Evidence map›Paper›PMID 40740860›Full record

ArticleFrontiers in oncology2025

Machine learning-based single-sample molecular classifier for cancer grading.

Zoia Antysheva, Nikita Kotlov, Mariia V Guryleva, Ivan Valiev, Viktor Svekolkin, Anna Belozerova, Sheila T Yong, Dmitry Tabakov, Alexander Bagaev, Vladimir Kushnarev

Abstract read
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Article in Frontiers in oncology, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Zoia Antysheva *Research and Development, BostonGene Corporation, Waltham, MA, United States.
Nikita Kotlov *Research and Development, BostonGene Corporation, Waltham, MA, United States.
Mariia V GurylevaResearch and Development, BostonGene Corporation, Waltham, MA, United States.
Ivan ValievResearch and Development, BostonGene Corporation, Waltham, MA, United States.
Viktor SvekolkinResearch and Development, BostonGene Corporation, Waltham, MA, United States.
Anna BelozerovaResearch and Development, BostonGene Corporation, Waltham, MA, United States.
Sheila T Yong *Research and Development, BostonGene Corporation, Waltham, MA, United States.
Dmitry Tabakov *Research and Development, BostonGene Corporation, Waltham, MA, United States.
Alexander BagaevResearch and Development, BostonGene Corporation, Waltham, MA, United States.
Vladimir KushnarevResearch and Development, BostonGene Corporation, Waltham, MA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor subtyping based on morphological grade is used in cancer treatment and management decision-making and to determine a patient's prognosis. While low- and high-grade tumors are predictive of patient survival for many cancers, tumors of intermediate morphological grades are considered unreliable due to interobserver variability and thus do not have clear prognostic significance. To address this issue, we devised a molecular-based classifier that uses gene expression data from RNA sequencing (RNA-seq) or microarray profiling to predict high- and low-grade risk groups for breast, lung, and renal cancers. For this classifier, we developed a preprocessing procedure that only required expression data from a single sample, without the need for any batch correction or cohort scaling. This classifier, while trained only on RNA sequencing data, achieves highly accurate risk predictions on both RNA-seq and microarray data. First, the molecular grades (mGrades) predicted by this classifier correlated strongly with the pathologist-assigned histological grades and clinical stage. Next, we showed that mGrades were effective in assessing risk levels for G2 samples. Finally, we identified common and unique biological and genetic features in samples of low and high mGrades across breast, lung, and renal cancers. Gene expression patterns as revealed by the classifier can provide useful information for both research and diagnostic purposes.

Indexed as

cancer diagnosticsgene expressionmolecular graderisk assessmenttumor cell differentiationtumor grade

Identifiers

PMID40740860
PMCPMC12307393

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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.