Exosomes released upon mitochondrial ASncmtRNA knockdown reduce tumorigenic properties of malignant breast cancer cells

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dc.contributor.authorLobos-González, Lorena
dc.contributor.authorBustos, Rocío
dc.contributor.authorCampos, América
dc.contributor.authorSilva, Valeria
dc.contributor.authorSilva, Verónica
dc.contributor.authorJeldes, Emanuel
dc.contributor.authorSalomon, Carlos
dc.contributor.authorVaras-Godoy, Manuel
dc.contributor.authorCáceres-Verschae, Albano
dc.contributor.authorDuran, Eduardo
dc.contributor.authorVera, Tamara
dc.contributor.authorEzquer, Fernando
dc.date.accessioned2023-04-24T20:07:51Z
dc.date.available2023-04-24T20:07:51Z
dc.date.issued2020-12
dc.descriptionIndexación: Scopus.es
dc.description.abstractDuring 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 modeles
dc.description.urihttps://www-nature-com.recursosbiblioteca.unab.cl/articles/s41598-019-57018-1
dc.identifier.citationScientific Reports Volume 10, Issue 11 December 2020 Article number 343es
dc.identifier.doi10.1038/s41598-019-57018-1
dc.identifier.issn2045-2322
dc.identifier.urihttps://repositorio.unab.cl/xmlui/handle/ria/48879
dc.language.isoenes
dc.publisherNature Researches
dc.rights.licenseAtribution 4.0 International (CC BY 4.0)
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/deed.es
dc.subjectRNA (ASncmtRNA)es
dc.subjectExtracellular Vesicleses
dc.subjectMetastatices
dc.subjectBreast Canceres
dc.subjectTumorigenesises
dc.subjectCancer Cellses
dc.titleExosomes released upon mitochondrial ASncmtRNA knockdown reduce tumorigenic properties of malignant breast cancer cellses
dc.typeArtículoes
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