Εμφάνιση απλής εγγραφής

dc.creatorDionigi L., Ragonese F., Monarca L., Covino S., de Luca A., Iannitti R.G., Bastioli F., Moulas A.N., Allegretti M., Fioretti B.en
dc.date.accessioned2023-01-31T07:57:07Z
dc.date.available2023-01-31T07:57:07Z
dc.date.issued2020
dc.identifier10.2174/1381612826666200401085634
dc.identifier.issn13816128
dc.identifier.urihttp://hdl.handle.net/11615/73373
dc.description.abstractGlioblastoma (GB) represents the most common and malignant form of glioma cancer. The Gold Standard in Glioblastoma is neurosurgical tumor removal and radiotherapy treatment in concomitant with temo-zolomide (TMZ). Unfortunately, because of tumor chemo and radio-resistance during this therapy, the patient’s outcome remains very poor, with a median overall survival of about 14.6 months. Resveratrol is a natural polyphenol with a stilbene structure with chemopreventive and anticancer properties. In the present review, we evaluated data from preclinical studies conducted with resveratrol as a possible adjuvant during the standard protocol of GB. Resveratrol can reach the brain parenchyma at sub-micromolar concentrations when administrated through conventional routes. In this way, resveratrol reduces cell invasion and increases the efficacy of radiotherapy (ra-diosensitizer effects) and temozolomide. The molecular mechanism of the adjuvant action of resveratrol may depend upon the reduction of PI3K/AKT/NF-κB axis and downstream targets O-6-methylguanine-DNA methyl-transferase (MGMT) and metalloproteinase-2 (MMP-2). It has been reported that redox signaling plays an important role in the regulation of autophagy. Resveratrol administration by External Carotid Artery (ECA) injection or by Lumbar Puncture (LP) can reach micromolar concentrations in tumor mass where it would inhibit tumor growth by STAT-3 dependent mechanisms. Preclinical evidences indicate a positive effect on the use of resvera-trol as an adjuvant in anti-GB therapy. Ameliorated formulations of resveratrol with a favorable plasmatic profile for a better brain distribution and timing sequences during radio and chemotherapy could represent a critical aspect for resveratrol use as an adjuvant for a clinical evaluation. © 2020 Bentham Science Publishers.en
dc.language.isoenen
dc.sourceCurrent Pharmaceutical Designen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85083730073&doi=10.2174%2f1381612826666200401085634&partnerID=40&md5=d276aa2efc574d0ddb3e741ae401ac5e
dc.subjectgelatinase Aen
dc.subjectimmunoglobulin enhancer binding proteinen
dc.subjectmethylated DNA protein cysteine methyltransferaseen
dc.subjectphosphatidylinositol 3 kinaseen
dc.subjectprotein kinase Ben
dc.subjectradiosensitizing agenten
dc.subjectresveratrolen
dc.subjectSTAT3 proteinen
dc.subjecttemozolomideen
dc.subjectalkylating agenten
dc.subjectgelatinase Aen
dc.subjectphosphatidylinositol 3 kinaseen
dc.subjectresveratrolen
dc.subjectadjuvant chemotherapyen
dc.subjectantineoplastic activityen
dc.subjectantiproliferative activityen
dc.subjectautophagy (cellular)en
dc.subjectbrain regionen
dc.subjectcancer inhibitionen
dc.subjectcancer radiotherapyen
dc.subjectcell invasionen
dc.subjectdrug distributionen
dc.subjectdrug effecten
dc.subjectdrug mechanismen
dc.subjectexternal carotid arteryen
dc.subjectglioblastomaen
dc.subjecthumanen
dc.subjectlumbar punctureen
dc.subjectnonhumanen
dc.subjectpreclinical studyen
dc.subjectpriority journalen
dc.subjectReviewen
dc.subjectsignal transductionen
dc.subjectsynergistic effecten
dc.subjecttumor volumeen
dc.subjectbrain tumoren
dc.subjectglioblastomaen
dc.subjectAntineoplastic Agents, Alkylatingen
dc.subjectBrain Neoplasmsen
dc.subjectGlioblastomaen
dc.subjectHumansen
dc.subjectMatrix Metalloproteinase 2en
dc.subjectPhosphatidylinositol 3-Kinasesen
dc.subjectResveratrolen
dc.subjectBentham Science Publishersen
dc.titleFocus on the use of resveratrol as an adjuvant in glioblastoma therapyen
dc.typeotheren


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