Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/25541

TitleIn vitro and in vivo analysis of RTK inhibitor efficacy and identification of its novel targets in glioblastomas
Author(s)Martinho, Olga
Oliveira, Renato José Silva
Gonçalves, Vera M.
Clara, Carlos
Almeida, José Reynaldo
Carvalho, André Lopes
Barata, João Taborda
Reis, R. M.
Issue date4-Oct-2013
PublisherTransonc
JournalTranslational Oncology
Abstract(s)Treatment for glioblastoma consists of radiotherapy and temozolomide-based chemotherapy. However, virtually all patients recur, leading to a fatal outcome. Receptor tyrosine kinase (RTK)-targeted therapy has been the focus of attention in novel treatment options for these patients. Here, we compared the efficacy of imatinib, sunitinib, and cediranib in glioblastoma models. In the present work, the biologic effect of the drugs was screened by viability, cell cycle, apoptosis, migration, and invasion in vitro assays or in vivo by chick chorioallantoic membrane assay. Intracellular signaling was assessed by Western blot and the RTK targets were identified using phospho-RTK arrays. The amplified status of KIT, PDGFRA, and VEGFR2 genes was assessed by quantitative polymerase chain reaction. In a panel of 10 glioblastoma cell lines, we showed that cediranib was the most potent. In addition, cediranib and sunitinib synergistically sensitize the cells to temozolomide. Cediranib efficacy was shown to associate with higher cytostatic and unique cytotoxic effects in vitro and both antitumoral and antiangiogenic activity in vivo, which could associate with its great capacity to inhibit mitogen-activated protein kinase (MAPK) and AKT pathways. The molecular status of KIT, PDGFRA, and VEGFR2 did not predict glioblastoma cell responsiveness to any of the RTK inhibitors. Importantly, phospho-RTK arrays revealed novel targets for cediranib and sunitinib therapy. In conclusion, the novel targets found may be of value as future biomarkers for therapy response in glioblastoma and lead to the rational selection of patients for effective molecular targeted treatment.
TypeArticle
URIhttp://hdl.handle.net/1822/25541
DOI10.1593/tlo.12400
ISSN1936-5233
Publisher versionhttp://www.transonc.com/index.php
Peer-Reviewedyes
AccessOpen access
Appears in Collections:ICVS - Artigos em Revistas Internacionais com Referee

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