The effect of thermal therapy on the blood-brain barrier and blood-tumor barrier

References

• Langen UH, Ayloo S, Gu C. Development and cell biology of the blood-brain barrier. Annu Rev Cell Dev Biol. 2019;35:591–613.
   PubMed Web of Science ®Google Scholar
• Wen PY, Kesari S. Malignant gliomas in adults. N Engl J Med. 2008;359(5):492–507.
   PubMed Web of Science ®Google Scholar
• Thomsen MS, Routhe LJ, Moos T. The vascular basement membrane in the healthy and pathological brain. J Cereb Blood Flow Metab. 2017;37(10):3300–3317.
   PubMed Web of Science ®Google Scholar
• Rapoport SI. Osmotic opening of the blood–brain barrier: principles, mechanism, and therapeutic applications. Cell Mol Neurobiol. 2000;20(2):217–230.
   PubMed Web of Science ®Google Scholar
• Sandberg DI, Bilsky MH, Souweidane MM, et al. Ommaya reservoirs for the treatment of leptomeningeal metastases. Neurosurgery. 2000;47(1):49–54. discussion 54–45
   PubMed Web of Science ®Google Scholar
• Westphal M, Hilt DC, Bortey E, et al. A phase 3 trial of local chemotherapy with biodegradable carmustine (bcnu) wafers (gliadel wafers) in patients with primary malignant glioma. Neuro Oncol. 2003;5(2):79–88.
   PubMed Web of Science ®Google Scholar
• Menei P, Jadaud E, Faisant N, et al. Stereotaxic implantation of 5-fluorouracil-releasing microspheres in malignant glioma. Cancer. 2004;100(2):405–410.
   PubMed Web of Science ®Google Scholar
• Demeule M, Regina A, Che C, et al. Identification and design of peptides as a new drug delivery system for the brain. J Pharmacol Exp Ther. 2008;324(3):1064–1072.
   PubMed Web of Science ®Google Scholar
• Ren J, Shen S, Wang D, et al. The targeted delivery of anticancer drugs to brain glioma by pegylated oxidized multi-walled carbon nanotubes modified with angiopep-2. Biomaterials. 2012;33(11):3324–3333.
   PubMed Web of Science ®Google Scholar
• Leuthardt EC, Duan C, Kim MJ, et al. Hyperthermic laser ablation of recurrent glioblastoma leads to temporary disruption of the peritumoral blood brain barrier. PLoS One. 2016;11(2):e0148613
   PubMed Web of Science ®Google Scholar
• LaRiviere MJ, Gross RE. Stereotactic laser ablation for medically intractable epilepsy: the next generation of minimally invasive epilepsy surgery. Front Surg. 2016;3:64
   PubMed Web of Science ®Google Scholar
• Salehi A, Kamath AA, Leuthardt EC, et al. Management of intracranial metastatic disease with laser interstitial thermal therapy. Front Oncol. 2018;8:499.
   PubMed Web of Science ®Google Scholar
• Kamath AA, Friedman DD, Akbari SHA, et al. Glioblastoma treated with magnetic resonance imaging-guided laser interstitial thermal therapy: safety, efficacy, and outcomes. Neurosurgery. 2019;84(4):836–843.
   PubMed Web of Science ®Google Scholar
• Bown SG. Phototherapy in tumors. World J Surg. 1983;7(6):700–709.
   PubMed Web of Science ®Google Scholar
• De Poorter J, De Wagter C, De Deene Y, et al. Noninvasive mri thermometry with the proton resonance frequency (prf) method: in vivo results in human muscle. Magn Reson Med. 1995;33(1):74–81.
   PubMed Web of Science ®Google Scholar
• Abbott NJ, Patabendige AA, Dolman DE, et al. Structure and function of the blood-brain barrier. Neurobiol Dis. 2010;37(1):13–25.
   PubMed Web of Science ®Google Scholar
• O'Brown NM, Pfau SJ, Gu C. Bridging barriers: a comparative look at the blood-brain barrier across organisms. Genes Dev. 2018;32(7-8):466–478.
   PubMed Web of Science ®Google Scholar
• Wolburg H, Wolburg-Buchholz K, Kraus J, et al. Localization of claudin-3 in tight junctions of the blood-brain barrier is selectively lost during experimental autoimmune encephalomyelitis and human glioblastoma multiforme. Acta Neuropathol. 2003;105(6):586–592.
   PubMed Web of Science ®Google Scholar
• Hamm S, Dehouck B, Kraus J, et al. Astrocyte mediated modulation of blood-brain barrier permeability does not correlate with a loss of tight junction proteins from the cellular contacts. Cell Tissue Res. 2004;315(2):157–166.
   PubMed Web of Science ®Google Scholar
• Hawkins BT, Davis TP. The blood-brain barrier/neurovascular unit in health and disease. Pharmacol Rev. 2005;57(2):173–185.
   PubMed Web of Science ®Google Scholar
• Hamilton NB, Attwell D, Hall CN. Pericyte-mediated regulation of capillary diameter: a component of neurovascular coupling in health and disease. Front Neuroenergetics. 2010;2:5.
   PubMedGoogle Scholar
• Attwell D, Mishra A, Hall CN, et al. What is a pericyte? J Cereb Blood Flow Metab. 2016;36(2):451–455.
   PubMed Web of Science ®Google Scholar
• Vanlandewijck M, He L, Mae MA, et al. A molecular atlas of cell types and zonation in the brain vasculature. Nature. 2018;554(7693):475–480.
   PubMed Web of Science ®Google Scholar
• Daneman R, Zhou L, Kebede AA, et al. Pericytes are required for blood-brain barrier integrity during embryogenesis. Nature. 2010;468(7323):562–566.
   PubMed Web of Science ®Google Scholar
• Wong AD, Ye M, Levy AF, et al. The blood-brain barrier: an engineering perspective. Front Neuroeng. 2013;6:7
   PubMedGoogle Scholar
• Liu X, Tu M, Kelly RS, et al. Development of a computational approach to predict blood-brain barrier permeability. Drug Metab Dispos. 2004;32(1):132–139.
   PubMed Web of Science ®Google Scholar
• Nag S, Begley D. Blood-brain barrier, exchange of metabolites and gases. Pathol Genet. Cerebrovas Dise. 2005:22–29.
   Google Scholar
• Dallas S, Miller DS, Bendayan R. Multidrug resistance-associated proteins: expression and function in the central nervous system. Pharmacol Rev. 2006;58(2):140–161.
   PubMed Web of Science ®Google Scholar
• Zhao Z, Nelson AR, Betsholtz C, et al. Establishment and dysfunction of the blood-brain barrier. Cell. 2015;163(5):1064–1078.
   PubMed Web of Science ®Google Scholar
• Mohri M, Nitta H, Yamashita J. Expression of multidrug resistance-associated protein (mrp) in human gliomas. J Neurooncol. 2000;49(2):105–115.
   PubMed Web of Science ®Google Scholar
• Abe T, Mori T, Wakabayashi Y, et al. Expression of multidrug resistance protein gene in patients with glioma after chemotherapy. J Neurooncol. 1998;40(1):11–18.
   PubMed Web of Science ®Google Scholar
• Wolburg H, Wolburg-Buchholz K, Engelhardt B. Diapedesis of mononuclear cells across cerebral venules during experimental autoimmune encephalomyelitis leaves tight junctions intact. Acta Neuropathol. 2005;109(2):181–190.
   PubMed Web of Science ®Google Scholar
• Engelhardt B, Vajkoczy P, Weller RO. The movers and shapers in immune privilege of the cns. Nat Immunol. 2017;18(2):123–131.
   PubMed Web of Science ®Google Scholar
• Konsman JP, Drukarch B, Van Dam A-M. (Peri)vascular production and action of pro-inflammatory cytokines in brain pathology. Clin Sci. 2007;112(1):1–25.
   PubMed Web of Science ®Google Scholar
• Karman J, Ling CY, Sandor M, et al. Initiation of immune responses in brain is promoted by local dendritic cells. J Immunol. 2004;173(4):2353–2361.
   PubMed Web of Science ®Google Scholar
• Sarkaria JN, Hu LS, Parney IF, et al. Is the blood-brain barrier really disrupted in all glioblastomas? A critical assessment of existing clinical data. Neuro-oncology. 2018;20(2):184–191.
   PubMed Web of Science ®Google Scholar
• Achrol AS, Rennert RC, Anders C, et al. Brain metastases. Nat Rev Dis Primers. 2019;5(1):5
   PubMed Web of Science ®Google Scholar
• Watkins S, Robel S, Kimbrough IF, et al. Disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells. Nat Commun. 2014;5:4196
   PubMed Web of Science ®Google Scholar
• Liebner S, Fischmann A, Rascher G, et al. Claudin-1 and claudin-5 expression and tight junction morphology are altered in blood vessels of human glioblastoma multiforme. Acta Neuropathol. 2000;100(3):323–331.
   PubMed Web of Science ®Google Scholar
• Noell S, Ritz R, Wolburg-Buchholz K, et al. An allograft glioma model reveals the dependence of aquaporin-4 expression on the brain microenvironment. PLoS One. 2012;7(5):e36555
   PubMed Web of Science ®Google Scholar
• Jain RK, di Tomaso E, Duda DG, et al. Angiogenesis in brain tumours. Nat Rev Neurosci. 2007;8(8):610–622.
   PubMed Web of Science ®Google Scholar
• Quail DF, Joyce JA. The microenvironmental landscape of brain tumors. Cancer Cell. 2017;31(3):326–341.
   PubMed Web of Science ®Google Scholar
• Santarosa C, Castellano A, Conte GM, et al. Dynamic contrast-enhanced and dynamic susceptibility contrast perfusion mr imaging for glioma grading: preliminary comparison of vessel compartment and permeability parameters using hotspot and histogram analysis. Eur J Radiol. 2016;85(6):1147–1156.
   PubMed Web of Science ®Google Scholar
• Zhou W, Chen C, Shi Y, et al. Targeting glioma stem cell-derived pericytes disrupts the blood-tumor barrier and improves chemotherapeutic efficacy. Cell Stem Cell. 2017;21(5):591–603 e594.
   PubMed Web of Science ®Google Scholar
• Lyle LT, Lockman PR, Adkins CE, et al. Alterations in pericyte subpopulations are associated with elevated Blood-Tumor Barrier Permeability in Experimental Brain Metastasis of Breast Cancer. Clin Cancer Res. 2016;22(21):5287–5299.
   PubMed Web of Science ®Google Scholar
• Phoenix TN, Patmore DM, Boop S, et al. Medulloblastoma genotype dictates blood brain barrier phenotype. Cancer Cell. 2016;29(4):508–522.
   PubMed Web of Science ®Google Scholar
• Juillerat-Jeanneret L. The targeted delivery of cancer drugs across the blood-brain barrier: chemical modifications of drugs or drug-nanoparticles? Drug Discov Today. 2008;13(23–24):1099–1106.
   PubMed Web of Science ®Google Scholar
• la Fougere C, Suchorska B, Bartenstein P, et al. Molecular imaging of gliomas with pet: opportunities and limitations. Neuro-oncology. 2011;13(8):806–819.
   PubMed Web of Science ®Google Scholar
• Van Tellingen O, Yetkin-Arik B, De Gooijer M, et al. Overcoming the blood-brain tumor barrier for effective glioblastoma treatment. Drug Resist Updat. 2015;19:1–12.
   PubMed Web of Science ®Google Scholar
• Siegal T, Rubinstein R, Bokstein F, et al. In vivo assessment of the window of barrier opening after osmotic blood-brain barrier disruption in humans. J Neurosurg. 2000;92(4):599–605.
   PubMed Web of Science ®Google Scholar
• Gonzales-Portillo GS, Sanberg PR, Franzblau M, et al. Mannitol-enhanced delivery of stem cells and their growth factors across the blood-brain barrier. Cell Transplant. 2014;23(4–5):531–539.
   PubMed Web of Science ®Google Scholar
• Choi C, Kim HM, Shon J, et al. Additional increased effects of mannitol-temozolomide combined treatment on blood-brain barrier permeability. Biochem Biophys Res Commun. 2018;497(2):769–775.
   PubMed Web of Science ®Google Scholar
• Williams PC, Henner WD, Roman-Goldstein S, et al. Toxicity and efficacy of carboplatin and etoposide in conjunction with disruption of the blood-brain tumor barrier in the treatment of intracranial neoplasms. Neurosurgery. 1995;37(1):17–27. discussion 27–18
   PubMed Web of Science ®Google Scholar
• Hynynen K. Hyperthermia-induced drug delivery in humans. Nat Biomed Eng. 2018;2(9):637–639.
   PubMed Web of Science ®Google Scholar
• Abrahao A, Meng Y, Llinas M, et al. First-in-human trial of blood-brain barrier opening in amyotrophic lateral sclerosis using mr-guided focused ultrasound. Nat Commun. 2019;10(1):4373
   PubMed Web of Science ®Google Scholar
• Sboros V. Response of contrast agents to ultrasound. Adv Drug Deliv Rev. 2008;60(10):1117–1136.
   PubMed Web of Science ®Google Scholar
• Mitragotri S. Innovation - healing sound: the use of ultrasound in drug delivery and other therapeutic applications. Nat Rev Drug Discov. 2005;4(3):255–260.
   PubMed Web of Science ®Google Scholar
• Carpentier A, Canney M, Vignot A, et al. Clinical trial of blood-brain barrier disruption by pulsed ultrasound. Sci Transl Med. 2016;8:343re342.
   Web of Science ®Google Scholar
• Regina A, Demeule M, Tripathy S, et al. Ang4043, a novel brain-penetrant peptide-mab conjugate, is efficacious against her2-positive intracranial tumors in mice. Mol Cancer Ther. 2015;14(1):129–140.
   PubMed Web of Science ®Google Scholar
• Coley WB. The treatment of malignant tumors by repeated inoculations of erysipelas: with a report of ten original cases. 1. Am J Med Sci (1827–1924). 1893;105(5):487–510.
   Google Scholar
• Hahn GM. Potential for therapy of drugs and hyperthermia. Cancer Res. 1979;39(6 Pt 2):2264–2268.
   PubMed Web of Science ®Google Scholar
• Salcman M, Samaras GM. Hyperthermia for brain tumors: biophysical rationale. Neurosurgery. 1981;9(3):327–335.
   PubMed Web of Science ®Google Scholar
• Salcman M, Samaras GM. Interstitial microwave hyperthermia for brain tumors. Results of a phase-1 clinical trial. J Neurooncol. 1983;1(3):225–236.
   PubMedGoogle Scholar
• Rahmathulla G, Recinos PF, Kamian K, et al. Mri-guided laser interstitial thermal therapy in neuro-oncology: a review of its current clinical applications. Oncology. 2014;87(2):67–82.
   PubMed Web of Science ®Google Scholar
• Hawasli AH, Kim AH, Dunn GP, et al. Stereotactic laser ablation of high-grade gliomas. Neurosurg Focus. 2014;37(6):E1.
   PubMed Web of Science ®Google Scholar
• Mohammadi AM, Hawasli AH, Rodriguez A, et al. The role of laser interstitial thermal therapy in enhancing progression-free survival of difficult-to-access high-grade gliomas: a multicenter study. Cancer Med. 2014;3(4):971–979.
   PubMed Web of Science ®Google Scholar
• Hawasli AH, Ray WZ, Murphy RK, et al. Magnetic resonance imaging-guided focused laser interstitial thermal therapy for subinsular metastatic adenocarcinoma: technical case report. Oper Neurosurg. 2011;70:onsE332-onsE338.
   Google Scholar
• Torres-Reveron J, Tomasiewicz HC, Shetty A, et al. Stereotactic laser induced thermotherapy (litt): a novel treatment for brain lesions regrowing after radiosurgery. J Neurooncol. 2013;113(3):495–503.
   PubMed Web of Science ®Google Scholar
• Mohammadi AM, Schroeder JL. Laser interstitial thermal therapy in treatment of brain tumors-the NeuroBlate System. Expert Rev Med Devices. 2014;11(2):109–119.
   PubMed Web of Science ®Google Scholar
• Davalos D, Grutzendler J, Yang G, et al. Atp mediates rapid microglial response to local brain injury in vivo. Nat Neurosci. 2005;8(6):752–758.
   PubMed Web of Science ®Google Scholar
• Nishimura N, Schaffer CB, Friedman B, et al. Targeted insult to subsurface cortical blood vessels using ultrashort laser pulses: three models of stroke. Nat Methods. 2006;3(2):99–108.
   PubMed Web of Science ®Google Scholar
• Stafford RJ, Fuentes D, Elliott AA, et al. Laser-induced thermal therapy for tumor ablation. Crit Rev Biomed Eng. 2010;38(1):79–100.
   PubMedGoogle Scholar
• Pettigrew RT, Galt JM, Ludgate CM, et al. Circulatory and biochemical effects of whole body hyperthermia. Br J Surg. 1974;61(9):727–730.
   PubMed Web of Science ®Google Scholar
• Laidler KJ. The development of the arrhenius equation. J Chem Educ. 1984;61(6):494–498.
   Web of Science ®Google Scholar
• Pruitt R, Gamble A, Black K, et al. Complication avoidance in laser interstitial thermal therapy: lessons learned. J Neurosurg. 2017;126(4):1238–1245.
   PubMed Web of Science ®Google Scholar
• Salem U, Kumar VA, Madewell JE, et al. Neurosurgical applications of mri guided laser interstitial thermal therapy (litt). Cancer Imaging. 2019;19(1):65.
   PubMed Web of Science ®Google Scholar
• Patel P, Patel NV, Danish SF. Intracranial mr-guided laser-induced thermal therapy: single-center experience with the visualase thermal therapy system. J Neurosurg. 2016;125(4):853–860.
   PubMed Web of Science ®Google Scholar
• Allen IV. Cerebral changes in experimental heatstroke. Ir J Med Sci. 1964;465:413–422.
   PubMedGoogle Scholar
• Oscar KJ, Hawkins TD. Microwave alteration of the blood-brain barrier system of rats. Brain Res. 1977;126(2):281–293.
   PubMed Web of Science ®Google Scholar
• Urakawa M, Yamaguchi K, Tsuchida E, et al. Blood-brain barrier disturbance following localized hyperthermia in rats. Int J Hyperthermia. 1995;11(5):709–718.
   PubMed Web of Science ®Google Scholar
• Salehi A, Paturu MR, Patel B, et al. Therapeutic enhancement of blood-brain and blood-tumor barrier permeability by laser interstitial thermal therapy. Neuro Oncol Adv. 2020;2.
   PubMedGoogle Scholar
• Lee EJ, Fomenko A, Lozano AM. Magnetic resonance-guided focused Ultrasound: current status and future perspectives in thermal ablation and blood-brain barrier opening. J Korean Neurosurg Soc. 2019;62(1):10–26.
   PubMed Web of Science ®Google Scholar