Evidence map›Paper›PMID 38561679›Full record

ArticleBMC bioinformatics2024

MFSynDCP: multi-source feature collaborative interactive learning for drug combination synergy prediction.

Yunyun Dong, Yunqing Chang, Yuxiang Wang, Qixuan Han, Xiaoyuan Wen, Ziting Yang, Yan Zhang, Yan Qiang, Kun Wu, Xiaole Fan and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
8.3field-weighted citation impact, top 2% of its field
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

13 citing papers in PubMed, 23 citations in OpenAlex.

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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

11 authors at 5 institutions in 2 countries.

Yunyun DongSchool of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China. dongyunyun@tyut.edu.cn.
Yunqing ChangSchool of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China.
Yuxiang WangSchool of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China.
Qixuan HanSchool of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China.
Xiaoyuan WenSchool of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China.
Ziting YangSchool of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China.
Yan ZhangSchool of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China.
Yan QiangCollege of Computer Science and Technology (College of Data Science), Taiyuan University of Technology, Taiyuan, Shanxi, China. qiangyan@tyut.edu.cn.
Kun WuSchool of Computing, University of Leeds, Leeds, West Yorkshire, UK.
Xiaole FanInformation Management Department, Shanxi Provincial People's Hospital, Taiyuan, Shanxi, China.
Xiaoqiang RenInformation Management Department, Shanxi Provincial People's Hospital, Taiyuan, Shanxi, China.
Taiyuan University of Technology · CNTaiyuan University of Science and Technology · CNShaanxi Provincial People's Hospital · CNShanxi Medical University · CNUniversity of Leeds · GB

Funding

Applied Basic Research Program of Shanxi Province 202203021212207Key Research and Development Program of Shanxi Province 202102020101007National Natural Science Foundation of China 62306206
6 · The paper itself

Abstract

Drug combination therapy is generally more effective than monotherapy in the field of cancer treatment. However, screening for effective synergistic combinations from a wide range of drug combinations is particularly important given the increase in the number of available drug classes and potential drug-drug interactions. Existing methods for predicting the synergistic effects of drug combinations primarily focus on extracting structural features of drug molecules and cell lines, but neglect the interaction mechanisms between cell lines and drug combinations. Consequently, there is a deficiency in comprehensive understanding of the synergistic effects of drug combinations. To address this issue, we propose a drug combination synergy prediction model based on multi-source feature interaction learning, named MFSynDCP, aiming to predict the synergistic effects of anti-tumor drug combinations. This model includes a graph aggregation module with an adaptive attention mechanism for learning drug interactions and a multi-source feature interaction learning controller for managing information transfer between different data sources, accommodating both drug and cell line features. Comparative studies with benchmark datasets demonstrate MFSynDCP's superiority over existing methods. Additionally, its adaptive attention mechanism graph aggregation module identifies drug chemical substructures crucial to the synergy mechanism. Overall, MFSynDCP is a robust tool for predicting synergistic drug combinations. The source code is available from GitHub at https://github.com/kkioplkg/MFSynDCP .

Indexed as

BenchmarkingSimulation TrainingCell LineDrug CombinationsDrug Therapy, CombinationDrug CombinationsAnti-tumorDeep learningDrug combinationGraph attention networkSynergistic effect

Identifiers

PMID38561679
PMCPMC10985899
OpenAlexW4393374578

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.