Evidence map›Paper›PMID 41292772›Full record

ArticlebioRxiv : the preprint server for biology2025

Elucidating Neurodevelopmental Trajectories in Cancer with Topic Modeling: Revealing Persistent External Granule Layer Lineages in Medulloblastoma.

Ashmitha Rajendran, Parthiv Haldipur, Sonali Arora, Kaustubh Grama, Saanvi S Subramanian, Leyre Merino Galan, David Johnson, Kimberly A Aldinger, Jay Shendure, Kathleen J Millen and 2 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Ashmitha RajendranDepartment of Biomedical Informatics and Medical Education, University of Washington School of Medicine, Seattle, WA.ORCID 0000-0003-1300-0774
Parthiv HaldipurNorcliffe Foundation Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA, USA.
Sonali AroraHuman Biology Division, Fred Hutchinson Cancer Center, Seattle, WA.
Kaustubh GramaWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA.
Saanvi S SubramanianDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA.
Leyre Merino GalanBen Towne Center for Childhood Cancer and Blood Disorders Research, Seattle Children's Research Institute, Seattle, WA.
David JohnsonBen Towne Center for Childhood Cancer and Blood Disorders Research, Seattle Children's Research Institute, Seattle, WA.
Kimberly A AldingerNorcliffe Foundation Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA, USA.ORCID 0000-0002-5406-8911
Jay ShendureDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Kathleen J MillenNorcliffe Foundation Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA, USA.
John H GennariDepartment of Biomedical Informatics and Medical Education, University of Washington School of Medicine, Seattle, WA.
Siobhan S PattwellBen Towne Center for Childhood Cancer and Blood Disorders Research, Seattle Children's Research Institute, Seattle, WA.

Funding

University of Washington Biomedical Informatics and Data Science Research Training ProgramT15LM007442 · NLM · UNIVERSITY OF WASHINGTON · PI JOHN H. GENNARI, Andrea L. Hartzler · 2002 to 2026
$19.6M
Pathological Mechanisms of Human Cerebellar MalformationsR37NS095733 · NINDS · SEATTLE CHILDREN'S HOSPITAL · PI Kathleen Joyce Millen · 2021 to 2026
$5.5M
Mapping the Cerebellar Origins of Medulloblastoma SubgroupsR01CA270785 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Paul Northcott · 2023 to 2026
$2.8M
Characterizing an alternatively spliced NTRK2 isoform in development and cancerK22CA258953 · NCI · SEATTLE CHILDREN'S HOSPITAL · PI PATTWELL, SIOBHAN · 2021 to 2023
$637k
Defining human-specific rhombic lip developmental mechanismsR21NS133390 · NINDS · SEATTLE CHILDREN'S HOSPITAL · PI HALDIPUR, PARTHIV · 2023 to 2023
$541k
Investigating Cerebellar Development in Ferrets: Implications for Modelling Human Cerebellar Development and DiseaseR21NS142543 · NINDS · SEATTLE CHILDREN'S HOSPITAL · PI HALDIPUR, PARTHIV · 2025 to 2025
$516k
In vitro approaches to study human cerebellar developmentR21NS138661 · NINDS · SEATTLE CHILDREN'S HOSPITAL · PI HALDIPUR, PARTHIV · 2024 to 2024
$479k
NCI NIH HHS K22 CA258953NCI NIH HHS R01 CA270785NINDS NIH HHS R21 NS133390NINDS NIH HHS R21 NS138661NINDS NIH HHS R21 NS142543NINDS NIH HHS R37 NS095733NLM NIH HHS T15 LM007442
6 · The paper itself

Abstract

The cerebellar rhombic lip generates cerebellar progenitors and neurons that ultimately differentiate to comprise over half of all neurons in the adult human brain. Standard clustering approaches often fragment or miss rhombic lip progenitor populations entirely due to their transient nature, small size, and rapid state transitions, leaving fundamental questions unanswered about normal cerebellar development and how such processes may be hijacked in pediatric brain cancer. Medulloblastoma, the most common malignant pediatric brain tumor, affects approximately 500 children annually in the United States with overall survival rates varying dramatically by subgroup. Sonic hedgehog (SHH) medulloblastoma, comprising 25-30% of cases, arises from rhombic lip-derived granule neuron precursors (GNP) within the external granule layer (EGL) and has particularly poor outcomes in several subtypes (5-year survival ~41%). Using our topic modeling framework on over one million fetal cerebellar nuclei, we identify proliferative rhombic lip and EGL states that bifurcate into distinct glial and neuronal lineages through intermediate progenitors and capture a portion of the developmental spectrum form outer EGL (oEGL) proliferation through inner EGL (iEGL) differentiation. These developmental signatures (topics) persist in medulloblastoma, validating GNP origins of SHH tumors and revealing age-specific molecular programs that correspond to distinct stages of EGL development within SHH subtypes. Our transferable framework enables systematic comparison of developmental and disease states across technologies without data integration, solving a fundamental challenge as genomic atlases expand.

Indexed as

cell type annotationcerebellar developmentmedulloblastomanatural language processingpediatric brain cancerSHH subgroupsingle-cell RNA sequencingTopic modeling

Identifiers

PMID41292772
PMCPMC12642311

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.