Evidence map›Paper›PMID 31066443›Full record

ArticleNucleic acids research2019

DrugComb: an integrative cancer drug combination data portal.

Bulat Zagidullin, Jehad Aldahdooh, Shuyu Zheng, Wenyu Wang, Yinyin Wang, Joseph Saad, Alina Malyutina, Mohieddin Jafari, Ziaurrehman Tanoli, Alberto Pessia and 1 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 142 papers.

0numbers the graph read from it
0cells of the map it votes in
142citing 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

142 citing papers in PubMed.

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82 more citing papers are in PubMed but not listed here.

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

11 authors.

Bulat ZagidullinInstitute for Molecular Medicine Finland, Helsinki Life Science Institute, University of Helsinki, Finland.
Jehad AldahdoohInstitute for Molecular Medicine Finland, Helsinki Life Science Institute, University of Helsinki, Finland.
Shuyu ZhengInstitute for Molecular Medicine Finland, Helsinki Life Science Institute, University of Helsinki, Finland.
Wenyu WangInstitute for Molecular Medicine Finland, Helsinki Life Science Institute, University of Helsinki, Finland.
Yinyin WangInstitute for Molecular Medicine Finland, Helsinki Life Science Institute, University of Helsinki, Finland.
Joseph SaadInstitute for Molecular Medicine Finland, Helsinki Life Science Institute, University of Helsinki, Finland.
Alina MalyutinaInstitute for Molecular Medicine Finland, Helsinki Life Science Institute, University of Helsinki, Finland.
Mohieddin JafariInstitute for Molecular Medicine Finland, Helsinki Life Science Institute, University of Helsinki, Finland.
Ziaurrehman TanoliInstitute for Molecular Medicine Finland, Helsinki Life Science Institute, University of Helsinki, Finland.
Alberto PessiaInstitute for Molecular Medicine Finland, Helsinki Life Science Institute, University of Helsinki, Finland.
Jing TangInstitute for Molecular Medicine Finland, Helsinki Life Science Institute, University of Helsinki, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug combination therapy has the potential to enhance efficacy, reduce dose-dependent toxicity and prevent the emergence of drug resistance. However, discovery of synergistic and effective drug combinations has been a laborious and often serendipitous process. In recent years, identification of combination therapies has been accelerated due to the advances in high-throughput drug screening, but informatics approaches for systems-level data management and analysis are needed. To contribute toward this goal, we created an open-access data portal called DrugComb (https://drugcomb.fimm.fi) where the results of drug combination screening studies are accumulated, standardized and harmonized. Through the data portal, we provided a web server to analyze and visualize users' own drug combination screening data. The users can also effectively participate a crowdsourcing data curation effect by depositing their data at DrugComb. To initiate the data repository, we collected 437 932 drug combinations tested on a variety of cancer cell lines. We showed that linear regression approaches, when considering chemical fingerprints as predictors, have the potential to achieve high accuracy of predicting the sensitivity of drug combinations. All the data and informatics tools are freely available in DrugComb to enable a more efficient utilization of data resources for future drug combination discovery.

Indexed as

Drug SynergismAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsComputational BiologyDrug DiscoveryDrug Evaluation, PreclinicalHumansNeoplasmsAntineoplastic Agents

Identifiers

PMID31066443
PMCPMC6602441

What OpenQuestion holds

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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.