Cargando…

Extracellular Mechanical Stimuli Alters the Metastatic Progression of Prostate Cancer Cells within 3D Tissue Matrix

This study aimed to understand extracellular mechanical stimuli’s effect on prostate cancer cells’ metastatic progression within a three-dimensional (3D) bone-like microenvironment. In this study, a mechanical loading platform, EQUicycler, has been employed to create physiologically relevant static...

Descripción completa

Detalles Bibliográficos
Autores principales: Ditto, Maggie, Jacho, Diego, Eisenmann, Kathryn M., Yildirim-Ayan, Eda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669840/
https://www.ncbi.nlm.nih.gov/pubmed/38002395
http://dx.doi.org/10.3390/bioengineering10111271
_version_ 1785139786350067712
author Ditto, Maggie
Jacho, Diego
Eisenmann, Kathryn M.
Yildirim-Ayan, Eda
author_facet Ditto, Maggie
Jacho, Diego
Eisenmann, Kathryn M.
Yildirim-Ayan, Eda
author_sort Ditto, Maggie
collection PubMed
description This study aimed to understand extracellular mechanical stimuli’s effect on prostate cancer cells’ metastatic progression within a three-dimensional (3D) bone-like microenvironment. In this study, a mechanical loading platform, EQUicycler, has been employed to create physiologically relevant static and cyclic mechanical stimuli to a prostate cancer cell (PC-3)-embedded 3D tissue matrix. Three mechanical stimuli conditions were applied: control (no loading), cyclic (1% strain at 1 Hz), and static mechanical stimuli (1% strain). The changes in prostate cancer cells’ cytoskeletal reorganization, polarity (elongation index), proliferation, expression level of N-Cadherin (metastasis-associated gene), and migratory potential within the 3D collagen structures were assessed upon mechanical stimuli. The results have shown that static mechanical stimuli increased the metastasis progression factors, including cell elongation (p < 0.001), cellular F-actin accumulation (p < 0.001), actin polymerization (p < 0.001), N-Cadherin gene expression, and invasion capacity of PC-3 cells within a bone-like microenvironment compared to its cyclic and control loading counterparts. This study established a novel system for studying metastatic cancer cells within bone and enables the creation of biomimetic in vitro models for cancer research and mechanobiology.
format Online
Article
Text
id pubmed-10669840
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-106698402023-10-31 Extracellular Mechanical Stimuli Alters the Metastatic Progression of Prostate Cancer Cells within 3D Tissue Matrix Ditto, Maggie Jacho, Diego Eisenmann, Kathryn M. Yildirim-Ayan, Eda Bioengineering (Basel) Article This study aimed to understand extracellular mechanical stimuli’s effect on prostate cancer cells’ metastatic progression within a three-dimensional (3D) bone-like microenvironment. In this study, a mechanical loading platform, EQUicycler, has been employed to create physiologically relevant static and cyclic mechanical stimuli to a prostate cancer cell (PC-3)-embedded 3D tissue matrix. Three mechanical stimuli conditions were applied: control (no loading), cyclic (1% strain at 1 Hz), and static mechanical stimuli (1% strain). The changes in prostate cancer cells’ cytoskeletal reorganization, polarity (elongation index), proliferation, expression level of N-Cadherin (metastasis-associated gene), and migratory potential within the 3D collagen structures were assessed upon mechanical stimuli. The results have shown that static mechanical stimuli increased the metastasis progression factors, including cell elongation (p < 0.001), cellular F-actin accumulation (p < 0.001), actin polymerization (p < 0.001), N-Cadherin gene expression, and invasion capacity of PC-3 cells within a bone-like microenvironment compared to its cyclic and control loading counterparts. This study established a novel system for studying metastatic cancer cells within bone and enables the creation of biomimetic in vitro models for cancer research and mechanobiology. MDPI 2023-10-31 /pmc/articles/PMC10669840/ /pubmed/38002395 http://dx.doi.org/10.3390/bioengineering10111271 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
Ditto, Maggie
Jacho, Diego
Eisenmann, Kathryn M.
Yildirim-Ayan, Eda
Extracellular Mechanical Stimuli Alters the Metastatic Progression of Prostate Cancer Cells within 3D Tissue Matrix
title Extracellular Mechanical Stimuli Alters the Metastatic Progression of Prostate Cancer Cells within 3D Tissue Matrix
title_full Extracellular Mechanical Stimuli Alters the Metastatic Progression of Prostate Cancer Cells within 3D Tissue Matrix
title_fullStr Extracellular Mechanical Stimuli Alters the Metastatic Progression of Prostate Cancer Cells within 3D Tissue Matrix
title_full_unstemmed Extracellular Mechanical Stimuli Alters the Metastatic Progression of Prostate Cancer Cells within 3D Tissue Matrix
title_short Extracellular Mechanical Stimuli Alters the Metastatic Progression of Prostate Cancer Cells within 3D Tissue Matrix
title_sort extracellular mechanical stimuli alters the metastatic progression of prostate cancer cells within 3d tissue matrix
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669840/
https://www.ncbi.nlm.nih.gov/pubmed/38002395
http://dx.doi.org/10.3390/bioengineering10111271
work_keys_str_mv AT dittomaggie extracellularmechanicalstimulialtersthemetastaticprogressionofprostatecancercellswithin3dtissuematrix
AT jachodiego extracellularmechanicalstimulialtersthemetastaticprogressionofprostatecancercellswithin3dtissuematrix
AT eisenmannkathrynm extracellularmechanicalstimulialtersthemetastaticprogressionofprostatecancercellswithin3dtissuematrix
AT yildirimayaneda extracellularmechanicalstimulialtersthemetastaticprogressionofprostatecancercellswithin3dtissuematrix