Evidence map›Paper›PMID 30577754›Full record

ArticleBMC bioinformatics2018

Predicting tumor cell line response to drug pairs with deep learning.

Fangfang Xia, Maulik Shukla, Thomas Brettin, Cristina Garcia-Cardona, Judith Cohn, Jonathan E Allen, Sergei Maslov, Susan L Holbeck, James H Doroshow, Yvonne A Evrard and 2 more

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing 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

59 citing papers in PubMed.

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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

12 authors.

Fangfang XiaComputing, Environment and Life Sciences, Argonne National Laboratory, Lemont, IL, USA. fangfang@anl.gov.
Maulik ShuklaComputing, Environment and Life Sciences, Argonne National Laboratory, Lemont, IL, USA.
Thomas BrettinComputing, Environment and Life Sciences, Argonne National Laboratory, Lemont, IL, USA.
Cristina Garcia-CardonaCenter for Nonlinear Studies, Los Alamos National Laboratory, Los Alamos, NM, USA.
Judith CohnComputer Science, Los Alamos National Laboratory, Los Alamos, NM, USA.
Jonathan E AllenComputation Directorate, Lawrence Livermore National Laboratory, Livermore, CA, USA.
Sergei MaslovDepartment of Bioengineering and Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Susan L HolbeckDevelopmental Therapeutics Branch, National Cancer Institute, Frederick, MD, USA.
James H DoroshowDevelopmental Therapeutics Branch, National Cancer Institute, Frederick, MD, USA.
Yvonne A EvrardDevelopmental Therapeutics Branch, National Cancer Institute, Frederick, MD, USA.
Eric A StahlbergData Science and Information Technology Program, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
Rick L StevensComputing, Environment and Life Sciences, Argonne National Laboratory, Lemont, IL, USA.

Funding

Phase 01 Clinical TrialsZIABC011078 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DOROSHOW, JAMES · 2009 to 2025
$9.0M
CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

backgroundThe National Cancer Institute drug pair screening effort against 60 well-characterized human tumor cell lines (NCI-60) presents an unprecedented resource for modeling combinational drug activity.

resultsWe present a computational model for predicting cell line response to a subset of drug pairs in the NCI-ALMANAC database. Based on residual neural networks for encoding features as well as predicting tumor growth, our model explains 94% of the response variance. While our best result is achieved with a combination of molecular feature types (gene expression, microRNA and proteome), we show that most of the predictive power comes from drug descriptors. To further demonstrate value in detecting anticancer therapy, we rank the drug pairs for each cell line based on model predicted combination effect and recover 80% of the top pairs with enhanced activity.

conclusionsWe present promising results in applying deep learning to predicting combinational drug response. Our feature analysis indicates screening data involving more cell lines are needed for the models to make better use of molecular features.

Indexed as

Cell Line, TumorDeep LearningDrug Evaluation, PreclinicalHumansNational Cancer Institute (U.S.)Neural Networks, ComputerUnited StatesCombination therapyDeep learningin silico drug screeningMachine learning

Identifiers

PMID30577754
PMCPMC6302446

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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.