Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/113116
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dc.contributor.authorSampaio-Ribeiro, Gabriela-
dc.contributor.authorRuivo, Ana-
dc.contributor.authorSilva, Ana-
dc.contributor.authorSantos, Ana Lúcia-
dc.contributor.authorOliveira, Rui Caetano-
dc.contributor.authorGama, João-
dc.contributor.authorCipriano, Maria Augusta-
dc.contributor.authorTralhão, José Guilherme-
dc.contributor.authorPaiva, Artur-
dc.date.accessioned2024-02-06T09:45:42Z-
dc.date.available2024-02-06T09:45:42Z-
dc.date.issued2023-06-16-
dc.identifier.issn2072-6694-
dc.identifier.urihttps://hdl.handle.net/10316/113116-
dc.description.abstractColorectal cancer (CRC) is the third most prevalent type of cancer, and liver metastasis is the most common site of metastatic development. In the tumor microenvironment (TME), various innate immune cells are known to influence cancer progression and metastasis occurrence. CD274 (PD-L1) and CD206 (MRC1) are proteins that have been associated with poor prognosis and disease progression. We conducted a study on tumoral and non-tumoral biopsies from 47 patients with CRC liver metastasis, using flow cytometry to phenotypically characterize innate immune cells. Our findings showed an increase in the expression of CD274 on classical, intermediate, and non-classical monocytes when comparing tumor with non-tumor samples. Furthermore, tumor samples with a desmoplastic growth pattern exhibited a significantly decreased percentage of CD274- and CD206-positive cells in all monocyte populations compared to non-desmoplastic samples. We found a correlation between a lower expression of CD206 or CD274 on classical, intermediate, and non-classical monocytes and increased disease-free survival, which points to a better prognosis for these patients. In conclusion, our study has identified potential new targets and biomarkers that could be incorporated into a personalized medicine approach to enhance the outcome for colorectal cancer patients.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationUI/BD/154407/2022pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectcolorectal cancerpt
dc.subjectlivermetastasispt
dc.subjectinnate immune systempt
dc.subjectmonocytespt
dc.subjectpersonalized medicinept
dc.titleInnate Immune Cells in the Tumor Microenvironment of Liver Metastasis from Colorectal Cancer: Contribution to a Comprehensive Therapypt
dc.typearticlept
degois.publication.firstPage3222pt
degois.publication.issue12pt
degois.publication.titleCancerspt
dc.peerreviewedyespt
dc.identifier.doi10.3390/cancers15123222-
degois.publication.volume15pt
dc.date.embargo2023-06-16*
dc.identifier.pmid37370832-
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.orcid0000-0002-7202-8059-
crisitem.author.orcid0000-0002-6562-5859-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
I&D CIBB - Artigos em Revistas Internacionais
I&D ICBR - Artigos em Revistas Internacionais
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