RT Journal Article
SR Electronic
T1 Efficacy of Combination Therapy with MET and VEGF Inhibitors for MET-overexpressing Glioblastoma
JF Anticancer Research
JO Anticancer Res
FD International Institute of Anticancer Research
SP 3871
OP 3876
VO 37
IS 7
A1 TAKESHI OKUDA
A1 TAKAYUKI TASAKI
A1 SUSUMU NAKATA
A1 KIMIHIRO YAMASHITA
A1 HIROMASA YOSHIOKA
A1 SHUICHI IZUMOTO
A1 AMAMI KATO
A1 MITSUGU FUJITA
YR 2017
UL http://ar.iiarjournals.org/content/37/7/3871.abstract
AB Background: Glioblastoma multiforme (GBM) is a malignant brain tumor with an extremely poor prognosis. GBM tissues frequently express mesenchymal–epithelial transition factor (MET), which induces cell division, growth and migration. In addition, angiogenesis is a significant feature of GBM, attributable to the overexpression of vascular endothelial growth factor (VEGF). Although the VEGF inhibitor bevacizumab was recently highlighted as the second-line drug for GBM treatment, GBMs often recur even with bevacizumab therapy. Based on these findings, we hypothesized that inhibition of both MET and VEGF would exhibit a synergistic effect on MET-overexpressing GBM. Materials and Methods: As we observed MET expression at high levels in some patients with GBM, we designed GL261 murine glioma-based experiments. GL261 cells were transfected with siRNAs specific for MET and VEGF in vitro, and the cell growth ratios were evaluated. Simultaneously, transfected GL261 cells were transplanted into the brain of C57BL/6 mice, and their survival was monitored. Results: GBM tissues frequently overexpressed MET protein at high levels compared with lower-grade gliomas. These GBMs at first responded to bevacizumab, but often eventually recurred. When GL261 cells were co-transfected with both MET-specific siRNA and VEGF-specific siRNA, the in vitro tumor cell growth significantly decelerated compared to single siRNA transfection. Consistently, when mice were transplanted with co-transfected GL261 cells, their survival was significantly prolonged compared to those given cells transfected with single siRNA. Conclusion: The current data indicate that the inhibition of both MET and VEGF exhibits efficient therapeutic effects of GBM-bearing hosts.