Evidence map›Paper›PMID 40637234›Full record

ArticleNucleic acids research2025

Comprehensive analysis of mutational processes across 20 000 adult and pediatric tumors.

Matteo Villa, Federica Malighetti, Luca De Sano, Alberto Maria Villa, Nicoletta Cordani, Andrea Aroldi, Marco Antoniotti, Giulio Caravagna, Alex Graudenzi, Rocco Piazza and 2 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Matteo VillaDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza 20900, Italy.
Federica MalighettiDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza 20900, Italy.
Luca De SanoDepartment of Informatics, Systems and Communication, University of Milano-Bicocca, Milan 20126, Italy.
Alberto Maria VillaDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza 20900, Italy.
Nicoletta CordaniDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza 20900, Italy.
Andrea AroldiDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza 20900, Italy.
Marco AntoniottiDepartment of Informatics, Systems and Communication, University of Milano-Bicocca, Milan 20126, Italy.ORCID 0000-0002-2823-6838
Giulio CaravagnaDepartment of Mathematics and Geosciences, University of Trieste, Trieste 34128, Italy.ORCID 0000-0003-4240-3265
Alex GraudenziDepartment of Informatics, Systems and Communication, University of Milano-Bicocca, Milan 20126, Italy.ORCID 0000-0001-5452-1918
Rocco PiazzaDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza 20900, Italy.
Luca MologniDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza 20900, Italy.
Daniele RamazzottiDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza 20900, Italy.ORCID 0000-0002-6087-2666

Funding

AIRC ID 24828Associazione Italiana per la Ricerca sul CancroBicocca 2020 StartingCancer Research UKDepartment of Excellence project PREMIADipartimenti di EccellenzaEuropean Union-NextGenerationEUItalian Foundation for Cancer ResearchItalian Ministry of University and ResearchItalian Ministry of University and Research under PNRR M4C2-I1.3Italian Ministry of University and Research under PNRR PE_00000019MIURMURSingle-cell Cancer Evolution LC-01815952/101052609Single-cell Cancer Evolution PPPA-2021-AIPCSingle-cell Cancer Evolution PPPA2027UNIque approach for artificial intelligence data-driven solutions to fight Childhood cAncer FOR EuropeUniversità degli Studi di Milano-BicoccaUniversity of Milano-Bicocca
6 · The paper itself

Abstract

Despite being a consolidated practice in modern cancer genomics, mutational signature analysis poses various challenges. First, determining the number of signatures is a complex task and depends on heuristics. Second, several signatures lack a clear etiology, raising concerns about whether they result from computational artifacts or actual mutagenic processes. Last, approaches for signature assignment are highly influenced by the catalogue of signatures used for the analysis. To overcome these limitations, we introduce RESOLVE (Robust EStimation Of mutationaL signatures Via rEgularization), a framework designed for the efficient extraction, assignment, and confidence estimation of mutational signatures. RESOLVE enables the stratification of cancer genomes according to the active mutational processes, providing insights into those that are consistently shared among various cancer types. We applied RESOLVE to 20 000 samples from adult and pediatric cancers, providing a comprehensive characterization of subtypes associated with specific mutational processes and alterations in driver genes. Our analysis demonstrates that RESOLVE accurately fits observed mutations with a smaller set of signatures compared to existing catalogues, suggesting the existence of a limited number of dominant mutational processes in cancer genomes. Clustering analysis revealed distinct patient groups characterized by specific signatures, with significant associations between certain signatures and patient prognosis. Additionally, we identified strong associations between signatures and driver gene mutations, offering insights into cancer subtype mechanisms and evolution. Our findings highlight the efficiency of RESOLVE and its potential impact on personalized cancer treatment.

Indexed as

MutationNeoplasmsAdultChildCluster AnalysisDNA Mutational AnalysisGenomicsHumansPrognosis

Identifiers

PMID40637234
PMCPMC12242766

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Registered trials

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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.