[HTML][HTML] The tumor microenvironment strongly impacts master transcriptional regulators and gene expression class of glioblastoma
The Cancer Genome Atlas (TCGA) project has generated gene expression data that divides
glioblastoma (GBM) into four transcriptional classes: proneural, neural, classical, and …
glioblastoma (GBM) into four transcriptional classes: proneural, neural, classical, and …
[PDF][PDF] Transcriptome analysis reveals tumor microenvironment changes in glioblastoma
Y Hoogstrate, K Draaisma, SA Ghisai, L van Hijfte… - Cancer Cell, 2023 - cell.com
A better understanding of transcriptional evolution of IDH-wild-type glioblastoma may be
crucial for treatment optimization. Here, we perform RNA sequencing (RNA-seq)(n= 322 test …
crucial for treatment optimization. Here, we perform RNA sequencing (RNA-seq)(n= 322 test …
Gene expression profiling reveals molecularly and clinically distinct subtypes of glioblastoma multiforme
Y Liang, M Diehn, N Watson… - Proceedings of the …, 2005 - National Acad Sciences
Glioblastoma multiforme (GBM) is the most common form of malignant glioma, characterized
by genetic instability, intratumoral histopathological variability, and unpredictable clinical …
by genetic instability, intratumoral histopathological variability, and unpredictable clinical …
An anatomic transcriptional atlas of human glioblastoma
Glioblastoma is an aggressive brain tumor that carries a poor prognosis. The tumor's
molecular and cellular landscapes are complex, and their relationships to histologic features …
molecular and cellular landscapes are complex, and their relationships to histologic features …
[HTML][HTML] Novel genotype-phenotype associations in human cancers enabled by advanced molecular platforms and computational analysis of whole slide images
Technological advances in computing, imaging, and genomics have created new
opportunities for exploring relationships between histology, molecular events, and clinical …
opportunities for exploring relationships between histology, molecular events, and clinical …
[HTML][HTML] Molecular and genomic alterations in glioblastoma multiforme
I Crespo, AL Vital, M Gonzalez-Tablas… - The American journal of …, 2015 - Elsevier
In recent years, important advances have been achieved in the understanding of the
molecular biology of glioblastoma multiforme (GBM); thus, complex genetic alterations and …
molecular biology of glioblastoma multiforme (GBM); thus, complex genetic alterations and …
Molecular heterogeneity of glioblastoma and its clinical relevance
K Eder, B Kalman - Pathology & Oncology Research, 2014 - Springer
Glioblastoma is the most common intracranial malignancy and constitutes about 50% of all
gliomas. Both inter-tumor and intra-tumor histological heterogeneity had been recognized by …
gliomas. Both inter-tumor and intra-tumor histological heterogeneity had been recognized by …
[HTML][HTML] Molecular crosstalk between tumour and brain parenchyma instructs histopathological features in glioblastoma
The histopathological and molecular heterogeneity of glioblastomas represents a major
obstacle for effective therapies. Glioblastomas do not develop autonomously, but evolve in a …
obstacle for effective therapies. Glioblastomas do not develop autonomously, but evolve in a …
[PDF][PDF] Glioma progression is shaped by genetic evolution and microenvironment interactions
The factors driving therapy resistance in diffuse glioma remain poorly understood. To identify
treatment-associated cellular and genetic changes, we analyzed RNA and/or DNA …
treatment-associated cellular and genetic changes, we analyzed RNA and/or DNA …
Identification of prognostic gene signatures of glioblastoma: a study based on TCGA data analysis
YW Kim, D Koul, SH Kim, AK Lucio-Eterovic… - Neuro …, 2013 - academic.oup.com
Abstract Background The Cancer Genome Atlas (TCGA) project is a large-scale effort with
the goal of identifying novel molecular aberrations in glioblastoma (GBM). Methods Here, we …
the goal of identifying novel molecular aberrations in glioblastoma (GBM). Methods Here, we …