Dobreva, Ekaterina Ajnetdinova, Alina Melnichenko, Galina Tiulpakov, Anatoly |
author_facet | Krupinova, Julia Mokrysheva, Natalya Petrov, Vasiliy Pigarova, Ekaterina Eremkina, Anna Dobreva, Ekaterina Ajnetdinova, Alina Melnichenko, Galina Tiulpakov, Anatoly |
author_sort | Krupinova, Julia |
collection | PubMed |
description | OBJECTIVE: To compare the serum miRNA expression profiles between patients with benign and malignant parathyroid tumours. BACKGROUND: Despite recent advances in molecular biology, a histological tissue biopsy is still the method of choice used to diagnose most cancers. The preoperative cytology is not an applicable method for diagnosis of parathyroid cancer (PC); therefore, huge interest exists in terms of finding alternative methodologies to seek specific cancer biomarkers. DESIGN: A retrospective cross‐sectional study. PATIENTS AND METHODS: Serum samples of patients with PC (n = 13) and parathyroid adenoma (PA) (n = 11), age (p = .999) and sex (p = .999) were matched and examined via the simultaneous comparative expression analysis of 754 microRNAs (miRNAs). The «TaqMan OpenArray Human MicroRNA Panel» (Applied Biosystems) was used to conduct real‐time PCRs using the «QuantStudio 12К Flex» station (Life Technologies). RESULTS: According to the results of a pilot study, significant changes in expression levels between the PC group and the PA group (control) (p < .05) were observed for 17 miRNAs. Among them, the downregulation of miRNA‐342‐3p met the Benjamini‐Hochberg adjustment criteria for multiple comparisons (p = .02). CONCLUSIONS: Serum miRNA‐342‐3p could be a promising biomarker for PC to improve diagnosis and prognosis. |
format | Online Article Text |
id | pubmed-8502227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85022272021-10-14 Serum circulating miRNA‐342‐3p as a potential diagnostic biomarker in parathyroid carcinomas: A pilot study Krupinova, Julia Mokrysheva, Natalya Petrov, Vasiliy Pigarova, Ekaterina Eremkina, Anna Dobreva, Ekaterina Ajnetdinova, Alina Melnichenko, Galina Tiulpakov, Anatoly Endocrinol Diabetes Metab Original Research Articles OBJECTIVE: To compare the serum miRNA expression profiles between patients with benign and malignant parathyroid tumours. BACKGROUND: Despite recent advances in molecular biology, a histological tissue biopsy is still the method of choice used to diagnose most cancers. The preoperative cytology is not an applicable method for diagnosis of parathyroid cancer (PC); therefore, huge interest exists in terms of finding alternative methodologies to seek specific cancer biomarkers. DESIGN: A retrospective cross‐sectional study. PATIENTS AND METHODS: Serum samples of patients with PC (n = 13) and parathyroid adenoma (PA) (n = 11), age (p = .999) and sex (p = .999) were matched and examined via the simultaneous comparative expression analysis of 754 microRNAs (miRNAs). The «TaqMan OpenArray Human MicroRNA Panel» (Applied Biosystems) was used to conduct real‐time PCRs using the «QuantStudio 12К Flex» station (Life Technologies). RESULTS: According to the results of a pilot study, significant changes in expression levels between the PC group and the PA group (control) (p < .05) were observed for 17 miRNAs. Among them, the downregulation of miRNA‐342‐3p met the Benjamini‐Hochberg adjustment criteria for multiple comparisons (p = .02). CONCLUSIONS: Serum miRNA‐342‐3p could be a promising biomarker for PC to improve diagnosis and prognosis. John Wiley and Sons Inc. 2021-07-29 /pmc/articles/PMC8502227/ /pubmed/34505413 http://dx.doi.org/10.1002/edm2.284 Text en © 2021 The Authors. Endocrinology, Diabetes & Metabolism published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Articles Krupinova, Julia Mokrysheva, Natalya Petrov, Vasiliy Pigarova, Ekaterina Eremkina, Anna Dobreva, Ekaterina Ajnetdinova, Alina Melnichenko, Galina Tiulpakov, Anatoly Serum circulating miRNA‐342‐3p as a potential diagnostic biomarker in parathyroid carcinomas: A pilot study |
title | Serum circulating miRNA‐342‐3p as a potential diagnostic biomarker in parathyroid carcinomas: A pilot study |
title_full | Serum circulating miRNA‐342‐3p as a potential diagnostic biomarker in parathyroid carcinomas: A pilot study |
title_fullStr | Serum circulating miRNA‐342‐3p as a potential diagnostic biomarker in parathyroid carcinomas: A pilot study |
title_full_unstemmed | Serum circulating miRNA‐342‐3p as a potential diagnostic biomarker in parathyroid carcinomas: A pilot study |
title_short | Serum circulating miRNA‐342‐3p as a potential diagnostic biomarker in parathyroid carcinomas: A pilot study |
title_sort | serum circulating mirna‐342‐3p as a potential diagnostic biomarker in parathyroid carcinomas: a pilot study |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502227/ https://www.ncbi.nlm.nih.gov/pubmed/34505413 http://dx.doi.org/10.1002/edm2.284 |
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