Comparison of microRNA profiles between benign and malignant salivary gland tumors in tissue, blood and saliva samples: a prospective, case-control study
- PMID: 27184509
- PMCID: PMC9444796
- DOI: 10.1016/j.bjorl.2016.03.013
Comparison of microRNA profiles between benign and malignant salivary gland tumors in tissue, blood and saliva samples: a prospective, case-control study
Abstract
Introduction: Salivary gland tumors (SGTs) are rare head and neck malignancies consisting of a spectrum of tumors with different biological behaviors.
Objective: In this study we aimed to find out differential expression of microRNA profiles between benign and malignant SGTs.
Methods: We investigated the possible role of 95 microRNAs in the 20 patients with salivary gland tumors with comparison of 17 patients without malignancy or salivary gland diseases. Sixteen of the tumors were benign (seven pleomorphic adenomas, nine Warthin tumors), four of them were malignant (two squamous cell carcinomas, one high grade mucoepidermoid carcinoma, one adenocarcinoma). Serum and saliva samples were collected from both patients and control group. Tissue samples of tumor masses were also collected from patient group.
Results: Among studied microRNAs miR-21, miR-23a, miR-27a, miR-223, miR-125b, miR-126, miR-146a, miR-30e were down regulated in the benign group compared to control group in the serum samples (p-values are 0.04, 0.00005, 0.00005, 0.0022, 0.031, 0.00008, 0.044, and 0.0007, respectively). When tissue samples were studied miR-21, miR-31, miR-199a-5p, miR-146b, miR-345 were up-regulated in the malignant group compared to benign group (p values are 0.006, 0.02, 0.013, 0.013, 0.041, respectively). miR-30e showed statistically significant up-regulation in malignant tumor group's plasma samples compared to benign group (p=0.034). There was no statistically significant difference in saliva samples between groups.
Conclusion: Our results showed that different microRNAs may play role in salivary tumor pathogenesis according to biological behavior. Although there was no difference in saliva samples between groups, according to tissue and serum samples miR-21 and 30e may have an important role; since they were down-regulated in benign tumors whereas up-regulated in malignant ones.
Introdução: Os tumores da glândula salivar (TGS) são lesões malignas raras de cabeça e pescoço que consistem em um espectro de tumores com diferentes comportamentos biológicos.
Objetivo: Neste estudo, tivemos como objetivo identificar a expressão diferencial de perfis de microRNA entre TGS benignos e malignos.
Método: Investigamos a possível participação de 95 microRNA em 20 pacientes com tumores de glândulas salivares comparado a 17 pacientes sem doença maligna ou doenças das glândulas salivares; 16 dos tumores eram benignos (sete adenomas pleomórficos, nove tumores de Warthin), quatro deles eram malignos (dois carcinomas espinocelulares, carcinoma mucoepidermoide de alto grau, um adenocarcinoma). As amostras de soro e saliva foram coletadas de pacientes e do grupo controle. Amostras de tecido dos tumores também foram colhidas do grupo de pacientes com tumores.
Resultados: Entre os microRNA estudados, miR-21, miR-23a, miR-27a, miR-223, miR-125b, miR-126, miR-146a, miR-30e foram infrarregulados no grupo benigno em comparação com o grupo controle nas amostras do soro (os valores de p são 0,04, 0,00005, 0,00005, 0,0022, 0,031, 0,00008, 0,044 e 0,0007, respectivamente). Quando as amostras de tecido foram estudadas, miR-21, o miR-31, o miR-199-5p, miR-146b, o miR-345 foram suprarregulados no grupo maligno em relação ao grupo benigno (valores de p são 0,006, 0,02, 0,013, 0,013, 0,041, respectivamente). O miR-30e apresentou suprarregulação estatisticamente significativa em amostras de plasma do grupo de tumor maligno em relação ao grupo benigno (p = 0,034). Não houve diferença estatisticamente significativa em amostras de saliva entre os grupos.
Conclusão: Nossos resultados mostraram que diferentes microRNA podem desempenhar um papel na patogenia do tumor salivar de acordo com o comportamento biológico. Embora não tenha havido diferença em amostras de saliva entre os grupos, de acordo com as amostras de tecido e de soro, miR-21 e 30e podem ter um papel importante, já que foram infrarregulados nos tumores benignos enquanto suprarregulados nos tumores malignos.
Keywords: MicroRNA; Pathogenesis; Patogenia; Salivary gland tumor; Tumor de glândula salivar; miR-21; miR-30e.
Copyright © 2016 Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial. Published by Elsevier Editora Ltda. All rights reserved.
Figures
Similar articles
-
A microRNA signature for the differential diagnosis of salivary gland tumors.PLoS One. 2019 Jan 25;14(1):e0210968. doi: 10.1371/journal.pone.0210968. eCollection 2019. PLoS One. 2019. PMID: 30682201 Free PMC article.
-
MiR-26a and miR-191 are upregulated while PLAG1 and HIF2 are downregulated in pleomorphic adenomas of the salivary glands compared to Warthin tumors.J Oral Pathol Med. 2024 Aug;53(7):451-457. doi: 10.1111/jop.13565. Epub 2024 Jun 9. J Oral Pathol Med. 2024. PMID: 38853518
-
Altered expression of apoptosis-regulating miRNAs in salivary gland tumors suggests their involvement in salivary gland tumorigenesis.Virchows Arch. 2017 Mar;470(3):291-299. doi: 10.1007/s00428-016-2049-z. Epub 2016 Dec 15. Virchows Arch. 2017. PMID: 27981346
-
A systematic review on the role of biomarkers in liquid biopsies and saliva samples in the monitoring of salivary gland cancer.Acta Otolaryngol. 2023 Aug;143(8):709-713. doi: 10.1080/00016489.2023.2238757. Epub 2023 Aug 3. Acta Otolaryngol. 2023. PMID: 37534452 Review.
-
2021 Update on Diagnostic Markers and Translocation in Salivary Gland Tumors.Int J Mol Sci. 2021 Jun 24;22(13):6771. doi: 10.3390/ijms22136771. Int J Mol Sci. 2021. PMID: 34202474 Free PMC article. Review.
Cited by
-
Prognostic impact of MUC1 and potential regulatory miR-145 and miR-21 expression in salivary mucoepidermoid carcinoma.Head Neck Pathol. 2022 Dec;16(4):1134-1145. doi: 10.1007/s12105-022-01475-0. Epub 2022 Aug 18. Head Neck Pathol. 2022. PMID: 35980523 Free PMC article.
-
Circulating microRNAs in head and neck cancer: a scoping review of methods.Clin Exp Metastasis. 2019 Jun;36(3):291-302. doi: 10.1007/s10585-019-09961-6. Epub 2019 Mar 14. Clin Exp Metastasis. 2019. PMID: 30877500 Review.
-
Circulating miR-31 as an effective biomarker for detection and prognosis of human cancer: a meta-analysis.Oncotarget. 2017 Apr 25;8(17):28660-28671. doi: 10.18632/oncotarget.15638. Oncotarget. 2017. PMID: 28404921 Free PMC article.
-
A microRNA signature for the differential diagnosis of salivary gland tumors.PLoS One. 2019 Jan 25;14(1):e0210968. doi: 10.1371/journal.pone.0210968. eCollection 2019. PLoS One. 2019. PMID: 30682201 Free PMC article.
-
Differentially Expressed MiRNAs of Goat Submandibular Glands Among Three Developmental Stages Are Involved in Immune Functions.Front Genet. 2021 Jun 15;12:678194. doi: 10.3389/fgene.2021.678194. eCollection 2021. Front Genet. 2021. PMID: 34211501 Free PMC article.
References
-
- Eveson J.W., Auclair P.L., Gnepp D.R., El-Naggar A.K. In: World Health Organization classifications of tumours: pathology & genetics. Head and neck tumours. Barnes E.L., Eveson J.W., Reichart P., Sidransky D., editors. IARC Press; Lyon: 2005. Tumors of the salivary glands: introduction; pp. 221–222.
-
- Speight P.M., Barrett A.W. Salivary gland tumours. Oral Dis. 2002;8:229–240. - PubMed
-
- Muscat J.E., Wynder E.L. A case/control study of risk factors for major salivary gland cancer. Otolaryngol Head Neck Surg. 1998;118:195–198. - PubMed
-
- He Q., Zhou X., Li S., Jin Y., Chen Z., Chen D., et al. MicroRNA-181a suppresses salivary adenoid cystic carcinoma metastasis by targeting MAPK-Snai2 pathway. Biochim Biophys Acta. 2013;1830:5258–5266. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical