INTRODUCTION: GBM stem cells are resistant to conventional treatment forming recurrent-tumors via angiogenesis. Thus, they are considered primary targets for novel therapeutic strategies for GBM. METHODS: We obtain relapsed chemo-radioresistant GBM stem cells overexpressing CD133 from which we develop a GBM model that we treat with immunotargeted pegylated silver nanobots(PEG-AgNPs) which are covalently conjugated to anti-CD133 MAbs for targeting Brain-Cancer-Stem-Cells (BCSCs) after receptor-mediated-endocytosis. Then, we treat them with radiofrequency-dielectric-heating (RFDH) as a novel postsurgical-adjuvant-treatment. RESULTS: Post-treatment, the silver nanobots AgNPs release Ag+ ions which disrupt mitochondrial-respiratory-chain(MRC) blocking ATP-synthesis by production of ROS which damage the DNA of CSCs leading to cell-cycle arrest at G2/M phase and type-1 PCD of stage-D2 or apoptosis. The capacitive nonionizing radiofrequency-dielectric-heating of 13.56MHz exerts hyperthermic cytotoxicity increasing the intracellular-Temperature of BCSCs up to 50 degrees Celcius leading to the necrosis of Brain-Cancer-Stem-Cells(BCSCs). CONCLUSION: This immunotargeted molecular robotic nanosurgical approach may be used as an adjuvant treatment against GBM which is resistant to conventional chemo/radiation therapy by eradicating its cancer-stem-cells.
. 2015 Apr 21;17(Suppl 3):iii40. doi: 10.1093/neuonc/nov061.162
TR-17: IMMUNOTARGETED-MOLECULAR-ROBOTIC-NANOSURGERY (ITMRN) ERADICATES GBM STEM-CELLS WITH RADIOFREQUENCY DIELECTRIC HEATING (RFDH) MEDIATED VIA SILVER-IMMUNONANOBOTS LINKED WITH anti-CD133 MAbs
John Giannios
1
John Giannios
1Int Soc of Molecular and Genomic Medicine and Int Assoc of Perioperative Medicine and Nanosurgery, Athens, Greece
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1Int Soc of Molecular and Genomic Medicine and Int Assoc of Perioperative Medicine and Nanosurgery, Athens, Greece
Issue date 2015 Jun.
© The Author(s) 2015. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
PMCID: PMC4482952
