Evidence map›Paper›PMID 41465461›Full record

ArticleInternational journal of molecular sciences2025

Subtype-Specific mRNA Signatures of Human Ribosomal Proteins in Pediatric Cancers.

Anshuman Panda, Anupama Yadav, Gyan Bhanot, Shridar Ganesan

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

4 authors.

Anshuman PandaPerlmutter Cancer Center, New York, NY 10016, USA.ORCID 0000-0001-7917-0317
Anupama YadavDana-Farber Cancer Institute, Boston, MA 02215, USA.
Gyan BhanotRutgers Cancer Institute of New Jersey, New Brunswick, NJ 08903, USA.
Shridar GanesanPerlmutter Cancer Center, New York, NY 10016, USA.

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Tracie Saunders · 1997 to 2026
$94.5M
Impact of mutation burden on cancer growth and the immune landscapeR01CA243547 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI WHITE, EILEEN P. · 2020 to 2024
$3.2M
Computerized histologic image predictor of cancer outcomeR01CA202752 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI FELDMAN, MICHAEL D, GANESAN, SHRIDAR · 2016 to 2020
$3.1M
Breast Cancer Research Foundation NAGertrude Fogarty Trust NAHugs for Brady Foundation NANCI NIH HHS P30 CA072720NCI NIH HHS R01 CA202752NCI NIH HHS R01 CA243547United States Department of Defense W81XWH1910821Val Skinner Foundation NA
6 · The paper itself

Abstract

A growing body of recent work suggests the possibility of heterogeneous ribosomal composition. We recently observed subtype-specific mRNA and copy number variation signatures of human ribosomal proteins (RPs) in cancers from human adults, but whether such subtype-specific RP mRNA signatures are also present in human pediatric cancers is currently unknown. In this study, we analyzed mRNA expression data from multiple large pediatric cancer datasets to test for heterogeneity in RP mRNA signatures. We found that different pediatric cancer types have different RP mRNA signatures, sometimes multiple RP mRNA signatures within the same pediatric cancer type, which can be subgroup/subtype-specific (e.g., in Medulloblastoma) or cell-of-origin-specific (e.g., in Acute Lymphoblastic Leukemia (ALL)). In B-cell ALL, we found two RP mRNA subtypes with significantly different prognoses. Consistent with our recent findings in adult cancers, the RP mRNA signature in pediatric cancer is heterogeneous and subtype-specific and may have clinical relevance.

Indexed as

NeoplasmsRibosomal ProteinsRNA, MessengerChildGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMedulloblastomaRibosomal ProteinsRNA, Messengeracute lymphoblastic leukemiaheterogeneous ribosomal compositionmedulloblastomapediatric cancersribosomal proteins

Identifiers

PMID41465461
PMCPMC12733358

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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.