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Rulseh, A.M.; Keller, J.; Klener, J.; Sroubek, J.; Dbaly, V.; Syrucek, M.; Tovarys, F.; Vymazal, J. |
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Title |
Long-term survival of patients suffering from glioblastoma multiforme treated with tumor-treating fields |
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Journal Article |
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Year |
2012 |
Publication |
World Journal of Surgical Oncology |
Abbreviated Journal |
World J Surg Oncol |
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10 |
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220 |
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Abstract |
Glioblastoma multiforme (GBM) is the most common and malignant primary intracranial tumor, and has a median survival of only 10 to 14 months with only 3 to 5% of patients surviving more than three years. Recurrence (RGBM) is nearly universal, and further decreases the median survival to only five to seven months with optimal therapy. Tumor-treating fields (TTField) therapy is a novel treatment technique that has recently received CE and FDA approval for the treatment of RGBM, and is based on the principle that low intensity, intermediate frequency electric fields (100 to 300 kHz) may induce apoptosis in specific cell types. Our center was the first to apply TTField treatment to histologically proven GBM in a small pilot study of 20 individuals in 2004 and 2005, and four of those original 20 patients are still alive today. We report two cases of GBM and two cases of RGBM treated by TTField therapy, all in good health and no longer receiving any treatment more than seven years after initiating TTField therapy, with no clinical or radiological evidence of recurrence. |
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Department of Radiology, Na Homolce Hospital, Prague, Czech Republic |
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1477-7819 |
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PMID:23095807 |
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no |
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Call Number |
IT'IS @ evaj @ |
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391 |
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Antonini, R.A.; Benfante, R.; Gotti, C.; Moretti, M.; Kuster, N.; Schuderer, J.; Clementi, F.; Fornasari, D. |
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Title |
Extremely low-frequency electromagnetic field (ELF-EMF) does not affect the expression of alpha3, alpha5 and alpha7 nicotinic receptor subunit genes in SH-SY5Y neuroblastoma cell line |
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Journal Article |
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Year |
2006 |
Publication |
Toxicology Letters |
Abbreviated Journal |
Toxicol Lett |
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164 |
Issue |
3 |
Pages |
268-277 |
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Keywords |
Bicyclo Compounds, Heterocyclic/pharmacology; Blotting, Northern; Bungarotoxins/pharmacology; Cell Line, Tumor; Electromagnetic Fields/*adverse effects; Gene Expression/*radiation effects; Humans; Nerve Tissue Proteins/*genetics/metabolism; Neuroblastoma/pathology; Pyridines/pharmacology; RNA, Messenger/genetics; Radioligand Assay; Receptors, Nicotinic/*genetics/metabolism |
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Neuronal nicotinic acetylcholine receptors (nAChRs) are involved in a number of functional processes, including cognition, learning and memory, and alterations in their expression and/or activity have been implicated in various neurological disorders such as Alzheimer's disease (AD), Parkinson's disease and schizophrenia. Epidemiological studies have shown that exposure to electromagnetic fields (EMF) may contribute to the pathogenesis of neurodegenerative diseases such as Alzheimer's disease. Given the role of nAChRs in physiological and pathological conditions, we wondered whether an extremely low-frequency electromagnetic field (ELF-EMF) may affect the expression of the molecules involved in neurodegenerative processes. In order to investigate this possibility, we studied the expression of alpha3, alpha5 and alpha7 nicotinic subunits upon exposure of the SH-SY5Y human neuroblastoma cell line to a 50 Hz power-line magnetic field in a “blind trial” system; various magnetic flux densities and exposure times were applied. Our studies show that the expression of some relevant components of the cholinergic nicotinic system, which is one of the most affected neurotransmission systems in AD, did not undergo any change at molecular level by environmental exposure to ELF-EMF. |
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Department of Pharmacology, School of Medicine, University of Milan, via Vanvitelli 32, 20129 Milan, Italy |
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0378-4274 |
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PMID:16513298 |
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ITIS @ murbach @ |
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163 |
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Benfante, R.; Antonini, R.A.; Kuster, N.; Schuderer, J.; Maercker, C.; Adlkofer, F.; Clementi, F.; Fornasari, D. |
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The expression of PHOX2A, PHOX2B and of their target gene dopamine-beta-hydroxylase (DbetaH) is not modified by exposure to extremely-low-frequency electromagnetic field (ELF-EMF) in a human neuronal model |
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Journal Article |
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2008 |
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Toxicology in Vitro : an International Journal Published in Association With BIBRA |
Abbreviated Journal |
Toxicol In Vitro |
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22 |
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6 |
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1489-1495 |
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Cell Line, Tumor; Dopamine beta-Hydroxylase/radiation effects; Electromagnetic Fields/*adverse effects; Gene Expression/*radiation effects; Homeodomain Proteins/*radiation effects; Humans; Neuroblastoma/metabolism; Time Factors; Transcription Factors/*radiation effects; Transcription, Genetic/radiation effects; Tretinoin/pharmacology |
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The homeodomain transcription factors PHOX2A and PHOX2B are vital for development of the autonomic nervous system. Their spatial and temporal expression at the neural crest is instrumental in determining neuronal precursor fate, and by regulating DbetaH expression, the enzyme catalysing noradrenaline synthesis from dopamine, they also play a role in determination of noradrenergic phenotype. Disturbing this finely regulated process leads to disruption of autonomic development and autonomic dysfunction syndromes such as DbetaH deficiency. As it had previously been shown that the catecholamine system is responsive to ELF-EMF, and as this has also been linked to various pathologies and to certain types of cancer, we wondered whether exposure to this type of radiation could affect the expression of PHOX2A, PHOX2B and DbetaH, also during differentiation triggered by retinoic acid. To investigate this possibility we exposed the human SH-SY5Y neuroblastoma cell line to 50 Hz power-line magnetic field at various flux densities and for various exposure times. We measured gene expression in exposed cells compared to control cells and also investigated any changes at protein level. Using our exposure protocol, we found no changes at either transcript or protein level of these important components of the autonomic nervous system and catecholaminergic system. |
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Department of Pharmacology, School of Medicine, University of Milan, via Vanvitelli 32, Milan, Italy |
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0887-2333 |
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PMID:18572378 |
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ITIS @ murbach @ |
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164 |
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Bas, O.; Odaci, E.; Mollaoglu, H.; Ucok, K.; Kaplan, S. |
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Title |
Chronic prenatal exposure to the 900 megahertz electromagnetic field induces pyramidal cell loss in the hippocampus of newborn rats |
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Journal Article |
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2009 |
Publication |
Toxicology and Industrial Health |
Abbreviated Journal |
Toxicology and Industrial Health |
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25 |
Issue |
6 |
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377-384 |
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0748-2337 |
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CBM.UAM @ ccobaleda @ |
Serial |
474 |
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Author |
Zhu, H.; Wang, J.; Cui, J.; Fan, X. |
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Title |
Effects of extremely low frequency electromagnetic fields on human fetal scleral fibroblasts |
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Journal Article |
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Year |
2014 |
Publication |
Toxicology and industrial health |
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August |
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Keywords |
collagen type i; extremely low frequency electromagnetic; fibroblast; field; matrix metalloproteinase-2; sclera; transforming growth factor beta-2 |
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Abstract |
This study investigated the effects of extremely low frequency electromagnetic fields (ELF-EMFs) on human fetal scleral fibroblasts (HFSFs). HFSFs were subjected to 50 Hz artificial ELF-EMFs generated by Helmholtz coils with 0.1, 0.2, 0.5, and 1.0 mT field intensities for 6 to 48 h. The viability and factors involved in scleral structuring of HFSFs were determined. The growth rate of HFSFs significantly decreased after only 24 h of exposure to ELF-EMFs (0.2 mT). The messenger RNA (mRNA) expression of collagen type I (COL1A1) decreased and expression of matrix metalloproteinase-2 (MMP-2) increased significantly. There was a decrease in tissue inhibitor of MMP-2 mRNA levels between treated and control cells only at the 1.0 mT intensity level. Transforming growth factor beta-2 mRNA increased in exposed cells, and, simultaneously, fibroblast growth factor-2 mRNA levels decreased. The protein expressions of COL1A1 and MMP-2 were also significantly altered subsequent to exposure (p < 0.05). This study shows that ELF-EMFs had biological effects on HFSFs and could cause abnormality in scleral collagen. |
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WP5 In vitro |
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Call Number |
UNIBAS @ david.schuermann @ |
Serial |
629 |
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