Evidence map›Paper›PMID 40466635›Full record

ArticleCell genomics2025

Pisces: A multi-modal data augmentation approach for drug combination synergy prediction.

Hanwen Xu, Jiacheng Lin, Addie Woicik, Zixuan Liu, Jianzhu Ma, Sheng Zhang, Hoifung Poon, Liewei Wang, Sheng Wang

Abstract read
In one paragraph

Article in Cell genomics, 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

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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

9 authors.

Hanwen XuSchool of Computer Science and Engineering, University of Washington, Seattle, WA, USA.
Jiacheng LinDepartment of Computer Science, University of Illinois Urbana-Champaign, Champaign, IL, USA.
Addie WoicikSchool of Computer Science and Engineering, University of Washington, Seattle, WA, USA.
Zixuan LiuSchool of Computer Science and Engineering, University of Washington, Seattle, WA, USA.
Jianzhu MaDepartment of Electronic Engineering, Tsinghua University, Beijing, China.
Sheng ZhangMicrosoft Research, Redmond, WA, USA.
Hoifung PoonMicrosoft Research, Redmond, WA, USA.
Liewei WangMayo Clinic, Rochester, MN, USA.
Sheng WangSchool of Computer Science and Engineering, University of Washington, Seattle, WA, USA. Electronic address: swang@cs.washington.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug combination therapy is promising for cancer treatment by reducing resistance and improving efficacy. Machine learning approaches to predicting drug combinations require massive training data. Here, we propose Pisces, a novel machine learning approach for drug combination synergy prediction. The key idea is to augment the sparse dataset by creating multiple views for each drug combination based on different modalities. We combined eight modalities of a drug to create 64 augmented views. By treating each augmented view as a separate instance, Pisces can process any number of drug modalities, circumventing the issue of missing modality. Pisces obtained state-of-the-art results on cell-line-based and xenograft-based drug synergy predictions and drug-drug interaction prediction. By interpreting Pisces's predictions using a genetic interaction network, we identified a breast cancer drug-sensitive pathway from BRCA cell lines. Collectively, the results show that Pisces effectively predicts drug synergy and drug-drug interactions through data augmentation and can be applied to various biological applications.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsMachine LearningAnimalsCell Line, TumorDrug InteractionsDrug SynergismDrug Therapy, CombinationFemaleHumanscancer treatmentdata augmentationdrug combination therapymulti-modal learning

Identifiers

PMID40466635
PMCPMC12278649

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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.