Evidence map›Paper›PMID 41057477›Full record

ArticleCommunications biology2025

OncoMark: a high-throughput neural multi-task learning framework for comprehensive cancer hallmark quantification.

Shreyansh Priyadarshi, Camellia Mazumder, Bhavesh Neekhra, Sayan Biswas, Debojyoti Chowdhury, Debayan Gupta, Shubhasis Haldar

Abstract read
In one paragraph

Article in Communications biology, 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. Article
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

7 authors.

Shreyansh PriyadarshiDepartment of Computer Science, Ashoka University, Sonipat, Haryana, 131029, India.ORCID http://orcid.org/0000-0002-6230-4574
Camellia MazumderDepartment of Chemical and Biological Sciences, S.N. Bose National Centre for Basic Sciences, Kolkata, 700106, India.
Bhavesh NeekhraDepartment of Computer Science, Ashoka University, Sonipat, Haryana, 131029, India.ORCID http://orcid.org/0000-0001-5468-0812
Sayan BiswasDepartment of Chemical and Biological Sciences, S.N. Bose National Centre for Basic Sciences, Kolkata, 700106, India.
Debojyoti ChowdhuryDepartment of Chemical and Biological Sciences, S.N. Bose National Centre for Basic Sciences, Kolkata, 700106, India.
Debayan GuptaDepartment of Computer Science, Ashoka University, Sonipat, Haryana, 131029, India. debayan.gupta@ashoka.edu.in.ORCID http://orcid.org/0000-0002-4457-1556
Shubhasis HaldarDepartment of Chemical and Biological Sciences, S.N. Bose National Centre for Basic Sciences, Kolkata, 700106, India. shubhasis.haldar@bose.res.in.ORCID http://orcid.org/0000-0002-4304-5570

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantifying the biological processes that drive cancer progression remains a key challenge in oncology. Although the hallmarks of cancer provide a foundational framework for understanding tumor behavior, existing diagnostic tools rarely measure these hallmarks directly. Here we present a neural multi-task learning-based framework that estimates hallmark activity using gene expression data from tumor biopsies. The model was trained on transcriptomic profiles from 941 tumors spanning 14 tissue types and tested on five independent datasets. It predicts the activity of ten cancer hallmarks simultaneously and with high accuracy. Additional validation on large-scale datasets including normal and cancer samples confirmed its sensitivity and specificity. Predicted hallmark activity was associated with clinical staging, suggesting biological relevance. A web-based tool was developed to facilitate integration into research and clinical workflows. This approach enables efficient analysis of transcriptomic data to inform understanding of tumor biology and support individualized treatment strategies.

Indexed as

NeoplasmsGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMachine LearningTranscriptome

Identifiers

PMID41057477
PMCPMC12504664

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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.