Patient-derived Tumor Models for Diffuse Intrinsic Pontine Gliomas

Background: Diffuse intrinsic pontine gliomas represent a unique subtype of primary brain tumors occuring in a specific location and age. Their growth demonstrates early invasion and, following diagnosis, rapid growth not responsive to common therapies. Until recently, the genetic and cellular basis...

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Bibliographic Details
Published in:Current neuropharmacology 2017-01, Vol.15 (1), p.98-103
Main Authors: Hashizume, Rintaro, Gupta, Nalin
Format: Article
Language:English
Subjects:
Animal models
Animals
Brain cancer
Brain Stem Neoplasms - pathology
Brain Stem Neoplasms - therapy
Brain tumors
Glioma
Glioma - pathology
Glioma - therapy
Humans
Latency
Mutation
Pons - pathology
Transplantation, Heterologous
Tumors
Xenografts
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Summary:Background: Diffuse intrinsic pontine gliomas represent a unique subtype of primary brain tumors occuring in a specific location and age. Their growth demonstrates early invasion and, following diagnosis, rapid growth not responsive to common therapies. Until recently, the genetic and cellular basis of these tumors was unknown. Genetic evidence implicates mutations in the histone genes in the origin of these tumors. Methods: Surgical biopsies performed on selected patients have resulted in the establishment of anatomically accurate mouse models that have been used to examine patterns of growth and response to new therapeutic agents. Results: Human derived pontine glioma models recapitulate the invasive patterns of growth. The grade of the original tumor affects the latency of tumor growth after implantation. Conclusion: The use of human-derived xenograft models allows for improved pre-clinical testing of new therapeutic targets in a tumor- and organ-specific manner.
ISSN:1570-159X
1875-6190
DOI:10.2174/1570159X14666160523144117