Bone microenvironment provides growth and survival signals essential for osteosarcoma (OS) initiation and progression. OS cells regulate communications inside tumor microenvironment through different ways and, among all, tumor-derived exosomes support cancer progression and metastasis. To define the contribution of OS-derived exosomes inside the microenvironment, we investigated the effects induced in bone remodeling mechanism and tumor angiogenesis. We demonstrated that exosomes promoted osteoclasts differentiation and bone resorption activity. Furthermore, exosomes potentiated tube formation of endothelial cells and increased angiogenic markers expression. We therefore investigated the micro RNA (miRNA) cargo from exosomes and their parental cells by performing small RNA sequencing through NGS Illumina platform. Hierarchical clustering highlighted a unique molecular profile of exosomal miRNA; bioinformatic analysis by DIANA-mirPath revealed that miRNAs identified take part in various biological processes and carcinogenesis. Among these miRNAs, some were already known for their involvement in the tumor microenvironment establishment, as miR-148a and miR-21-5p. Enforced expression of miR-148a and miR-21-5p in Raw264.7 and hTert immortalized umbilical vein endothelial cells recapitulated the effects induced by exosomes. Overall, our study highlighted the importance of OS exosomes in tumor microenvironment also by a specific packaging of miRNAs.

Osteosarcoma cell-derived exosomes affect tumor microenvironment by specific packaging of microRNAs

Manno M;Raccosta S;
2020

Abstract

Bone microenvironment provides growth and survival signals essential for osteosarcoma (OS) initiation and progression. OS cells regulate communications inside tumor microenvironment through different ways and, among all, tumor-derived exosomes support cancer progression and metastasis. To define the contribution of OS-derived exosomes inside the microenvironment, we investigated the effects induced in bone remodeling mechanism and tumor angiogenesis. We demonstrated that exosomes promoted osteoclasts differentiation and bone resorption activity. Furthermore, exosomes potentiated tube formation of endothelial cells and increased angiogenic markers expression. We therefore investigated the micro RNA (miRNA) cargo from exosomes and their parental cells by performing small RNA sequencing through NGS Illumina platform. Hierarchical clustering highlighted a unique molecular profile of exosomal miRNA; bioinformatic analysis by DIANA-mirPath revealed that miRNAs identified take part in various biological processes and carcinogenesis. Among these miRNAs, some were already known for their involvement in the tumor microenvironment establishment, as miR-148a and miR-21-5p. Enforced expression of miR-148a and miR-21-5p in Raw264.7 and hTert immortalized umbilical vein endothelial cells recapitulated the effects induced by exosomes. Overall, our study highlighted the importance of OS exosomes in tumor microenvironment also by a specific packaging of miRNAs.
2020
Istituto di Biofisica - IBF
alkaline phosphatase
calnexin
cathepsin K
CD81 antigen
interleukin 6
interleukin 8
messenger RNA
microRNA
microRNA 125a
microRNA 126
microRNA 128
microRNA 148a
microRNA 151a
microRNA 16
microRNA 182
microRNA 186
microRNA 1908
microRNA 193b
microRNA 21
microRNA 214
microRNA 23a
microRNA 301a
microRNA 331
microRNA 941
osteopontin
transcription factor RUNX2
unclassified drug
vasculotropin A
microRNA
tumor marker
animal cell
Article
biological phenomena and functions concerning the entire organism
bone remodeling
cancer growth
carcinogenesis
cell differentiation
computer model
confocal microscopy
controlled study
down regulation
endothelium cell
enzyme linked immunosorbent assay
exosome
gene expression
hierarchical clustering
human
human cell
in vitro study
MG-63 cell line
nonhuman
osteoclast
osteoclastogenesis
osteolysis
osteosarcoma cell
overall survival
photon correlation spectroscopy
polyacrylamide gel electrophoresis
priority journal
protein expression
real time polymerase chain reaction
RNA fingerprinting
RNA sequencing
SaOS-2 cell line
tumor microenvironment
U2OS cell line
umbilical vein endothelial cell
upregulation
Western blotting
bone tumor
cell culture
cell motion
cell proliferation
exosome
gene expression profiling
gene expression regulation
genetics
metabolism
neovascularization (pathology)
osteosarcoma
pathology
tumor microenvironment
vascular endothelium
Biomarkers
Tumor
Bone Neoplasms
Cell Movement
Cell Proliferation
Cells
Cultured
Endothelium
Vascular
Exosomes
Gene Expression Profiling
Gene Expression Regulation
Neoplastic
Humans
MicroRNAs
Neovascularization
Pathologic
Osteosarcoma
Tumor Microenvironment
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/415455
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