Evidence map›Paper›PMID 38256095›Full record

ArticleInternational journal of molecular sciences2024

Comparative Transcriptomic Analysis of Cerebellar Astrocytes across Developmental Stages and Brain Regions.

Wookbong Kwon, Dong-Joo Choi, Kwanha Yu, Michael R Williamson, Sanjana Murali, Yeunjung Ko, Junsung Woo, Benjamin Deneen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Medulloblastoma: biology and immunotherapy.Frontiers in immunology · 2025
    Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Wookbong KwonCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77030, USA.
Dong-Joo ChoiCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77030, USA.
Kwanha YuCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77030, USA.
Michael R WilliamsonCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77030, USA.
Sanjana MuraliCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77030, USA.
Yeunjung KoCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77030, USA.
Junsung WooCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77030, USA.
Benjamin DeneenCenter for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX 77030, USA.
Baylor College of Medicine · US

Funding

Preclinical and Clincial OutcomesP50HD103555 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI Sandesh Chakravarthy Sreenath Nagamani, David Loren Nelson · 2020 to 2026
$9.9M
Astrocyte Transcriptional Dependencies in Brain CircuitsR35NS132230 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI Benjamin Deneen · 2023 to 2026
$3.5M
Transcriptional Regulation in ZFTA-RELA EpendymomaR01CA284455 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Benjamin Deneen, Stephen C Mack · 2023 to 2026
$2.5M
Defining Roles for Astrocyte Subpopulations in the Aging BrainR01AG071687 · NIA · BAYLOR COLLEGE OF MEDICINE · PI DENEEN, BENJAMIN · 2021 to 2025
$2.0M
Functional Genomics of High Grade GliomaR50CA252125 · NCI · BAYLOR COLLEGE OF MEDICINE · PI YU, KWANHA · 2020 to 2024
$761k
Investigating the role of astrocyte specific NFIA during initiation and progression of AD pathogenesisK01AG083128 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Dongjoo Choi · 2023 to 2026
$409k
NCI NIH HHS R01 CA284455NCI NIH HHS R50 CA252125NIA NIH HHS K01 AG083128NIA NIH HHS R01 AG071687NICHD NIH HHS P50 HD103555NINDS NIH HHS R35 NS132230
6 · The paper itself

Abstract

Astrocytes are the most abundant glial cell type in the central nervous system, and they play a crucial role in normal brain function. While gliogenesis and glial differentiation occur during perinatal cerebellar development, the processes that occur during early postnatal development remain obscure. In this study, we conducted transcriptomic profiling of postnatal cerebellar astrocytes at postnatal days 1, 7, 14, and 28 (P1, P7, P14, and P28), identifying temporal-specific gene signatures at each specific time point. Comparing these profiles with region-specific astrocyte differentially expressed genes (DEGs) published for the cortex, hippocampus, and olfactory bulb revealed cerebellar-specific gene signature across these developmental timepoints. Moreover, we conducted a comparative analysis of cerebellar astrocyte gene signatures with gene lists from pediatric brain tumors of cerebellar origin, including ependymoma and medulloblastoma. Notably, genes downregulated at P14, such as Kif11 and HMGB2, exhibited significant enrichment across all pediatric brain tumor groups, suggesting the importance of astrocytic gene repression during cerebellar development to these tumor subtypes. Collectively, our studies describe gene expression patterns during cerebellar astrocyte development, with potential implications for pediatric tumors originating in the cerebellum.

Indexed as

Brain NeoplasmsCerebellar NeoplasmsAstrocytesBrainCerebellumChildFemaleGene Expression ProfilingHumansPregnancyTranscriptomeastrocytecerebellumpediatric brain tumorspostnatal developmenttranscriptome

Identifiers

PMID38256095
PMCPMC10816327
OpenAlexW4390881881

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.