Cargando…

Two oncomiRs, miR-182-5p and miR-103a-3p, Involved in Intravenous Leiomyomatosis

Leiomyomas, also referred to as fibroids, belong to the most common type of benign tumors developing in the myometrium of the uterus. Intravenous leiomyomatosis (IVL) tends to be regarded as a rare type of uterine leiomyoma. IVL tumors are characterized by muscle cell masses developing within the ut...

Descripción completa

Detalles Bibliográficos
Autores principales: Barnaś, Edyta, Skręt-Magierło, Joanna Ewa, Paszek, Sylwia, Kaznowska, Ewa, Potocka, Natalia, Skręt, Andrzej, Sakowicz, Agata, Zawlik, Izabela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10048324/
https://www.ncbi.nlm.nih.gov/pubmed/36980984
http://dx.doi.org/10.3390/genes14030712
_version_ 1785014155098456064
author Barnaś, Edyta
Skręt-Magierło, Joanna Ewa
Paszek, Sylwia
Kaznowska, Ewa
Potocka, Natalia
Skręt, Andrzej
Sakowicz, Agata
Zawlik, Izabela
author_facet Barnaś, Edyta
Skręt-Magierło, Joanna Ewa
Paszek, Sylwia
Kaznowska, Ewa
Potocka, Natalia
Skręt, Andrzej
Sakowicz, Agata
Zawlik, Izabela
author_sort Barnaś, Edyta
collection PubMed
description Leiomyomas, also referred to as fibroids, belong to the most common type of benign tumors developing in the myometrium of the uterus. Intravenous leiomyomatosis (IVL) tends to be regarded as a rare type of uterine leiomyoma. IVL tumors are characterized by muscle cell masses developing within the uterine and extrauterine venous system. The underlying mechanism responsible for the proliferation of these lesions is still unknown. The aim of the study was to investigate the expression of the two epigenetic factors, oncomiRs miR-182-5p and miR-103a-3p, in intravenous leiomyomatosis. This study was divided into two stages: initially, miR-182-5p and miR-103a-3p expression was assessed in samples coming from intravenous leiomyomatosis localized in myometrium (group I, n = 6), intravenous leiomyomatosis beyond the uterus (group II; n = 5), and the control group, i.e., intramural leiomyomas (group III; n = 9). The expression level of miR-182-5p was significantly higher in samples coming from intravenous leiomyomatosis (group I and group II) as compared to the control group (p = 0.029 and p = 0.024, respectively). In the second part of the study, the expression levels of the studied oncomiRs were compared between seven samples delivered from one woman during a four-year observation. The long-term follow-up of one patient demonstrated significantly elevated levels of both studied oncomiRs in intravenous leiomyomatosis in comparison to intramural leiomyoma samples.
format Online
Article
Text
id pubmed-10048324
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-100483242023-03-29 Two oncomiRs, miR-182-5p and miR-103a-3p, Involved in Intravenous Leiomyomatosis Barnaś, Edyta Skręt-Magierło, Joanna Ewa Paszek, Sylwia Kaznowska, Ewa Potocka, Natalia Skręt, Andrzej Sakowicz, Agata Zawlik, Izabela Genes (Basel) Article Leiomyomas, also referred to as fibroids, belong to the most common type of benign tumors developing in the myometrium of the uterus. Intravenous leiomyomatosis (IVL) tends to be regarded as a rare type of uterine leiomyoma. IVL tumors are characterized by muscle cell masses developing within the uterine and extrauterine venous system. The underlying mechanism responsible for the proliferation of these lesions is still unknown. The aim of the study was to investigate the expression of the two epigenetic factors, oncomiRs miR-182-5p and miR-103a-3p, in intravenous leiomyomatosis. This study was divided into two stages: initially, miR-182-5p and miR-103a-3p expression was assessed in samples coming from intravenous leiomyomatosis localized in myometrium (group I, n = 6), intravenous leiomyomatosis beyond the uterus (group II; n = 5), and the control group, i.e., intramural leiomyomas (group III; n = 9). The expression level of miR-182-5p was significantly higher in samples coming from intravenous leiomyomatosis (group I and group II) as compared to the control group (p = 0.029 and p = 0.024, respectively). In the second part of the study, the expression levels of the studied oncomiRs were compared between seven samples delivered from one woman during a four-year observation. The long-term follow-up of one patient demonstrated significantly elevated levels of both studied oncomiRs in intravenous leiomyomatosis in comparison to intramural leiomyoma samples. MDPI 2023-03-14 /pmc/articles/PMC10048324/ /pubmed/36980984 http://dx.doi.org/10.3390/genes14030712 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Barnaś, Edyta
Skręt-Magierło, Joanna Ewa
Paszek, Sylwia
Kaznowska, Ewa
Potocka, Natalia
Skręt, Andrzej
Sakowicz, Agata
Zawlik, Izabela
Two oncomiRs, miR-182-5p and miR-103a-3p, Involved in Intravenous Leiomyomatosis
title Two oncomiRs, miR-182-5p and miR-103a-3p, Involved in Intravenous Leiomyomatosis
title_full Two oncomiRs, miR-182-5p and miR-103a-3p, Involved in Intravenous Leiomyomatosis
title_fullStr Two oncomiRs, miR-182-5p and miR-103a-3p, Involved in Intravenous Leiomyomatosis
title_full_unstemmed Two oncomiRs, miR-182-5p and miR-103a-3p, Involved in Intravenous Leiomyomatosis
title_short Two oncomiRs, miR-182-5p and miR-103a-3p, Involved in Intravenous Leiomyomatosis
title_sort two oncomirs, mir-182-5p and mir-103a-3p, involved in intravenous leiomyomatosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10048324/
https://www.ncbi.nlm.nih.gov/pubmed/36980984
http://dx.doi.org/10.3390/genes14030712
work_keys_str_mv AT barnasedyta twooncomirsmir1825pandmir103a3pinvolvedinintravenousleiomyomatosis
AT skretmagierłojoannaewa twooncomirsmir1825pandmir103a3pinvolvedinintravenousleiomyomatosis
AT paszeksylwia twooncomirsmir1825pandmir103a3pinvolvedinintravenousleiomyomatosis
AT kaznowskaewa twooncomirsmir1825pandmir103a3pinvolvedinintravenousleiomyomatosis
AT potockanatalia twooncomirsmir1825pandmir103a3pinvolvedinintravenousleiomyomatosis
AT skretandrzej twooncomirsmir1825pandmir103a3pinvolvedinintravenousleiomyomatosis
AT sakowiczagata twooncomirsmir1825pandmir103a3pinvolvedinintravenousleiomyomatosis
AT zawlikizabela twooncomirsmir1825pandmir103a3pinvolvedinintravenousleiomyomatosis