Evidence map›Paper›PMID 42016166›Full record

ArticleiScience2026

The MOGA multi-modal framework based on graph augmentation networks for drug response prediction.

Kaiyuan Zhang, Runze Wang, Tianyi Zang, Yanli Zhao

Abstract read
In one paragraph

Article in iScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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.

Kaiyuan ZhangFaculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang 150001, China.
Runze WangFaculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang 150001, China.
Tianyi ZangFaculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang 150001, China.
Yanli ZhaoMedical College, Qinghai University, Xining, Qinghai 810016, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Personalized cancer treatment faces challenges due to tumor heterogeneity and limitations in existing computational methods regarding multi-omics integration. To address these limitations, this study presents MOGA, an advanced framework for drug response prediction. MOGA constructs a heterogeneous graph integrating cell line multi-omics, drug chemical structures, and response data, utilizing a relational graph convolutional network (RGCN) to model complex interactions. Crucially, a type-specific graph augmentation strategy is proposed, which categorizes neighbor influence to preserve critical sensitive signals while reducing noise from non-sensitive nodes. Experimental results demonstrate that MOGA significantly outperforms competitive baselines in both AUROC and AUPR. Ablation studies and case analysis confirm that the integration of multi-omics data and the targeted augmentation mechanism are central to these performance gains, validating MOGA's potential for precision oncology.

Indexed as

Artificial intelligenceBioinformaticsDrug dispensingOmicsPrecision medicine

Identifiers

PMID42016166
PMCPMC13092757

What OpenQuestion holds

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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.