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ASCL1 regulates neurodevelopmental transcription factors and cell cycle genes in glioblastoma

https://doi.org/10.1101/2020.02.20.958132
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/glia.20350openalex-snapshot
Inducible gene deletion in astroglia and radial glia—A valuable tool for functional and lineage analysis
inferredcites →https://doi.org/10.1002/glia.22369openalex-snapshot
The identification of transcriptional targets of Ascl1 in oligodendrocyte development
inferredcites →https://doi.org/10.1002/glia.23344openalex-snapshot
ASCL 1 regulates proliferation of NG 2‐glia in the embryonic and adult spinal cord
inferredcites →https://doi.org/10.1002/pros.22679openalex-snapshot
Human ASH-1 Promotes Neuroendocrine Differentiation in Androgen Deprivation Conditions and Interferes With Androgen Responsiveness in Prostate Cancer Cells
inferredcites →https://doi.org/10.1016/j.ccell.2015.09.007openalex-snapshot
Adult Lineage-Restricted CNS Progenitors Specify Distinct Glioblastoma Subtypes
inferredcites →https://doi.org/10.1016/j.ccell.2016.03.027openalex-snapshot
Olig2-Dependent Reciprocal Shift in PDGF and EGF Receptor Signaling Regulates Tumor Phenotype and Mitotic Growth in Malignant Glioma
inferredcites →https://doi.org/10.1016/j.ccr.2005.07.004openalex-snapshot
Early inactivation of p53 tumor suppressor gene cooperating with NF1 loss induces malignant astrocytoma
inferredcites →https://doi.org/10.1016/j.ccr.2008.12.006openalex-snapshot
Malignant Astrocytomas Originate from Neural Stem/Progenitor Cells in a Somatic Tumor Suppressor Mouse Model
inferredcites →https://doi.org/10.1016/j.ccr.2009.12.020openalex-snapshot
Integrated Genomic Analysis Identifies Clinically Relevant Subtypes of Glioblastoma Characterized by Abnormalities in PDGFRA, IDH1, EGFR, and NF1
inferredcites →https://doi.org/10.1016/j.ccr.2011.01.035openalex-snapshot
The Central Nervous System-Restricted Transcription Factor Olig2 Opposes p53 Responses to Genotoxic Damage in Neural Progenitors and Malignant Glioma
inferredcites →https://doi.org/10.1016/j.cell.2013.09.034openalex-snapshot
The Somatic Genomic Landscape of Glioblastoma
inferredcites →https://doi.org/10.1016/j.cell.2014.02.030openalex-snapshot
Reconstructing and Reprogramming the Tumor-Propagating Potential of Glioblastoma Stem-like Cells
inferredcites →https://doi.org/10.1016/j.celrep.2013.04.021openalex-snapshot
An Aberrant Transcription Factor Network Essential for Wnt Signaling and Stem Cell Maintenance in Glioblastoma
inferredcites →https://doi.org/10.1016/j.celrep.2015.02.025openalex-snapshot
Ascl1 Coordinately Regulates Gene Expression and the Chromatin Landscape during Neurogenesis
inferredcites →https://doi.org/10.1016/j.celrep.2016.06.081openalex-snapshot
ASCL1 and NEUROD1 Reveal Heterogeneity in Pulmonary Neuroendocrine Tumors and Regulate Distinct Genetic Programs
inferredcites →https://doi.org/10.1016/j.celrep.2016.12.064openalex-snapshot
Oncogenes Activate an Autonomous Transcriptional Regulatory Circuit That Drives Glioblastoma
inferredcites →https://doi.org/10.1016/j.cmet.2012.05.001openalex-snapshot
Analysis of Tumor Metabolism Reveals Mitochondrial Glucose Oxidation in Genetically Diverse Human Glioblastomas in the Mouse Brain In Vivo
inferredcites →https://doi.org/10.1016/j.molcel.2010.05.004openalex-snapshot
Simple Combinations of Lineage-Determining Transcription Factors Prime cis-Regulatory Elements Required for Macrophage and B Cell Identities
inferredcites →https://doi.org/10.1016/j.neuron.2007.01.009openalex-snapshot
Olig2-Regulated Lineage-Restricted Pathway Controls Replication Competence in Neural Stem Cells and Malignant Glioma
inferredcites →https://doi.org/10.1016/j.neuron.2011.02.018openalex-snapshot
Proneural Transcription Factors Regulate Different Steps of Cortical Neuron Migration through Rnd-Mediated Inhibition of RhoA Signaling
inferredcites →https://doi.org/10.1016/j.neuron.2014.08.004openalex-snapshot
A Transcriptional Mechanism Integrating Inputs from Extracellular Signals to Activate Hippocampal Stem Cells
inferredcites →https://doi.org/10.1016/j.stem.2011.04.013openalex-snapshot
Deadly Teamwork: Neural Cancer Stem Cells and the Tumor Microenvironment
inferredcites →https://doi.org/10.1016/j.stem.2017.06.004openalex-snapshot
ASCL1 Reorganizes Chromatin to Direct Neuronal Fate and Suppress Tumorigenicity of Glioblastoma Stem Cells
inferredcites →https://doi.org/10.1016/j.yexcr.2005.03.015openalex-snapshot
Roles of bHLH genes in neural stem cell differentiation
inferredcites →https://doi.org/10.1016/s0092-8674(02)00678-5openalex-snapshot
Common Developmental Requirement for Olig Function Indicates a Motor Neuron/Oligodendrocyte Connection
inferredcites →https://doi.org/10.1016/s0896-6273(01)00414-7openalex-snapshot
The bHLH Transcription Factor Olig2 Promotes Oligodendrocyte Differentiation in Collaboration with Nkx2.2
inferredcites →https://doi.org/10.1038/nature05236openalex-snapshot
Glioma stem cells promote radioresistance by preferential activation of the DNA damage response
inferredcites →https://doi.org/10.1038/nature07385openalex-snapshot
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
inferredcites →https://doi.org/10.1038/nature11287openalex-snapshot
A restricted cell population propagates glioblastoma growth after chemotherapy
inferredcites →https://doi.org/10.1038/nature23666openalex-snapshot
Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy
inferredcites →https://doi.org/10.1038/nbt.1630openalex-snapshot
GREAT improves functional interpretation of cis-regulatory regions
inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot
Fast gapped-read alignment with Bowtie 2
inferredcites →https://doi.org/10.1038/nn.2467openalex-snapshot
A robust and high-throughput Cre reporting and characterization system for the whole mouse brain
inferredcites →https://doi.org/10.1038/nn.3790openalex-snapshot
Mutual antagonism between Sox10 and NFIA regulates diversification of glial lineages and glioma subtypes
inferredcites →https://doi.org/10.1038/nn.4638openalex-snapshot
Glia-specific enhancers and chromatin structure regulate NFIA expression and glioma tumorigenesis
inferredcites →https://doi.org/10.1038/nprot.2016.117openalex-snapshot
Analyzing and interpreting genome data at the network level with ConsensusPathDB
inferredcites →https://doi.org/10.1038/s41583-018-0014-3openalex-snapshot
A glial blueprint for gliomagenesis
inferredcites →https://doi.org/10.1038/sj.emboj.7600447openalex-snapshot
Mash1 specifies neurons and oligodendrocytes in the postnatal brain
inferredcites →https://doi.org/10.1038/sj.onc.1208865openalex-snapshot
Upregulation of ASCL1 and inhibition of Notch signaling pathway characterize progressive astrocytoma
inferredcites →https://doi.org/10.1073/pnas.0506580102openalex-snapshot
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
inferredcites →https://doi.org/10.1073/pnas.1219747110openalex-snapshot
Intratumor heterogeneity in human glioblastoma reflects cancer evolutionary dynamics
inferredcites →https://doi.org/10.1089/thy.2005.15.511openalex-snapshot
Medullary Thyroid Cancer: The Functions of raf-1 and Human Achaete-scute Homologue-1
inferredcites →https://doi.org/10.1093/bioinformatics/btp616openalex-snapshot
edgeR : a Bioconductor package for differential expression analysis of digital gene expression data
inferredcites →https://doi.org/10.1093/bioinformatics/btr509openalex-snapshot
A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data
inferredcites →https://doi.org/10.1093/neuonc/now207openalex-snapshot
CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2009–2013
inferredcites →https://doi.org/10.1093/neuonc/now233openalex-snapshot
A novel NFIA-NFκB feed-forward loop contributes to glioblastoma cell survival
inferredcites →https://doi.org/10.1101/gad.627811openalex-snapshot
A novel function of the proneural factor Ascl1 in progenitor proliferation identified by genome-wide characterization of its targets
inferredcites →https://doi.org/10.1101/gad.862101openalex-snapshot
Ablation of NF1 function in neurons induces abnormal development of cerebral cortex and reactive gliosis in the brain
inferredcites →https://doi.org/10.1101/gr.224360.117openalex-snapshot
Intrinsic DNA binding properties demonstrated for lineage-specifying basic helix-loop-helix transcription factors
inferredcites →https://doi.org/10.1126/science.1254257openalex-snapshot
Single-cell RNA-seq highlights intratumoral heterogeneity in primary glioblastoma
inferredcites →https://doi.org/10.1158/0008-5472.can-03-3524openalex-snapshot
Somatic Mutation of p53 Leads to Estrogen Receptor α-Positive and -Negative Mouse Mammary Tumors with High Frequency of Metastasis
inferredcites →https://doi.org/10.1158/1078-0432.ccr-09-2850openalex-snapshot
The Telomerase Antagonist, Imetelstat, Efficiently Targets Glioblastoma Tumor-Initiating Cells Leading to Decreased Proliferation and Tumor Growth
inferredcites →https://doi.org/10.1186/1471-213x-1-4openalex-snapshot
Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus
inferredcites →https://doi.org/10.1186/1755-8794-1-17openalex-snapshot
Pro-neural transcription factors as cancer markers
inferredcites →https://doi.org/10.1186/gb-2013-14-4-r36openalex-snapshot
TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1200/jco.2017.73.9540openalex-snapshot
Brain Tumor Stem Cells Remain in Play
inferredcites →https://doi.org/10.1242/dev.001255openalex-snapshot
Combinatorial actions of patterning and HLH transcription factors in the spatiotemporal control of neurogenesis and gliogenesis in the developing spinal cord
inferredcites →https://doi.org/10.1242/dev.015370openalex-snapshot
Ascl1 is required for oligodendrocyte development in the spinal cord
inferredcites →https://doi.org/10.1242/dev.01859openalex-snapshot
Sequential roles for Mash1 and Ngn2 in the generation of dorsal spinal cord interneurons
inferredcites →https://doi.org/10.1242/dev.034546openalex-snapshot
Insm1 (IA-1) is an essential component of the regulatory network that specifies monoaminergic neuronal phenotypes in the vertebrate hindbrain
inferredcites →https://doi.org/10.1242/dev.105270openalex-snapshot
Ascl1 controls the number and distribution of astrocytes and oligodendrocytes in the gray matter and white matter of the spinal cord
inferredcites →https://doi.org/10.1242/dev.105866openalex-snapshot
A transcription factor network specifying inhibitory versus excitatory neurons in the dorsal spinal cord
inferredcites →https://doi.org/10.1371/journal.pone.0007752openalex-snapshot
Glioblastoma Subclasses Can Be Defined by Activity among Signal Transduction Pathways and Associated Genomic Alterations
inferredcites →https://doi.org/10.1371/journal.pone.0018472openalex-snapshot
Ascl1 (Mash1) Defines Cells with Long-Term Neurogenic Potential in Subgranular and Subventricular Zones in Adult Mouse Brain
inferredcites →https://doi.org/10.1371/journal.pone.0020041openalex-snapshot
Glioblastoma Models Reveal the Connection between Adult Glial Progenitors and the Proneural Phenotype
inferredcites →https://doi.org/10.1371/journal.pone.0024807openalex-snapshot
Direct In Vivo Evidence for Tumor Propagation by Glioblastoma Cancer Stem Cells
inferredcites →https://doi.org/10.1523/jneurosci.0126-07.2007openalex-snapshot
The Proneural GeneMash1Specifies an Early Population of Telencephalic Oligodendrocytes
inferredcites →https://doi.org/10.1523/jneurosci.0805-13.2013openalex-snapshot
Ascl1/Mash1 Promotes Brain Oligodendrogenesis during Myelination and Remyelination
inferredcites →https://doi.org/10.1523/jneurosci.1860-14.2014openalex-snapshot
An RNA-Sequencing Transcriptome and Splicing Database of Glia, Neurons, and Vascular Cells of the Cerebral Cortex
inferredcites →https://doi.org/10.1523/jneurosci.3178-07.2007openalex-snapshot
In VivoAnalysis of Ascl1 Defined Progenitors Reveals Distinct Developmental Dynamics during Adult Neurogenesis and Gliogenesis
inferredcites →https://doi.org/10.1634/stemcells.2008-0493openalex-snapshot
SOX2 Silencing in Glioblastoma Tumor-Initiating Cells Causes Stop of Proliferation and Loss of Tumorigenicity
inferredcites →https://doi.org/10.21037/tlcr.2018.02.02openalex-snapshot
Small cell lung cancer tumors and preclinical models display heterogeneity of neuroendocrine phenotypes
inferredcites →https://doi.org/10.3171/2015.4.jns142200openalex-snapshot
Glioblastoma in the elderly: the effect of aggressive and modern therapies on survival

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1101/2020.10.18.344515openalex-snapshot
Unraveling the transcriptional networks that drive oligodendrocyte fate specification in Sonic hedgehog-responsive neocortical progenitors
inferred← citeshttps://doi.org/10.1101/2023.09.30.560206openalex-snapshot
Glioblastoma initiation, migration, and cell types are regulated by core bHLH transcription factors ASCL1 and OLIG2
inferred← citeshttps://doi.org/10.1523/jneurosci.0240-26.2026openalex-snapshot
ASCL1 and OLIG2 Expression Dynamics Control Glial Cell Fate and Regional Diversity in the Dorsal Forebrain
inferred← citeshttps://doi.org/10.3390/cells9102304openalex-snapshot
Oncogenic and Tumor-Suppressive Functions of NOTCH Signaling in Glioma
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