Evidence map›Paper›PMID 35163005›Full record

ArticleInternational journal of molecular sciences2022

Pan-Cancer Prediction of Cell-Line Drug Sensitivity Using Network-Based Methods.

Maryam Pouryahya, Jung Hun Oh, James C Mathews, Zehor Belkhatir, Caroline Moosmüller, Joseph O Deasy, Allen R Tannenbaum

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  3. Molecular Pharmacology at the Crossroads of Precision Medicine.Current issues in molecular biology · 2025
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  13. Progress of the "Molecular Informatics" Section in 2022.International journal of molecular sciences · 2023
    Article
  14. Review
  15. Article
  16. 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

7 authors at 4 institutions in 2 countries.

Maryam PouryahyaDepartment of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Jung Hun OhDepartment of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.ORCID 0000-0001-8791-2755
James C MathewsDepartment of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Zehor BelkhatirSchool of Engineering and Sustainable Development, De Montfort University, Leicester LE1 9BH, UK.ORCID 0000-0001-7277-3895
Caroline MoosmüllerDepartment of Mathematics, University of California at San Diego, La Jolla, CA 92093, USA.ORCID 0000-0002-7728-0261
Joseph O DeasyDepartment of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Allen R TannenbaumDepartments of Computer Science and Applied Mathematics & Statistics, Stony Brook University, Stony Brook, NY 11794, USA.
Memorial Sloan Kettering Cancer Center · USApplied Mathematics (United States) · USDe Montfort University · GBUniversity of California San Diego · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Glymphatic function in a transgenic rat model of Alzheimer's diseaseR01AG048769 · NIA · UNIVERSITY OF ROCHESTER · PI BENVENISTE, HELENE D, NEDERGAARD, MAIKEN · 2014 to 2018
$1.4M
Radiotherapy-associated breast cancer: machine learning on genotypes to predict individualized riskR21CA234752 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI BERNSTEIN, JONINE L., OH, JUNG HUN · 2020 to 2021
$462k
NCI NIH HHS P30 CA008748NCI NIH HHS R21 CA234752NIH HHS P30 CA008748NIH HHS R01 AG048769NIH HHS R21 CA234752
6 · The paper itself

Abstract

The development of reliable predictive models for individual cancer cell lines to identify an optimal cancer drug is a crucial step to accelerate personalized medicine, but vast differences in cancer cell lines and drug characteristics make it quite challenging to develop predictive models that result in high predictive power and explain the similarity of cell lines or drugs. Our study proposes a novel network-based methodology that breaks the problem into smaller, more interpretable problems to improve the predictive power of anti-cancer drug responses in cell lines. For the drug-sensitivity study, we used the GDSC database for 915 cell lines and 200 drugs. The theory of optimal mass transport was first used to separately cluster cell lines and drugs, using gene-expression profiles and extensive cheminformatic drug features, represented in a form of data networks. To predict cell-line specific drug responses, random forest regression modeling was separately performed for each cell-line drug cluster pair. Post-modeling biological analysis was further performed to identify potential biological correlates associated with drug responses. The network-based clustering method resulted in 30 distinct cell-line drug cluster pairs. Predictive modeling on each cell-line-drug cluster outperformed alternative computational methods in predicting drug responses. We found that among the four drugs top-ranked with respect to prediction performance, three targeted the PI3K/mTOR signaling pathway. Predictive modeling on clustered subsets of cell lines and drugs improved the prediction accuracy of cell-line specific drug responses. Post-modeling analysis identified plausible biological processes associated with drug responses.

Indexed as

Antineoplastic AgentsCell Line, TumorCheminformaticsDrug Screening Assays, AntitumorGene Regulatory NetworksHumansNeoplasmsPhosphatidylinositol 3-KinasesRegression AnalysisSignal TransductionTOR Serine-Threonine KinasesAntineoplastic AgentsMTOR protein, humanPhosphatidylinositol 3-KinasesTOR Serine-Threonine Kinasescell linesdrug sensitivitynetwork-based clusteringoptimal mass transport

Identifiers

PMID35163005
PMCPMC8835038
OpenAlexW4205500224

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.