Evidence map›Paper›PMID 33361798›Full record

ArticleNature protocols2021

OCTAD: an open workspace for virtually screening therapeutics targeting precise cancer patient groups using gene expression features.

Billy Zeng, Benjamin S Glicksberg, Patrick Newbury, Evgeny Chekalin, Jing Xing, Ke Liu, Anita Wen, Caven Chow, Bin Chen

Abstract read
In one paragraph

Article in Nature protocols, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

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  9. AnchorDrug: A system for drug-induced gene expression prediction in new contexts through active learning.Proceedings of the ... SIAM International Conference on Data Mining. SIAM International Conference on Data Mining · 2025
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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

9 authors.

Billy Zeng *Department of Pediatrics and Human Development, Michigan State University, Grand Rapids, MI, USA.
Benjamin S Glicksberg *Bakar Computational Health Sciences Institute, University of California, San Francisco, San Francisco, CA, USA.ORCID http://orcid.org/0000-0003-4515-8090
Patrick Newbury *Department of Pediatrics and Human Development, Michigan State University, Grand Rapids, MI, USA.ORCID http://orcid.org/0000-0002-3756-1747
Evgeny Chekalin *Department of Pediatrics and Human Development, Michigan State University, Grand Rapids, MI, USA.
Jing XingDepartment of Pediatrics and Human Development, Michigan State University, Grand Rapids, MI, USA.
Ke LiuDepartment of Pediatrics and Human Development, Michigan State University, Grand Rapids, MI, USA.
Anita WenDepartment of Nutrition, University of California, Davis, Davis, CA, USA.
Caven ChowBakar Computational Health Sciences Institute, University of California, San Francisco, San Francisco, CA, USA.
Bin ChenDepartment of Pediatrics and Human Development, Michigan State University, Grand Rapids, MI, USA. chenbi12@msu.edu.ORCID http://orcid.org/0000-0001-8858-874X

Funding

Repurpose open data to discover therapeutics for understudied diseasesR01GM134307 · NIGMS · MICHIGAN STATE UNIVERSITY · PI CHEN, BIN · 2019 to 2023
$2.5M
Integrating transcriptomic, proteomic and pharmacogenomic data to inform individualized therapy in cancersK01ES028047 · NIEHS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHEN, BIN · 2017 to 2020
$682k
Targeting glucose metabolism for the treatment of Hepatocellular CarcinomaR21TR001743 · NCATS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHEN, BIN · 2017 to 2018
$560k
NCATS NIH HHS R21 TR001743NIEHS NIH HHS K01 ES028047NIGMS NIH HHS R01 GM134307U.S. Department of Health & Human Services | NIH | National Center for Advancing Translational Sciences (NCATS) R21TR001743U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM134307
6 · The paper itself

Abstract

As the field of precision medicine progresses, treatments for patients with cancer are starting to be tailored to their molecular as well as their clinical features. The emerging cancer subtypes defined by these molecular features require that dedicated resources be used to assist the discovery of drug candidates for preclinical evaluation. Voluminous gene expression profiles of patients with cancer have been accumulated in public databases, enabling the creation of cancer-specific expression signatures. Meanwhile, large-scale gene expression profiles of cellular responses to chemical compounds have also recently became available. By matching the cancer-specific expression signature to compound-induced gene expression profiles from large drug libraries, researchers can prioritize small molecules that present high potency to reverse expression of signature genes for further experimental testing of their efficacy. This approach has proven to be an efficient and cost-effective way to identify efficacious drug candidates. However, the success of this approach requires multiscale procedures, imposing considerable challenges to many labs. To address this, we developed Open Cancer TherApeutic Discovery (OCTAD; http://octad.org ): an open workspace for virtually screening compounds targeting precise groups of patients with cancer using gene expression features. Its database includes 19,127 patient tissue samples covering more than 50 cancer types and expression profiles for 12,442 distinct compounds. The program is used to perform deep-learning-based reference tissue selection, disease gene expression signature creation, drug reversal potency scoring and in silico validation. OCTAD is available as a web portal and a standalone R package to allow experimental and computational scientists to easily navigate the tool.

Indexed as

Biomarkers, PharmacologicalComputer SimulationDatabases, GeneticDrug Screening Assays, AntitumorEarly Detection of CancerGene ExpressionGene Expression ProfilingGene Expression Regulation, NeoplasticHumansNeoplasmsPrecision MedicineTranscriptomeBiomarkers, Pharmacological

Identifiers

PMID33361798
PMCPMC8080884

What OpenQuestion holds

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LicenceTDM
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.