Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/54830
Campo DC Valoridioma
dc.contributor.authorOnstenk, Wendyen_US
dc.contributor.authorSieuwerts, Anieta M.en_US
dc.contributor.authorMostert, Biancaen_US
dc.contributor.authorLalmahomed, Zarinaen_US
dc.contributor.authorBolt-de Vries, Joan B.en_US
dc.contributor.authorvan Galen, Anneen_US
dc.contributor.authorSmid, Marcelen_US
dc.contributor.authorKraan, Jacoen_US
dc.contributor.authorVan, Maien_US
dc.contributor.authorde Weerd, Vanjaen_US
dc.contributor.authorRamírez-Moreno, Raquelen_US
dc.contributor.authorBiermann, Katharinaen_US
dc.contributor.authorVerhoef, Cornelisen_US
dc.contributor.authorGrünhagen, Dirk J.en_US
dc.contributor.authorIjzermans, Jan N.M.en_US
dc.contributor.authorGratama, Jan W.en_US
dc.contributor.authorMartens, John W.M.en_US
dc.contributor.authorFoekens, John A.en_US
dc.contributor.authorSleijfer, Stefanen_US
dc.date.accessioned2019-02-18T15:03:26Z-
dc.date.available2019-02-18T15:03:26Z-
dc.date.issued2016en_US
dc.identifier.issn1949-2553en_US
dc.identifier.urihttp://hdl.handle.net/10553/54830-
dc.description.abstractBackground: CTCs are a promising alternative for metastatic tissue biopsies for use in precision medicine approaches. We investigated to what extent the molecular characteristics of circulating tumor cells (CTCs) resemble the liver metastasis and/or the primary tumor from patients with metastatic colorectal cancer (mCRC). Results: The CTC profiles were concordant with the liver metastasis in 17/23 patients (74%) and with the primary tumor in 13 patients (57%). The CTCs better resembled the liver metastasis in 13 patients (57%), and the primary tumor in five patients (22%). The strength of the correlations was not associated with clinical parameters. Nine genes (CDH1, CDH17, CDX1, CEACAM5, FABP1, FCGBP, IGFBP3, IGFBP4, and MAPT) displayed significant differential expressions, all of which were downregulated, in CTCs compared to the tissues in the 23 patients. Patients and Methods: Patients were retrospectively selected from a prospective study. Using the CellSearch System, CTCs were enumerated and isolated just prior to liver metastasectomy. A panel of 25 CTC-specific genes was measured by RT-qPCR in matching CTCs, primary tumors, and liver metastases. Spearman correlation coefficients were calculated and considered as continuous variables with r=1 representing absolute concordance and r=-1 representing absolute discordance. A cut-off of r>0.1 was applied in order to consider profiles to be concordant. Conclusions: In the majority of the patients, CTCs reflected the molecular characteristics of metastatic cells better than the primary tumors. Genes involved in cell adhesion and epithelial-to-mesenchymal transition were downregulated in the CTCs. Our results support the use of CTC characterization as a liquid biopsy for precision medicine.en_US
dc.languageengen_US
dc.relation.ispartofOncotargeten_US
dc.sourceOncotarget [ISSN 1949-2553], v. 7, p. 59058-59069en_US
dc.subject320713 Oncologíaen_US
dc.titleMolecular characteristics of circulating tumor cells resemble the liver metastasis more closely than the primary tumor in metastatic colorectal canceren_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.18632/oncotarget.10175en_US
dc.identifier.scopus84991289802-
dc.contributor.authorscopusid36673653300-
dc.contributor.authorscopusid6602157921-
dc.contributor.authorscopusid24169623900-
dc.contributor.authorscopusid25936311400-
dc.contributor.authorscopusid6603538971-
dc.contributor.authorscopusid36648001000-
dc.contributor.authorscopusid7006398514-
dc.contributor.authorscopusid7003751962-
dc.contributor.authorscopusid56576114300-
dc.contributor.authorscopusid14017743600-
dc.contributor.authorscopusid25959711200-
dc.contributor.authorscopusid23466545100-
dc.contributor.authorscopusid7003616369-
dc.contributor.authorscopusid57190335531-
dc.contributor.authorscopusid7005305323-
dc.contributor.authorscopusid24733628000-
dc.contributor.authorscopusid7201836882-
dc.contributor.authorscopusid7006484454-
dc.contributor.authorscopusid6601983607-
dc.description.lastpage59069en_US
dc.description.firstpage59058en_US
dc.relation.volume7en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.utils.revisionen_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr1,927
dc.description.jcr5,168
dc.description.sjrqQ1
dc.description.jcrqQ1
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Farmacología Molecular y Traslacional-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameRamirez Moreno,Raquel-
Colección:Artículos
Vista resumida

Citas SCOPUSTM   

37
actualizado el 17-nov-2024

Citas de WEB OF SCIENCETM
Citations

30
actualizado el 17-nov-2024

Visitas

61
actualizado el 24-feb-2024

Google ScholarTM

Verifica

Altmetric


Comparte



Exporta metadatos



Los elementos en ULPGC accedaCRIS están protegidos por derechos de autor con todos los derechos reservados, a menos que se indique lo contrario.