Evidence map›Paper›PMID 35601606›Full record

ArticleOncotarget2022

CancerOmicsNet: a multi-omics network-based approach to anti-cancer drug profiling.

Limeng Pu, Manali Singha, Jagannathan Ramanujam, Michal Brylinski

Abstract read
In one paragraph

Article in Oncotarget, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Cancer pharmacoinformatics: Databases and analytical tools.Functional & integrative genomics · 2024
    Review
  5. Article
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  7. Review
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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

4 authors.

Limeng PuCenter for Computation and Technology, Louisiana State University, Baton Rouge, LA 70803, USA.
Manali SinghaDepartment of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.
Jagannathan RamanujamCenter for Computation and Technology, Louisiana State University, Baton Rouge, LA 70803, USA.
Michal BrylinskiCenter for Computation and Technology, Louisiana State University, Baton Rouge, LA 70803, USA.

Funding

Combining structure-based network biology and heterogeneous computing for rational drug repositioning and polypharmacologyR35GM119524 · NIGMS · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI BRYLINSKI, MICHAL · 2016 to 2020
$962k
NIGMS NIH HHS R35 GM119524
6 · The paper itself

Abstract

Development of novel anti-cancer treatments requires not only a comprehensive knowledge of cancer processes and drug mechanisms of action, but also the ability to accurately predict the response of various cancer cell lines to therapeutics. Numerous computational methods have been developed to address this issue, including algorithms employing supervised machine learning. Nonetheless, high prediction accuracies reported for many of these techniques may result from a significant overlap among training, validation, and testing sets, making existing predictors inapplicable to new data. To address these issues, we developed CancerOmicsNet, a graph neural network with sophisticated attention propagation mechanisms to predict the therapeutic effects of kinase inhibitors across various tumors. Emphasizing on the system-level complexity of cancer, CancerOmicsNet integrates multiple heterogeneous data, such as biological networks, genomics, inhibitor profiling, and gene-disease associations, into a unified graph structure. The performance of CancerOmicsNet, properly cross-validated at the tissue level, is 0.83 in terms of the area under the receiver operating characteristics, which is notably higher than those measured for other approaches. CancerOmicsNet generalizes well to unseen data, i.e., it can predict therapeutic effects across a variety of cancer cell lines and inhibitors. CancerOmicsNet is freely available to the academic community at https://github.com/pulimeng/CancerOmicsNet.

Indexed as

Antineoplastic AgentsNeoplasmsAlgorithmsComputational BiologyGenomicsHumansNeural Networks, ComputerAntineoplastic Agentscancer growth ratecancer-specific networksdifferential gene expressiongene-disease associationkinase inhibitors

Identifiers

PMID35601606
PMCPMC9119687

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.