Tumor Treating Fields (TTFields) Reversibly Permeabilize the Blood-Brain Barrier In Vitro and In Vivo

被引:35
作者
Salvador, Ellaine [1 ]
Kessler, Almuth F. [1 ]
Domroese, Dominik [1 ]
Hoermann, Julia [1 ]
Schaeffer, Clara [1 ]
Giniunaite, Aiste [1 ]
Burek, Malgorzata [2 ]
Tempel-Brami, Catherine [3 ]
Voloshin, Tali [3 ]
Volodin, Alexandra [3 ]
Zeidan, Adel [3 ]
Giladi, Moshe [3 ]
Ernestus, Ralf-Ingo [1 ]
Loehr, Mario [1 ]
Foerster, Carola Y. [2 ]
Hagemann, Carsten [1 ]
机构
[1] Univ Wurzburg, Dept Neurosurg, Sect Expt Neurosurg, D-97080 Wurzburg, Germany
[2] Univ Wurzburg, Dept Anaesthesiol Intens Care Emergency & Pain Me, D-97080 Wurzburg, Germany
[3] Novocure Ltd, IL-3190500 Haifa, Israel
关键词
blood-brain barrier; TTFields; CNS disorders; DRUG-DELIVERY; RHO-KINASE; ENDOTHELIAL-CELLS; TIGHT JUNCTIONS; PHASE-II; PACLITAXEL; CLAUDIN-5; CHEMOTHERAPY; DISRUPTION; GLIOBLASTOMA;
D O I
10.3390/biom12101348
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Despite the availability of numerous therapeutic substances that could potentially target CNS disorders, an inability of these agents to cross the restrictive blood-brain barrier (BBB) limits their clinical utility. Novel strategies to overcome the BBB are therefore needed to improve drug delivery. We report, for the first time, how Tumor Treating Fields (TTFields), approved for glioblastoma (GBM), affect the BBB's integrity and permeability. Here, we treated murine microvascular cerebellar endothelial cells (cerebEND) with 100-300 kHz TTFields for up to 72 h and analyzed the expression of barrier proteins by immunofluorescence staining and Western blot. In vivo, compounds normally unable to cross the BBB were traced in healthy rat brain following TTFields administration at 100 kHz. The effects were analyzed via MRI and immunohistochemical staining of tight-junction proteins. Furthermore, GBM tumor-bearing rats were treated with paclitaxel (PTX), a chemotherapeutic normally restricted by the BBB combined with TTFields at 100 kHz. The tumor volume was reduced with TTFields plus PTX, relative to either treatment alone. In vitro, we demonstrate that TTFields transiently disrupted BBB function at 100 kHz through a Rho kinase-mediated tight junction claudin-5 phosphorylation pathway. Altogether, if translated into clinical use, TTFields could represent a novel CNS drug delivery strategy.
引用
收藏
页数:20
相关论文
共 73 条
[1]   The blood-brain barrier: an overview - Structure, regulation, and clinical implications [J].
Ballabh, P ;
Braun, A ;
Nedergaard, M .
NEUROBIOLOGY OF DISEASE, 2004, 16 (01) :1-13
[2]   From blood-brain barrier to blood-brain interface: new opportunities for CNS drug delivery [J].
Banks, William A. .
NATURE REVIEWS DRUG DISCOVERY, 2016, 15 (04) :275-+
[3]   Driving Rho GTPase activity in endothelial cells regulates barrier integrity [J].
Beckers, Cora M. L. ;
van Hinsbergh, Victor W. M. ;
Amerongen, Geerten P. van Nieuw .
THROMBOSIS AND HAEMOSTASIS, 2010, 103 (01) :40-55
[4]  
Bonakdar M, 2017, RSC ADV, V7, P42811, DOI [10.1039/c7ra07603g, 10.1039/C7RA07603G]
[5]  
Brandes AA, 2000, ANTICANCER RES, V20, P1913
[6]   Generation of an Immortalized Murine Brain Microvascular Endothelial Cell Line as an In Vitro Blood Brain Barrier Model [J].
Burek, Malgorzata ;
Salvador, Ellaine ;
Foerster, Carola Y. .
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2012, (66)
[7]  
Chakraborty S, 2016, J EXP THER ONCOL, V11, P261
[8]  
Chang SM, 2001, CANCER, V91, P417, DOI 10.1002/1097-0142(20010115)91:2<417::AID-CNCR1016>3.0.CO
[9]  
2-9
[10]  
Choi JJ, 2005, ULTRASON, P988