Evidence map›Paper›PMID 31126892›Full record

ArticleEBioMedicine2019

Identifying and targeting cancer-specific metabolism with network-based drug target prediction.

Maria Pires Pacheco, Tamara Bintener, Dominik Ternes, Dagmar Kulms, Serge Haan, Elisabeth Letellier, Thomas Sauter

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
4.0field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it, 79 citations in OpenAlex.

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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

7 authors at 2 institutions in 2 countries.

Maria Pires PachecoLife Sciences Research Unit, University of Luxembourg, Esch-Alzette, Luxembourg.
Tamara BintenerLife Sciences Research Unit, University of Luxembourg, Esch-Alzette, Luxembourg.
Dominik TernesLife Sciences Research Unit, University of Luxembourg, Esch-Alzette, Luxembourg.
Dagmar KulmsExperimental Dermatology, Department of Dermatology, Technical University Dresden, Dresden, Germany; Center for Regenerative Therapies, Technical University Dresden, Dresden, Germany.
Serge HaanLife Sciences Research Unit, University of Luxembourg, Esch-Alzette, Luxembourg.
Elisabeth LetellierLife Sciences Research Unit, University of Luxembourg, Esch-Alzette, Luxembourg.
Thomas SauterLife Sciences Research Unit, University of Luxembourg, Esch-Alzette, Luxembourg. Electronic address: thomas.sauter@uni.lu.
University of Luxembourg · LUTechnische Universität Dresden · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetabolic rewiring allows cancer cells to sustain high proliferation rates. Thus, targeting only the cancer-specific cellular metabolism will safeguard healthy tissues.

methodsWe developed the very efficient FASTCORMICS RNA-seq workflow (rFASTCORMICS) to build 10,005 high-resolution metabolic models from the TCGA dataset to capture metabolic rewiring strategies in cancer cells. Colorectal cancer (CRC) was used as a test case for a repurposing workflow based on rFASTCORMICS.

findingsAlternative pathways that are not required for proliferation or survival tend to be shut down and, therefore, tumours display cancer-specific essential genes that are significantly enriched for known drug targets. We identified naftifine, ketoconazole, and mimosine as new potential CRC drugs, which were experimentally validated.

interpretationThe here presented rFASTCORMICS workflow successfully reconstructs a metabolic model based on RNA-seq data and successfully predicted drug targets and drugs not yet indicted for colorectal cancer. FUND: This study was supported by the University of Luxembourg (IRP grant scheme; R-AGR-0755-12), the Luxembourg National Research Fund (FNR PRIDE PRIDE15/10675146/CANBIO), the Fondation Cancer (Luxembourg), the European Union's Horizon2020 research and innovation programme under the Marie Sklodowska- Curie grant agreement No 642295 (MEL-PLEX), and the German Federal Ministry of Education and Research (BMBF) within the project MelanomSensitivity (BMBF/BM/7643621).

Indexed as

Biomarkers, TumorComputational BiologyDrug DiscoveryMolecular Targeted TherapyAlgorithmsAntineoplastic AgentsEnergy MetabolismGene DeletionGene Expression ProfilingHumansReproducibility of ResultsWorkflowAntineoplastic AgentsBiomarkers, TumorCancerDrug repurposingMachine learningMetabolic modelling

Identifiers

PMID31126892
PMCPMC6558238
OpenAlexW2944993265

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.