Potential Role of Selected miRNAs in the Pathogenesis of Autoimmune Thyroid Diseases in Children and Adolescents.

Beata Sawicka, Anetta Sulewska, Agnieszka Kulczy��ska-Przybik, Filip Bossowski, Maciej Dulewicz, Hanna Borysewicz-Sa��czyk, Barbara Mroczko, Jacek Nikli��ski, Artur Bossowski
Author Information
  1. Beata Sawicka: Department of Pediatrics, Endocrinology, Diabetology, with Cardiology Divisions, Medical University of Bialystok, 15-089 Bialystok, Poland.
  2. Anetta Sulewska: Department of Clinical Molecular Biology, Medical University of Bialystok, 15-089 Bialystok, Poland. ORCID
  3. Agnieszka Kulczy��ska-Przybik: Department of Neurodegeneration Diagnostics, Medical University of Bialystok, 15-089 Bialystok, Poland.
  4. Filip Bossowski: Department of Pediatrics, Endocrinology, Diabetology, with Cardiology Divisions, Medical University of Bialystok, 15-089 Bialystok, Poland. ORCID
  5. Maciej Dulewicz: Department of Neurodegeneration Diagnostics, Medical University of Bialystok, 15-089 Bialystok, Poland. ORCID
  6. Hanna Borysewicz-Sa��czyk: Department of Pediatrics, Endocrinology, Diabetology, with Cardiology Divisions, Medical University of Bialystok, 15-089 Bialystok, Poland.
  7. Barbara Mroczko: Department of Neurodegeneration Diagnostics, Medical University of Bialystok, 15-089 Bialystok, Poland. ORCID
  8. Jacek Nikli��ski: Department of Clinical Molecular Biology, Medical University of Bialystok, 15-089 Bialystok, Poland.
  9. Artur Bossowski: Department of Pediatrics, Endocrinology, Diabetology, with Cardiology Divisions, Medical University of Bialystok, 15-089 Bialystok, Poland. ORCID

Abstract

BACKGROUND: Many epigenetic factors, including microRNAs, are involved in the process of changing gene expressions. Small non-coding RNA molecules, called miRNAs, are responsible for regulating gene translation by silencing or degrading target mRNAs. It is acknowledged that for many diseases, they may be novel diagnostic and prognostic biomarkers. Patients with autoimmune thyroid diseases are more likely to develop nodules in the thyroid tissue, and Hashimoto's thyroiditis and Graves' disease predispose patients to thyroid cancer. We evaluated the concentrations of microRNA molecules (miR-15a-5p, miR-126-3p, miR-142-5p, miR-21-5p, miR-150-5p) in the blood of children with thyroid disorders. In addition, we wished to identify molecules whose change in concentration predisposes to the development of thyroid cancer.
AIM: The aim of this study is to evaluate selected epigenetic elements by analyzing the levels of miR-15a-5p, miR-126-3p, miR-142-5p, miR-150-5p and miR-21-5p in the blood of pediatric patients with Graves' disease ( = 25), Hashimoto's thyroiditis ( = 26) and thyroid nodular disease ( = 20) compared to a control group of healthy children ( = 17).
MATERIALS AND METHODS: The study consists of groups of children and adolescents aged 10-18 years with autoimmune thyroid disease, with thyroid nodular disease compared to a control group. The miR-15a-5p, miR-126-3p, miR-142-5p, miR-21-5p and miR-150-5p molecules were determined through an immunoenzymatic assay using BioVendor reagents.
RESULTS: There is a statistically significant decrease in the expression of the miR-15a-5p in children with Graves' disease (21.61 vs. 50.22 amol/��L, = 0.03) and in patients with thyroid nodular disease compared to controls (20.23 vs. 50.22 amol/��L, = 0.04). Higher levels of the miR-142-5p molecule are found in patients with thyroid disease (with GD-3.8 vs. 3.14 amol/��L, = 0.01; with HT-3.7 vs. 3.14 amol/��L, = NS, with thyroid nodular disease-4.16 vs. 3.14 amol/��L, = 0.04). Lower levels of miR-126-3p were noted in the GD group compared to the control group (7.09 vs. 7.24 amol/��L, = 0.02). No statistically significant changes in the expressions of miR-150-5p and miR-21-5p molecules were observed in the study groups.
CONCLUSIONS: 1. The overexpression of the miR-142-5p molecule occurs in children and adolescents with thyroid diseases. 2. Decreased blood levels of miR-15a-5p predispose patients to the formation of focal lesions in the thyroid gland. 3. Identifying a lower expression of the miR-126-3p molecule in the blood of children with GD requires careful follow-up for the development of focal lesions in the thyroid gland and evaluation for their potential malignancy.

Keywords

References

  1. Children (Basel). 2022 Jul 23;9(8): [PMID: 35892612]
  2. Front Biosci (Landmark Ed). 2022 Mar 16;27(3):101 [PMID: 35345333]
  3. Thyroid. 2018 Mar;28(3):319-327 [PMID: 29378472]
  4. Int J Pediatr Otorhinolaryngol. 2023 Feb;165:111425 [PMID: 36696711]
  5. Clin Chim Acta. 2020 Sep;508:77-91 [PMID: 32407782]
  6. Stat Med. 2009 Mar 30;28(7):1159-75 [PMID: 19170020]
  7. Cancers (Basel). 2022 Jun 23;14(13): [PMID: 35804851]
  8. Int J Mol Sci. 2023 Feb 05;24(4): [PMID: 36834570]
  9. Mol Carcinog. 2022 Mar;61(3):301-310 [PMID: 34727409]
  10. Onco Targets Ther. 2019 Aug 06;12:6217-6226 [PMID: 31496725]
  11. Mol Immunol. 2022 Jan;141:21-32 [PMID: 34785326]
  12. J Clin Med. 2022 Mar 23;11(7): [PMID: 35407376]
  13. Thyroid. 2022 Sep;32(9):1109-1117 [PMID: 35950619]
  14. PLoS One. 2015 Aug 05;10(8):e0130496 [PMID: 26244545]
  15. J Transl Med. 2016 Jun 08;14(1):166 [PMID: 27277258]
  16. Crit Rev Eukaryot Gene Expr. 2022;32(6):1-10 [PMID: 35997113]
  17. Oncol Lett. 2022 Feb;23(2):67 [PMID: 35069876]
  18. Thyroid. 2016 Oct;26(10):1450-1456 [PMID: 27541075]
  19. Cells. 2022 Aug 31;11(17): [PMID: 36078129]
  20. Genetics. 1964 Jan;49(1):49-67 [PMID: 17248194]
  21. J Transl Med. 2021 Mar 6;19(1):99 [PMID: 33676540]
  22. Eur J Endocrinol. 2015 Dec;173(6):801-8 [PMID: 26374873]
  23. Endocr Relat Cancer. 2019 May;26(5):525-538 [PMID: 30870812]
  24. Front Endocrinol (Lausanne). 2022 Sep 06;13:981622 [PMID: 36147570]
  25. Transl Oncol. 2023 Jan;27:101571 [PMID: 36401966]
  26. Cancer Biomark. 2017;18(1):87-94 [PMID: 28085013]
  27. Biomed Rep. 2020 Jan;12(1):11-16 [PMID: 31839944]
  28. J Endocrinol Invest. 2021 May;44(5):883-890 [PMID: 33332019]
  29. Front Genet. 2022 Jun 30;13:865472 [PMID: 35846122]
  30. Front Genet. 2022 Sep 13;13:978840 [PMID: 36186442]
  31. Endokrynol Pol. 2021;72(6):676-677 [PMID: 34647614]
  32. Pharmacol Res. 2021 Dec;174:105941 [PMID: 34656765]
  33. Front Immunol. 2022 Aug 25;13:967914 [PMID: 36110849]
  34. Front Pharmacol. 2022 Oct 10;13:1003684 [PMID: 36299891]
  35. J Clin Med. 2022 Oct 27;11(21): [PMID: 36362565]
  36. Hum Gene Ther. 2019 May;30(5):618-631 [PMID: 30375256]
  37. J Biochem. 2021 Oct 11;170(2):195-202 [PMID: 34562091]
  38. Biomark Res. 2022 Jun 4;10(1):40 [PMID: 35659780]
  39. Int J Immunopathol Pharmacol. 2018 Jan-Dec;32:2058738418772652 [PMID: 29856242]
  40. J Surg Oncol. 2018 Sep;118(3):501-509 [PMID: 30132912]
  41. Genes (Basel). 2022 Jan 19;13(2): [PMID: 35205216]
  42. BMC Cancer. 2021 Mar 15;21(1):273 [PMID: 33722206]

Word Cloud

Created with Highcharts 10.0.0thyroiddisease=childrenvsamol/��LmoleculespatientsmiR-15a-5pmiR-126-3pmiR-142-5pnodular0miR-21-5pmiR-150-5pbloodlevelscomparedgroup3diseasesthyroiditisGraves'studycontrolmolecule147epigeneticgeneexpressionsmiRNAsautoimmuneHashimoto'spredisposecancerdevelopment20groupsadolescentsstatisticallysignificantexpression502204GDfocallesionsglandBACKGROUND:ManyfactorsincludingmicroRNAsinvolvedprocesschangingSmallnon-codingRNAcalledresponsibleregulatingtranslationsilencingdegradingtargetmRNAsacknowledgedmanymaynoveldiagnosticprognosticbiomarkersPatientslikelydevelopnodulestissueevaluatedconcentrationsmicroRNAdisordersadditionwishedidentifywhosechangeconcentrationpredisposesAIM:aimevaluateselectedelementsanalyzingpediatric2526healthy17MATERIALSANDMETHODS:consistsaged10-18yearsdeterminedimmunoenzymaticassayusingBioVendorreagentsRESULTS:decrease216103controls23HigherfoundGD-3801HT-3NSdisease-416Lowernoted092402changesobservedCONCLUSIONS:1overexpressionoccurs2DecreasedformationIdentifyinglowerrequirescarefulfollow-upevaluationpotentialmalignancyPotentialRoleSelectedPathogenesisAutoimmuneThyroidDiseasesChildrenAdolescentsGraves���Hashimoto���smiRNA

Similar Articles

Cited By