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dc.contributor.authorRoca Lema, Daniel
dc.contributor.authorMartínez Iglesias, Olaia Antía
dc.contributor.authorFernandez de Ana Portela, Catalina
dc.contributor.authorRodriguez-Blanco, Arturo
dc.contributor.authorValladares Ayerbes, Manuel 
dc.contributor.authorDíaz Díaz, Andrea
dc.contributor.authorCasas Pais, Alba
dc.contributor.authorPrego, Cecilia
dc.contributor.authorFigueroa Conde-Valvís, Angélica
dc.date.accessioned2022-01-27T10:39:51Z
dc.date.available2022-01-27T10:39:51Z
dc.date.issued2019
dc.identifier.issn1449-1907
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367522/pdf/ijmsv16p0231.pdfes
dc.identifier.urihttp://hdl.handle.net/20.500.11940/15954
dc.description.abstractColorectal cancer (CRC) is one of leading causes of mortality in western countries and novel treatment strategies are required. The medicinal application of mushrooms has been used in traditional medicine in many oriental countries. Polysaccharide-rich extracts obtained from certain medicinal mushroom species have shown antitumor effects in different experimental models. In the present study, we have developed polysaccharide-rich extracts from Trametes versicolor (TV) and Grifola frondosa (GF) fruit bodies. We aim to evaluate the anticancer effects of these polysaccharide-rich extracts in LoVo and HT-29 human colon cancer cells. The in vitro effects were determined by cytotoxicity assay, proliferation assay, wound healing assay and invasion assay. Moreover, the effect on anchorage independent-cell growth was also determined. Our results showed that TV and GF extracts did inhibit human colon cell proliferation and induce cytotoxicity. Furthermore, both fungal extracts significantly inhibited oncogenic potential, cell migration and invasion in colon cancer cells. In addition, extracts induce a more epithelial phenotype, observed by phase contrast images, together with an increase expression of the E-cadherin epithelial marker, detected by western-blotting analyses. Moreover, by using gelatin zymography assays, it was detected a decrease of MMP-2 enzyme activity, a crucial metalloproteinase important for the degradation of the extracellular matrix. Finally, the combination of the extracts with one the most clinical used agents for colorectal cancer, 5-fluorouracil, increases cell cytotoxicity. Taken together our results underscore a potential antitumor effect of polysaccharide-rich extracts obtained from TV and GF in human colon cancer cells lines. These finding may contribute to the reported health effects of fungal extracts.en
dc.language.isoenges
dc.rightsAtribución-NoComercial 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subject.meshAntimetabolites*
dc.subject.meshFluorouracil*
dc.subject.meshAdenocarcinoma*
dc.subject.meshCell Proliferation*
dc.subject.meshHT29 Cells*
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols*
dc.subject.meshTrametes*
dc.subject.meshCadherins*
dc.subject.meshBiological Products*
dc.subject.meshGrifola*
dc.subject.meshHumans*
dc.subject.meshCell Movement*
dc.subject.meshMatrix Metalloproteinase 2*
dc.subject.meshColorectal Neoplasms*
dc.titleIn Vitro Anti-proliferative and Anti-invasive Effect of Polysaccharide-rich Extracts from Trametes Versicolor and Grifola Frondosa in Colon Cancer Cellsen
dc.typeArtigoes
dc.identifier.doiijmsv16p0231
dc.identifier.pmid30745803
dc.identifier.sophos32625
dc.issue.number2es
dc.journal.titleInternational Journal of Medical Scienceses
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::Instituto de Investigación Biomédica da Coruña (INIBIC)es
dc.rights.accessRightsopenAccesses
dc.subject.decsfluorouracilo*
dc.subject.decsantimetabolitos*
dc.subject.decsGrifola*
dc.subject.decscélulas HT29*
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada*
dc.subject.decsproductos biológicos*
dc.subject.decsTrametes*
dc.subject.decsmovimiento celular*
dc.subject.decsproliferación celular*
dc.subject.decshumanos*
dc.subject.decscadherinas*
dc.subject.decsadenocarcinoma*
dc.subject.decsneoplasias colorrectales*
dc.subject.decsmetaloproteinasa 2 de la matriz*
dc.subject.keywordINIBICes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number16es


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