Evidence map›Paper›PMID 33262326›Full record

ArticleNature communications2020

Leveraging multi-way interactions for systematic prediction of pre-clinical drug combination effects.

Heli Julkunen, Anna Cichonska, Prson Gautam, Sandor Szedmak, Jane Douat, Tapio Pahikkala, Tero Aittokallio, Juho Rousu

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
17.0field-weighted citation impact, top 1% 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

70 citing papers in PubMed, 1 synthesis or guideline pooled it, 147 citations in OpenAlex.

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  17. Scaling up drug combination surface prediction.Briefings in bioinformatics · 2025
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10 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 2 countries.

Heli JulkunenDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Espoo, Finland.ORCID 0000-0002-4282-0248
Anna CichonskaDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Espoo, Finland.ORCID 0000-0003-1072-8858
Prson GautamInstitute for Molecular Medicine Finland FIMM, University of Helsinki, Helsinki, Finland.ORCID 0000-0002-1154-8501
Sandor SzedmakDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Espoo, Finland.ORCID 0000-0003-1469-2215
Jane DouatDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Espoo, Finland.
Tapio PahikkalaDepartment of Future Technologies, University of Turku, Turku, Finland.ORCID 0000-0003-4183-2455
Tero AittokallioDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Espoo, Finland. tero.aittokallio@helsinki.fi.ORCID 0000-0002-0886-9769
Juho RousuDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Espoo, Finland. juho.rousu@aalto.fi.ORCID 0000-0002-0705-4314
Helsinki Institute for Information Technology · FIUniversity of Helsinki · FIOslo University Hospital · NOUniversity of Turku · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present comboFM, a machine learning framework for predicting the responses of drug combinations in pre-clinical studies, such as those based on cell lines or patient-derived cells. comboFM models the cell context-specific drug interactions through higher-order tensors, and efficiently learns latent factors of the tensor using powerful factorization machines. The approach enables comboFM to leverage information from previous experiments performed on similar drugs and cells when predicting responses of new combinations in so far untested cells; thereby, it achieves highly accurate predictions despite sparsely populated data tensors. We demonstrate high predictive performance of comboFM in various prediction scenarios using data from cancer cell line pharmacogenomic screens. Subsequent experimental validation of a set of previously untested drug combinations further supports the practical and robust applicability of comboFM. For instance, we confirm a novel synergy between anaplastic lymphoma kinase (ALK) inhibitor crizotinib and proteasome inhibitor bortezomib in lymphoma cells. Overall, our results demonstrate that comboFM provides an effective means for systematic pre-screening of drug combinations to support precision oncology applications.

Indexed as

Machine LearningAntineoplastic AgentsBortezomibCell Line, TumorCrizotinibDrug InteractionsHumansLymphomaPrecision MedicineAntineoplastic AgentsBortezomibCrizotinib

Identifiers

PMID33262326
PMCPMC7708835
OpenAlexW3107514561

What OpenQuestion holds

Textmetadata
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.