Implementation of a multi-institutional diffuse intrinsic pontine glioma autopsy protocol and characterization of a primary cell culture

被引:22
作者
Caretti, V. [1 ,2 ,3 ]
Jansen, M. H. A. [1 ,3 ]
van Vuurden, D. G. [1 ,3 ]
Lagerweij, T. [1 ,2 ,3 ]
Bugiani, M. [4 ]
Horsman, I. [5 ]
Wessels, H. [5 ]
van der Valk, P. [4 ]
Cloos, J. [1 ]
Noske, D. P. [2 ,3 ]
Vandertop, W. P. [2 ]
Wesseling, P. [4 ,6 ]
Wurdinger, T. [2 ,3 ,7 ,8 ]
Hulleman, E. [1 ,3 ]
Kaspers, G. J. L. [1 ]
机构
[1] Vrije Univ Amsterdam, Med Ctr, Dept Pediat Oncol, NL-1081 HZ Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Med Ctr, Neurosurg Ctr Amsterdam, NL-1081 HZ Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr, Neurooncol Res Grp, NL-1081 HZ Amsterdam, Netherlands
[4] Vrije Univ Amsterdam, Med Ctr, Dept Pathol, NL-1081 HZ Amsterdam, Netherlands
[5] Vrije Univ Amsterdam, Med Ctr, Dept Clin Genet, NL-1081 HZ Amsterdam, Netherlands
[6] Radboud Univ Nijmegen, Med Ctr, Dept Pathol, NL-6525 ED Nijmegen, Netherlands
[7] Massachusetts Gen Hosp, Dept Neurol, Mol Neurogenet Unit, Boston, MA 02114 USA
[8] Harvard Univ, Sch Med, Boston, MA USA
关键词
autopsy; brain neoplasms; brainstem neoplasms; cells cultured; disease models animal; pontine glioma; STEREOTACTIC BIOPSY; CLINICAL-TRIALS; IN-VIVO; CHILDREN; TUMORS; LINES; GLIOBLASTOMAS; CHILDHOOD; MODELS; GROWTH;
D O I
10.1111/j.1365-2990.2012.01294.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
V. Caretti, M. H. A. Jansen, D. G. van Vuurden, T. Lagerweij, M. Bugiani, I. Horsman, H. Wessels, P. van der Valk, J. Cloos, D. P. Noske, W. P. Vandertop, P. Wesseling, T. Wurdinger, E. Hulleman and G. J. L. Kaspers (2013) Neuropathology and Applied Neurobiology39, 426436 Implementation of a multi-institutional diffuse intrinsic pontine glioma autopsy protocol and characterization of a primary cell culture Aims: Diffuse intrinsic pontine glioma (DIPG) is a fatal paediatric malignancy. Tumour resection is not possible without serious morbidity and biopsies are rarely performed. The resulting lack of primary DIPG material has made preclinical research practically impossible and has hindered the development of new therapies for this disease. The aim of the current study was to address the lack of primary DIPG material and preclinical models by developing a multi-institutional autopsy protocol. Methods: An autopsy protocol was implemented in the Netherlands to obtain tumour material within a brief post mortem interval. A team of neuropathologists and researchers was available at any time to perform the autopsy and process the material harvested. Whole brain autopsy was performed and primary DIPG material and healthy tissue were collected from all affected brain areas. Finally, the study included systematic evaluation by parents. Results: Five autopsies were performed. The mean time interval between death and time of autopsy was 3h (range 24). All tumours were graded as glioblastoma. None of the parents regretted their choice to participate, and they all derived comfort in donating tissue of their child in the hope to help future DIPG patients. In addition, we developed and characterized one of the first DIPG cell cultures from post mortem material. Conclusion: Here we show that obtaining post mortem DIPG tumour tissue for research purposes is feasible with short delay, and that the autopsy procedure is satisfying for participating parents and can be suitable for the development of preclinical DIPG models.
引用
收藏
页码:426 / 436
页数:11
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