Heterotypic signaling between dermal fibroblasts and melanoma cells induces phenotypic plasticity and proteome rearrangement in malignant cells

dc.citation.issue12pt_BR
dc.citation.volume1868pt_BR
dc.contributor.authorPessotti, Dayelle [UNIFESP]
dc.contributor.authorAndrade-Silva, Débora - Instituto Butantan
dc.contributor.authorSerrano, Solange - Instituto Butantan
dc.contributor.authorZelanis, André [UNIFESP]
dc.contributor.authorLatteshttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4778207Z4pt_BR
dc.date.accessioned2021-03-16T11:36:18Z
dc.date.available2021-03-16T11:36:18Z
dc.date.issued2020-08-29
dc.description.abstractThe signaling events triggered by soluble mediators released from both transformed and stromal cells shape the phenotype of tumoral cells and have significant implications in cancer development and progression. In this study we performed an in vitro heterotypic signaling assays by evaluating the proteome diversity of human dermal fibroblasts after stimulation with the conditioned media obtained from malignant melanoma cells. In addition, we also evaluated the changes in the proteome of melanoma cells after stimulation with their own conditioned media as well as with the conditioned medium from melanoma-stimulated fibroblasts. Our results revealed a clear rearrangement in the proteome of stromal and malignant cells upon crosstalk of soluble mediators. The main proteome signature of fibroblasts stimulated with melanoma conditioned medium was related to protein synthesis, which indicates that this process might be an early response of stromal cells. In addition, the conditioned medium derived from ‘primed’ stromal cells (melanoma-stimulated fibroblasts) was more effective in altering the functional phenotype (cell migration) of malignant cells than the conditioned medium from nonstimulated fibroblasts. Collectively, self- and cross-stimulation may play a key role in shaping the tumor microenvironment and enable tumoral cells to succeed in the process of melanoma progression and metastasis. Although the proteome landscape of cells participating in such a heterotypic signaling represents a snapshot of a highly dynamic state, understanding the diversity of proteins and enriched biological pathways resulting from stimulated cell states may allow for targeting specific cell regulatory motifs involved in melanoma progression and metastasis.pt_BR
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dc.description.provenanceMade available in DSpace on 2021-03-16T11:36:18Z (GMT). No. of bitstreams: 1 Pessotti et al 2020.pdf: 4092952 bytes, checksum: b0b7fdd226d011d7d6cecf74313e59b4 (MD5) Previous issue date: 2020-08-29en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)pt_BR
dc.description.sponsorshipID2014/06579-3, 2013/07467-1, 2016/16935-7, 2019/07282-8pt_BR
dc.format.extent140525pt_BR
dc.identifierhttps://www.sciencedirect.com/science/article/pii/S1570963920301722?via%3Dihubpt_BR
dc.identifier.doihttps://doi.org/10.1016/j.bbapap.2020.140525pt_BR
dc.identifier.issn1570-9639pt_BR
dc.identifier.urihttps://repositorio.unifesp.br/handle/11600/60497
dc.languageengpt_BR
dc.publisherUlrich Brandtpt_BR
dc.relation.ispartofBiochimica et Biophysica Acta (BBA) - Proteins and Proteomicspt_BR
dc.rightsAcesso abertopt_BR
dc.subjectheterotypic signalingpt_BR
dc.subjectmelanomapt_BR
dc.subjectfibroblastpt_BR
dc.subjectCancer-associated fibroblastspt_BR
dc.subjectphenotypic plasticitypt_BR
dc.titleHeterotypic signaling between dermal fibroblasts and melanoma cells induces phenotypic plasticity and proteome rearrangement in malignant cellspt_BR
dc.typeArtigopt_BR
unifesp.assessoresproreitoriasNão se aplicapt_BR
unifesp.campusInstituto de Ciência e Tecnologia (ICT)pt_BR
unifesp.departamentoCiência e Tecnologiapt_BR
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