Evidence map›Paper›PMID 26225227›Full record

ArticleCPT: pharmacometrics & systems pharmacology2015

DIGRE: Drug-Induced Genomic Residual Effect Model for Successful Prediction of Multidrug Effects.

J Yang, H Tang, Y Li, R Zhong, T Wang, Stc Wong, G Xiao, Y Xie

Open access · goldAbstract read
In one paragraph

Article in CPT: pharmacometrics & systems pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 39 citations in OpenAlex.

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  5. Anticancer drug synergy prediction in understudied tissues using transfer learning.Journal of the American Medical Informatics Association : JAMIA · 2021
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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

8 authors at 3 institutions in 2 countries.

J YangDepartment of Clinical Sciences, Quantitative Biomedical Research Center, University of Texas Southwestern Medical Center Dallas, Texas, USA.
H TangDepartment of Clinical Sciences, Quantitative Biomedical Research Center, University of Texas Southwestern Medical Center Dallas, Texas, USA.
Y LiDepartment of Immunology, University of Texas Southwestern Medical Center Dallas, Texas, USA ; Laboratory of Disease Genomics and Individualized Medicine, Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences Beijing, China.
R ZhongDepartment of Clinical Sciences, Quantitative Biomedical Research Center, University of Texas Southwestern Medical Center Dallas, Texas, USA.
T WangDepartment of Clinical Sciences, Quantitative Biomedical Research Center, University of Texas Southwestern Medical Center Dallas, Texas, USA.
Stc WongDepartment of Systems Medicine and Bioengineering, Houston Methodist Research Institute, Weill Cornell Medical College Houston, Texas, USA.
G XiaoDepartment of Clinical Sciences, Quantitative Biomedical Research Center, University of Texas Southwestern Medical Center Dallas, Texas, USA.
Y XieDepartment of Clinical Sciences, Quantitative Biomedical Research Center, University of Texas Southwestern Medical Center Dallas, Texas, USA ; Simmons Cancer Center, University of Texas Southwestern Medical Center Dallas, Texas, USA.
The University of Texas Southwestern Medical Center · USChinese Academy of Sciences · CNMethodist Hospital · US

Funding

Integrative Analysis to Identify Therapeutic Targets for Lung CancerR01CA172211 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI XIAO, GUANGHUA · 2013 to 2017
$1.6M
Predicting Adjuvant Chemotherapy Response in Lung CancerR01CA152301 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI XIE, YANG · 2010 to 2014
$1.5M
Secondary Data Analyses for Substance Abuse ResearchR33DA027592 · NIDA · UT SOUTHWESTERN MEDICAL CENTER · PI XIAO, GUANGHUA · 2011 to 2012
$622k
NCI NIH HHS R01 CA152301NCI NIH HHS R01 CA172211NIDA NIH HHS R33 DA027592
6 · The paper itself

Abstract

Multidrug regimens are a promising strategy for improving therapeutic efficacy and reducing side effects, especially for complex disorders such as cancer. However, the use of multidrug therapies is very challenging, due to a lack of understanding of the mechanisms of drug interactions. We herein present a novel computational approach-Drug-Induced Genomic Residual Effect (DIGRE) Computational Model-to predict drug combination effects by explicitly modeling drug response curves and gene expression changes after drug treatments. The prediction performance of DIGRE was evaluated using two datasets: (i) OCI-LY3 B-lymphoma cells treated with 14 different drugs and (ii) MCF breast cancer cells treated with combinations of gefitinib and docetaxel at different doses. In both datasets, the predicted drug combination effects significantly correlated with the experimental results. The results indicated the model was useful in predicting drug combination effects, which may greatly facilitate the discovery of new, effective multidrug therapies.

Identifiers

PMID26225227
PMCPMC4360668
OpenAlexW1546436101

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.