Evidence map›Paper›PMID 42491358›Full record

ArticleComputational and structural biotechnology journal2026

NCES: A Cell-Specific Network-Augmented Essentiality Framework for Cancer Therapeutic Target Discovery.

Jinmyung Jung, Sunyong Yoo

Abstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2026. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Jinmyung JungDivision of Data Science, College of Information and Communication Technology Convergence, The University of Suwon, Hwaseong 18323, Republic of Korea.ORCID https://orcid.org/0000-0002-4962-8347
Sunyong YooDepartment of Intelligent Electronics and Computer Engineering, Chonnam National University, Gwangju 61186, Republic of Korea.ORCID https://orcid.org/0000-0003-0925-1853

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying effective therapeutic targets remains a central challenge in cancer research. CRISPR-Cas9 knockout screens have provided valuable insights into gene essentiality; however, using essentiality at the level of individual genes often fails to reliably distinguish true therapeutic targets from nonfunctional candidates. To address this limitation, we developed the neighbor-correlation essentiality score (NCES), a network-augmented framework that leverages the essentialities of functionally active neighboring genes. NCES combines DepMap CERES scores, which estimate gene essentiality from CRISPR-Cas9 knockout screens, with protein-protein interaction networks. Interaction weights are assigned to network neighbors based on cell-line-specific expression correlations derived from CRISPR knockout or compound-perturbation profiles. The proposed NCES framework was systematically evaluated across 7 cancer cell lines against therapeutic target gold standards. NCES variants consistently outperformed approaches based solely on individual gene essentiality, with the CRISPR-weighted variant achieving the best performance, yielding AUROCs of 0.794 and 0.779 against the Therapeutic Target Database and DrugBank gold standards, respectively. Statistical testing demonstrated that weighted NCES variants significantly improved predictive accuracy over their unweighted counterpart. Finally, several high-ranking genes beyond current gold-standard datasets, including

Identifiers

PMID42491358
PMCPMC13376377

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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.