A new glioblastoma cell trap for implantation after surgical resection

被引:27
作者
Autier, Lila [1 ,2 ,3 ]
Clavreul, Anne [1 ,2 ]
Cacicedo, Maximiliano L. [4 ]
Franconi, Florence [5 ,6 ]
Sindji, Laurence [2 ]
Rousseau, Audrey [2 ,7 ]
Perrot, Rodolphe [8 ]
Montero-Menei, Claudia N. [2 ]
Castro, Guillermo R. [4 ]
Menei, Philippe [1 ,2 ]
机构
[1] CHU, Dept Neurochirurg, 4 Rue Larrey, F-49933 Angers 9, France
[2] Univ Angers, Univ Nantes, INSERM, CRCINA, Angers, France
[3] CHU, Dept Neurol, Angers, France
[4] Univ Nacl La Plata, CONICET, CCT La Plata, Nanobiomat Lab,CINDEFI,Sch Sci, Buenos Aires, DF, Argentina
[5] Univ Angers, PRISM Icat, PRISM, Angers, France
[6] Univ Angers, CNRS UMR 6021, INSERM U1066, MINT,Micro & Nanomed Translat, Angers, France
[7] CHU, Lab Pathol Cellulaire & Tissulaire, Angers, France
[8] Univ Angers, SCIAM, Angers, France
关键词
Bacterial cellulose; Biomaterial; Cell trap; Glioblastoma; BACTERIAL CELLULOSE; ADJUVANT TEMOZOLOMIDE; TUMOR-CELLS; GLIOMA; RADIOTHERAPY; DELIVERY; MIGRATION; FILMS; BIOCOMPATIBILITY; NANOCELLULOSE;
D O I
10.1016/j.actbio.2018.11.027
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Glioblastoma (GB) is a highly infiltrative tumor, recurring, in 90% of cases, within a few centimeters of the surgical resection cavity, even with adjuvant chemo/radiotherapy. Residual GB cells left in the margins or infiltrating the brain parenchyma shelter behind the extremely fragile and sensitive brain tissue and may favor recurrence. Tools for eliminating these cells without damaging the brain microenvironment are urgently required. We propose a strategy involving the implantation, into the tumor bed after resection, of a scaffold to concentrate and trap these cells, to facilitate their destruction by targeted therapies, such as stereotactic radiosurgery. We used bacterial cellulose (BC), an easily synthesized and modifiable random nanofibrous biomaterial, to make the trap. We showed that the structure of BC membranes was ideal for trapping tumor cells and that BC implants were biocompatible with brain parenchyma. We also demonstrated the visibility of BC on magnetic resonance imaging, making it possible to follow its fate in clinical situations and to define the target volume for stereotactic radiosurgery more precisely. Furthermore, BC membranes can be loaded with chemoattractants, which were released and attracted tumor cells in vitro. This is of particular interest for trapping GB cells infiltrating tissues within a few centimeters of the resection cavity. Our data suggest that BC membranes could be a scaffold of choice for implantation after surgical resection to trap residual GB cells. Statement of Significance Glioblastoma is a highly infiltrative tumor, recurring, in 90% of cases, within a few centimeters of the surgical resection cavity, even with adjuvant chemo/radiotherapy. Residual tumor cells left in the margins or infiltrating the brain parenchyma shelter behind the extremely fragile and sensitive brain tissue and contribute to the risk of recurrence. Finding tools to eliminate these cells without damaging the brain microenvironment is a real challenge. We propose a strategy involving the implantation, into the walls of the surgical resection cavity, of a scaffold to concentrate and trap the residual tumor cells, to facilitate their destruction by targeted therapies, such as stereotactic radiosurgery. (C) 2018 Published by Elsevier Ltd on behalf of Acta Materialia Inc.
引用
收藏
页码:268 / 279
页数:12
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