Exosomes released upon mitochondrial ASncmtRNA knockdown reduce tumorigenic properties of malignant breast cancer cells
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Archivos
Fecha
2020-12
Profesor/a Guía
Facultad/escuela
Idioma
en
Título de la revista
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Título del volumen
Editor
Nature Research
Nombre de Curso
Licencia CC
Atribution 4.0 International (CC BY 4.0)
Licencia CC
https://creativecommons.org/licenses/by/4.0/deed.es
Resumen
During intercellular communication, cells release extracellular vesicles such as exosomes, which contain
proteins, ncRNAs and mRNAs that can infuence proliferation and/or trigger apoptosis in recipient
cells, and have been proposed to play an essential role in promoting invasion of tumor cells and in
the preparation of metastatic niches. Our group proposed the antisense non-coding mitochondrial
RNA (ASncmtRNA) as a new target for cancer therapy. ASncmtRNA knockdown using an antisense
oligonucleotide (ASO-1537S) causes massive death of tumor cells but not normal cells and strongly
reduces metastasis in mice. In this work, we report that exosomes derived from ASO-1537S-treated
MDA-MB-231 breast cancer cells (Exo-1537S) inhibits tumorigenesis of recipient cells, in contrast to
exosomes derived from control-ASO-treated cells (Exo-C) which, in contrast, enhance these properties.
Furthermore, an in vivo murine peritoneal carcinomatosis model showed that Exo-1537S injection
reduced tumorigenicity compared to controls. Proteomic analysis revealed the presence of Lactadherin
and VE-Cadherin in exosomes derived from untreated cells (Exo-WT) and Exo-C but not in Exo-1537S,
and the latter displayed enrichment of proteasomal subunits. These results suggest a role for these
proteins in modulation of tumorigenic properties of exosome-recipient cells. Our results shed light
on the mechanisms through which ASncmtRNA knockdown afects the preparation of breast cancer
metastatic niches in a peritoneal carcinomatosis model
Notas
Indexación: Scopus.
Palabras clave
RNA (ASncmtRNA), Extracellular Vesicles, Metastatic, Breast Cancer, Tumorigenesis, Cancer Cells
Citación
Scientific Reports Volume 10, Issue 11 December 2020 Article number 343
DOI
10.1038/s41598-019-57018-1