Cellular and molecular features related to exceptional therapy response and extreme long‐term survival in glioblastoma

Abstract Glioblastoma Multiforme (GBM) remains the most common malignant primary brain tumor with a dismal prognosis that rarely exceeds beyond 2 years despite extensive therapy, which consists of maximal safe surgical resection, radiotherapy, and/or chemotherapy. Recently, it has become clear that...

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Main Authors: B. Decraene, M. Vanmechelen, P. Clement, J. F. Daisne, I. Vanden Bempt, R. Sciot, A. D. Garg, P. Agostinis, F. De Smet, S. De Vleeschouwer
Format: Article
Language:English
Published: Wiley 2023-05-01
Series:Cancer Medicine
Subjects:
Online Access:https://doi.org/10.1002/cam4.5681
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author B. Decraene
M. Vanmechelen
P. Clement
J. F. Daisne
I. Vanden Bempt
R. Sciot
A. D. Garg
P. Agostinis
F. De Smet
S. De Vleeschouwer
author_facet B. Decraene
M. Vanmechelen
P. Clement
J. F. Daisne
I. Vanden Bempt
R. Sciot
A. D. Garg
P. Agostinis
F. De Smet
S. De Vleeschouwer
author_sort B. Decraene
collection DOAJ
description Abstract Glioblastoma Multiforme (GBM) remains the most common malignant primary brain tumor with a dismal prognosis that rarely exceeds beyond 2 years despite extensive therapy, which consists of maximal safe surgical resection, radiotherapy, and/or chemotherapy. Recently, it has become clear that GBM is not one homogeneous entity and that both intra‐and intertumoral heterogeneity contributes significantly to differences in tumoral behavior which may consequently be responsible for differences in survival. Strikingly and in spite of its dismal prognosis, small fractions of GBM patients seem to display extremely long survival, defined as surviving over 10 years after diagnosis, compared to the large majority of patients. Although the underlying mechanisms for this peculiarity remain largely unknown, emerging data suggest that still poorly characterized both cellular and molecular factors of the tumor microenvironment and their interplay probably play an important role. We hereby give an extensive overview of what is yet known about these cellular and molecular features shaping extreme long survival in GBM.
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spelling doaj.art-1525ca1bfd33402981e57cde4949d51c2023-06-06T07:30:47ZengWileyCancer Medicine2045-76342023-05-011210111071112610.1002/cam4.5681Cellular and molecular features related to exceptional therapy response and extreme long‐term survival in glioblastomaB. Decraene0M. Vanmechelen1P. Clement2J. F. Daisne3I. Vanden Bempt4R. Sciot5A. D. Garg6P. Agostinis7F. De Smet8S. De Vleeschouwer9KU Leuven, Laboratory for Precision Cancer Medicine Translational Cell and Tissue Research Unit Leuven BelgiumKU Leuven, Laboratory for Precision Cancer Medicine Translational Cell and Tissue Research Unit Leuven BelgiumDepartment of General Medical Oncology University Hospitals Leuven Leuven BelgiumRadiation Oncology Department University Hospitals Leuven Leuven BelgiumDepartment of Human Genetics University Hospitals Leuven Leuven BelgiumDepartment of Pathology University Hospitals Leuven Leuven BelgiumKU Leuven, Laboratory of Cell Stress & Immunity (CSI), Department of Cellular & Molecular Medicine Leuven BelgiumCell Death Research and Therapy Group Department of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, 3000 Leuven, Belgium VIB Center for Cancer Biology, 3000 Leuven BelgiumKU Leuven, Laboratory for Precision Cancer Medicine Translational Cell and Tissue Research Unit Leuven BelgiumKU Leuven Department of Neurosciences Experimental Neurosurgery and Neuroanatomy Research Group Leuven BelgiumAbstract Glioblastoma Multiforme (GBM) remains the most common malignant primary brain tumor with a dismal prognosis that rarely exceeds beyond 2 years despite extensive therapy, which consists of maximal safe surgical resection, radiotherapy, and/or chemotherapy. Recently, it has become clear that GBM is not one homogeneous entity and that both intra‐and intertumoral heterogeneity contributes significantly to differences in tumoral behavior which may consequently be responsible for differences in survival. Strikingly and in spite of its dismal prognosis, small fractions of GBM patients seem to display extremely long survival, defined as surviving over 10 years after diagnosis, compared to the large majority of patients. Although the underlying mechanisms for this peculiarity remain largely unknown, emerging data suggest that still poorly characterized both cellular and molecular factors of the tumor microenvironment and their interplay probably play an important role. We hereby give an extensive overview of what is yet known about these cellular and molecular features shaping extreme long survival in GBM.https://doi.org/10.1002/cam4.5681gbmglioblastomalong‐term survivorsmolecular markers
spellingShingle B. Decraene
M. Vanmechelen
P. Clement
J. F. Daisne
I. Vanden Bempt
R. Sciot
A. D. Garg
P. Agostinis
F. De Smet
S. De Vleeschouwer
Cellular and molecular features related to exceptional therapy response and extreme long‐term survival in glioblastoma
Cancer Medicine
gbm
glioblastoma
long‐term survivors
molecular markers
title Cellular and molecular features related to exceptional therapy response and extreme long‐term survival in glioblastoma
title_full Cellular and molecular features related to exceptional therapy response and extreme long‐term survival in glioblastoma
title_fullStr Cellular and molecular features related to exceptional therapy response and extreme long‐term survival in glioblastoma
title_full_unstemmed Cellular and molecular features related to exceptional therapy response and extreme long‐term survival in glioblastoma
title_short Cellular and molecular features related to exceptional therapy response and extreme long‐term survival in glioblastoma
title_sort cellular and molecular features related to exceptional therapy response and extreme long term survival in glioblastoma
topic gbm
glioblastoma
long‐term survivors
molecular markers
url https://doi.org/10.1002/cam4.5681
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