Cargando…

Molecular Signature of Prospero Homeobox 1 (PROX1) in Follicular Thyroid Carcinoma Cells

The prospero homeobox 1 (PROX1) transcription factor is a product of one of the lymphangiogenesis master genes. It has also been suggested to play a role in carcinogenesis, although its precise role in tumour development and metastasis remains unclear. The aim of this study was to gain more knowledg...

Descripción completa

Detalles Bibliográficos
Autores principales: Rudzińska, Magdalena, Grzanka, Małgorzata, Stachurska, Anna, Mikula, Michał, Paczkowska, Katarzyna, Stępień, Tomasz, Paziewska, Agnieszka, Ostrowski, Jerzy, Czarnocka, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539481/
https://www.ncbi.nlm.nih.gov/pubmed/31060342
http://dx.doi.org/10.3390/ijms20092212
_version_ 1783422398971772928
author Rudzińska, Magdalena
Grzanka, Małgorzata
Stachurska, Anna
Mikula, Michał
Paczkowska, Katarzyna
Stępień, Tomasz
Paziewska, Agnieszka
Ostrowski, Jerzy
Czarnocka, Barbara
author_facet Rudzińska, Magdalena
Grzanka, Małgorzata
Stachurska, Anna
Mikula, Michał
Paczkowska, Katarzyna
Stępień, Tomasz
Paziewska, Agnieszka
Ostrowski, Jerzy
Czarnocka, Barbara
author_sort Rudzińska, Magdalena
collection PubMed
description The prospero homeobox 1 (PROX1) transcription factor is a product of one of the lymphangiogenesis master genes. It has also been suggested to play a role in carcinogenesis, although its precise role in tumour development and metastasis remains unclear. The aim of this study was to gain more knowledge on the PROX1 function in thyroid tumorigenesis. Follicular thyroid cancer-derived cells—CGTH-W-1—were transfected with PROX1-siRNA (small interfering RNA) and their proliferation, cell cycle, apoptosis and motility were then analysed. The transcriptional signature of PROX1 depletion was determined using RNA-Sequencing (RNA-Seq) and the expression of relevant genes was further validated using reverse transcriptase quantitative PCR (RT-qPCR), Western blot and immunocytochemistry. PROX1 depletion resulted in a decreased cell motility, with both migratory and invasive potential being significantly reduced. The cell morphology was also affected, while the other studied cancer-related cell characteristics were not significantly altered. RNA-seq analysis revealed significant changes in the expression of transcripts encoding genes involved in both motility and cytoskeleton organization. Our transcriptional analysis of PROX1-depleted follicular thyroid carcinoma cells followed by functional and phenotypical analyses provide, for the first time, evidence that PROX1 plays an important role in the metastasis of thyroid cancer cells by regulating genes involved in focal adhesion and cytoskeleton organization in tumour cells.
format Online
Article
Text
id pubmed-6539481
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-65394812019-06-04 Molecular Signature of Prospero Homeobox 1 (PROX1) in Follicular Thyroid Carcinoma Cells Rudzińska, Magdalena Grzanka, Małgorzata Stachurska, Anna Mikula, Michał Paczkowska, Katarzyna Stępień, Tomasz Paziewska, Agnieszka Ostrowski, Jerzy Czarnocka, Barbara Int J Mol Sci Article The prospero homeobox 1 (PROX1) transcription factor is a product of one of the lymphangiogenesis master genes. It has also been suggested to play a role in carcinogenesis, although its precise role in tumour development and metastasis remains unclear. The aim of this study was to gain more knowledge on the PROX1 function in thyroid tumorigenesis. Follicular thyroid cancer-derived cells—CGTH-W-1—were transfected with PROX1-siRNA (small interfering RNA) and their proliferation, cell cycle, apoptosis and motility were then analysed. The transcriptional signature of PROX1 depletion was determined using RNA-Sequencing (RNA-Seq) and the expression of relevant genes was further validated using reverse transcriptase quantitative PCR (RT-qPCR), Western blot and immunocytochemistry. PROX1 depletion resulted in a decreased cell motility, with both migratory and invasive potential being significantly reduced. The cell morphology was also affected, while the other studied cancer-related cell characteristics were not significantly altered. RNA-seq analysis revealed significant changes in the expression of transcripts encoding genes involved in both motility and cytoskeleton organization. Our transcriptional analysis of PROX1-depleted follicular thyroid carcinoma cells followed by functional and phenotypical analyses provide, for the first time, evidence that PROX1 plays an important role in the metastasis of thyroid cancer cells by regulating genes involved in focal adhesion and cytoskeleton organization in tumour cells. MDPI 2019-05-05 /pmc/articles/PMC6539481/ /pubmed/31060342 http://dx.doi.org/10.3390/ijms20092212 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rudzińska, Magdalena
Grzanka, Małgorzata
Stachurska, Anna
Mikula, Michał
Paczkowska, Katarzyna
Stępień, Tomasz
Paziewska, Agnieszka
Ostrowski, Jerzy
Czarnocka, Barbara
Molecular Signature of Prospero Homeobox 1 (PROX1) in Follicular Thyroid Carcinoma Cells
title Molecular Signature of Prospero Homeobox 1 (PROX1) in Follicular Thyroid Carcinoma Cells
title_full Molecular Signature of Prospero Homeobox 1 (PROX1) in Follicular Thyroid Carcinoma Cells
title_fullStr Molecular Signature of Prospero Homeobox 1 (PROX1) in Follicular Thyroid Carcinoma Cells
title_full_unstemmed Molecular Signature of Prospero Homeobox 1 (PROX1) in Follicular Thyroid Carcinoma Cells
title_short Molecular Signature of Prospero Homeobox 1 (PROX1) in Follicular Thyroid Carcinoma Cells
title_sort molecular signature of prospero homeobox 1 (prox1) in follicular thyroid carcinoma cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6539481/
https://www.ncbi.nlm.nih.gov/pubmed/31060342
http://dx.doi.org/10.3390/ijms20092212
work_keys_str_mv AT rudzinskamagdalena molecularsignatureofprosperohomeobox1prox1infollicularthyroidcarcinomacells
AT grzankamałgorzata molecularsignatureofprosperohomeobox1prox1infollicularthyroidcarcinomacells
AT stachurskaanna molecularsignatureofprosperohomeobox1prox1infollicularthyroidcarcinomacells
AT mikulamichał molecularsignatureofprosperohomeobox1prox1infollicularthyroidcarcinomacells
AT paczkowskakatarzyna molecularsignatureofprosperohomeobox1prox1infollicularthyroidcarcinomacells
AT stepientomasz molecularsignatureofprosperohomeobox1prox1infollicularthyroidcarcinomacells
AT paziewskaagnieszka molecularsignatureofprosperohomeobox1prox1infollicularthyroidcarcinomacells
AT ostrowskijerzy molecularsignatureofprosperohomeobox1prox1infollicularthyroidcarcinomacells
AT czarnockabarbara molecularsignatureofprosperohomeobox1prox1infollicularthyroidcarcinomacells