Cargando…
Generation of Glioblastoma Patient-Derived Intracranial Xenografts for Preclinical Studies
Glioblastoma multiforme (GBM) is the most malignant primary brain cancer affecting adults. Therapeutic options for GBM have remained the same for over a decade with no significant improvement. Many therapies that are successful in culture have failed in patients, likely due to the complex microenvir...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403971/ https://www.ncbi.nlm.nih.gov/pubmed/32698368 http://dx.doi.org/10.3390/ijms21145113 |
_version_ | 1783567048234762240 |
---|---|
author | Kerstetter-Fogle, Amber E. Harris, Peggy L. R. Brady-Kalnay, Susann M. Sloan, Andrew E. |
author_facet | Kerstetter-Fogle, Amber E. Harris, Peggy L. R. Brady-Kalnay, Susann M. Sloan, Andrew E. |
author_sort | Kerstetter-Fogle, Amber E. |
collection | PubMed |
description | Glioblastoma multiforme (GBM) is the most malignant primary brain cancer affecting adults. Therapeutic options for GBM have remained the same for over a decade with no significant improvement. Many therapies that are successful in culture have failed in patients, likely due to the complex microenvironment in the brain, which has yet to be reproduced in any culture model. Furthermore, the high passage number of cultured cells and clonal selection fail to recapitulate the molecular and genomic signatures of GBM. We have established orthotopic patient-derived xenografts (PDX) from 37 GBM patients with human GBM. Of the 69 patient samples analyzed, we were successful in passaging 37 lines three or more generations (53.6%). After phenotypic characterization of the xenografted tumor tissue, two different growth patterns emerged highly invasive or localized. The phenotype was dependent on malignancy and previous treatment of the patient from which the xenograft was derived. Physiologically, mice exhibited symptoms more quickly with each subsequent passage, particularly in the localized tumors. Study of these physiologically relevant human xenografts in mice will enable therapeutic screenings in a microenvironment that more closely resembles GBM and may allow development of individualized patient models which may eventually be used for simulating treatment. |
format | Online Article Text |
id | pubmed-7403971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74039712020-08-11 Generation of Glioblastoma Patient-Derived Intracranial Xenografts for Preclinical Studies Kerstetter-Fogle, Amber E. Harris, Peggy L. R. Brady-Kalnay, Susann M. Sloan, Andrew E. Int J Mol Sci Article Glioblastoma multiforme (GBM) is the most malignant primary brain cancer affecting adults. Therapeutic options for GBM have remained the same for over a decade with no significant improvement. Many therapies that are successful in culture have failed in patients, likely due to the complex microenvironment in the brain, which has yet to be reproduced in any culture model. Furthermore, the high passage number of cultured cells and clonal selection fail to recapitulate the molecular and genomic signatures of GBM. We have established orthotopic patient-derived xenografts (PDX) from 37 GBM patients with human GBM. Of the 69 patient samples analyzed, we were successful in passaging 37 lines three or more generations (53.6%). After phenotypic characterization of the xenografted tumor tissue, two different growth patterns emerged highly invasive or localized. The phenotype was dependent on malignancy and previous treatment of the patient from which the xenograft was derived. Physiologically, mice exhibited symptoms more quickly with each subsequent passage, particularly in the localized tumors. Study of these physiologically relevant human xenografts in mice will enable therapeutic screenings in a microenvironment that more closely resembles GBM and may allow development of individualized patient models which may eventually be used for simulating treatment. MDPI 2020-07-20 /pmc/articles/PMC7403971/ /pubmed/32698368 http://dx.doi.org/10.3390/ijms21145113 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kerstetter-Fogle, Amber E. Harris, Peggy L. R. Brady-Kalnay, Susann M. Sloan, Andrew E. Generation of Glioblastoma Patient-Derived Intracranial Xenografts for Preclinical Studies |
title | Generation of Glioblastoma Patient-Derived Intracranial Xenografts for Preclinical Studies |
title_full | Generation of Glioblastoma Patient-Derived Intracranial Xenografts for Preclinical Studies |
title_fullStr | Generation of Glioblastoma Patient-Derived Intracranial Xenografts for Preclinical Studies |
title_full_unstemmed | Generation of Glioblastoma Patient-Derived Intracranial Xenografts for Preclinical Studies |
title_short | Generation of Glioblastoma Patient-Derived Intracranial Xenografts for Preclinical Studies |
title_sort | generation of glioblastoma patient-derived intracranial xenografts for preclinical studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403971/ https://www.ncbi.nlm.nih.gov/pubmed/32698368 http://dx.doi.org/10.3390/ijms21145113 |
work_keys_str_mv | AT kerstetterfogleambere generationofglioblastomapatientderivedintracranialxenograftsforpreclinicalstudies AT harrispeggylr generationofglioblastomapatientderivedintracranialxenograftsforpreclinicalstudies AT bradykalnaysusannm generationofglioblastomapatientderivedintracranialxenograftsforpreclinicalstudies AT sloanandrewe generationofglioblastomapatientderivedintracranialxenograftsforpreclinicalstudies |