dc.creatorVera, Sergio
dc.creatorSinning, Mariana
dc.creatorVergara, Marcela
dc.creatorLemus, David
dc.creatorRosas, Carlos
dc.date.accessioned2020-11-03T07:49:23Z
dc.date.accessioned2023-05-30T20:43:33Z
dc.date.available2020-11-03T07:49:23Z
dc.date.available2023-05-30T20:43:33Z
dc.date.created2020-11-03T07:49:23Z
dc.date.issued2019
dc.identifier0167-594X
dc.identifierhttp://dspace-uss.eastus.cloudapp.azure.com:8080/xmlui/handle/uss/335
dc.identifierhttp://dx.doi.org/10.1007/s11060-019-03314-9
dc.identifier1573-7373
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/6445496
dc.description.abstractIntroduction Gliomas are tumors of the central nervous system. Despite new classifications, they are still divided in low and high-grade gliomas, being the latter of greater malignancy. The degree of malignancy is directly related with the angiogenic activity in tumoral tissues. We measured VEGF concentrations and angiogenic capacity in cerebrospinal fluid (CSF) from patients with high and low-grade gliomas. The purpose of this study was to find a biomarker that contributes in the differential diagnosis and prognosis of gliomas. Methods CSF was obtained from 19 individuals: 8 with low-grade gliomas, 6 with high-grade gliomas and 5 controls. VEGF concentration in CSF was measured by ELISA and the angiogenic capacity was measured by chick chorioallantoic membrane (CAM) test. Results The VEGF concentration was higher in patients with high-grade gliomas, compared to patients with low-grade gliomas and controls (2860 pg/mL +/- 975 vs. 182.6 +/- 37.1 and 47.4 +/- 0.4, respectively). On the other hand, CSF from patients with high-grade gliomas generated a higher microvascular density (MVD) than patients with low-grade gliomas and controls (13.23 +/- 0.6 vessels/9000 mu m(2) vs. 9.3 +/- 0.3 and 7.92 +/- 0.2, respectively). Interestingly, there was not statistical differences in both VEGF levels and angiogenic capacity in patients with low-grade gliomas and controls. Conclusion Together VEGF levels and angiogenic capacity in CSF can be used as a biological marker of gliomas malignancy.
dc.languageen
dc.publisherFacultad de Medicina y Ciencia
dc.relationvol. 145, no. 2, p. 233-239
dc.relationIndexado en WOS
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile
dc.sourceJournal of Neuro-Oncology
dc.subjectANGIOGENESIS
dc.subjectGLIOMA
dc.subjectVEGF
dc.subjectBIOMARKER
dc.subjectCSF
dc.subjectENDOTHELIAL GROWTH-FACTOR
dc.subjectCENTRAL-NERVOUS-SYSTEM
dc.subjectMOLECULAR PATHOLOGY
dc.subjectCANCER
dc.subjectBRAIN
dc.subjectPROCARBAZINE
dc.subjectVINCRISTINE
dc.subjectTUMORS
dc.subjectEPIDEMIOLOGY
dc.subjectEXPRESSION
dc.titleCerebrospinal fluid VEGF levels and angiogenic capacity as potential prognostic markers in patients with gliomas: a pilot study
dc.typeArticle


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