Evidence map›Paper›PMID 25232952›Full record

ArticlePLoS computational biology2014

A systems approach to predict oncometabolites via context-specific genome-scale metabolic networks.

Hojung Nam, Miguel Campodonico, Aarash Bordbar, Daniel R Hyduke, Sangwoo Kim, Daniel C Zielinski, Bernhard O Palsson

Abstract read
In one paragraph

Article in PLoS computational biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed.

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  5. Genome-scale models in human metabologenomics.Nature reviews. Genetics · 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

7 authors.

Hojung NamDepartment of Bioengineering, University of California San Diego, La Jolla, California, United States of America; School of Information & Communications, Gwangju Institute of Science and Technology (GIST), Buk-gu, Gwangju, Republic of Korea.
Miguel CampodonicoDepartment of Bioengineering, University of California San Diego, La Jolla, California, United States of America; Centre for Biotechnology and Bioengineering, CeBiB, University of Chile, Santiago, Chile.
Aarash BordbarDepartment of Bioengineering, University of California San Diego, La Jolla, California, United States of America.
Daniel R HydukeDepartment of Bioengineering, University of California San Diego, La Jolla, California, United States of America.
Sangwoo KimSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seodaemun-gu, Seoul, South Korea.
Daniel C ZielinskiDepartment of Bioengineering, University of California San Diego, La Jolla, California, United States of America.
Bernhard O PalssonDepartment of Bioengineering, University of California San Diego, La Jolla, California, United States of America; Department of Pediatrics, University of California San Diego, La Jolla, California, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Altered metabolism in cancer cells has been viewed as a passive response required for a malignant transformation. However, this view has changed through the recently described metabolic oncogenic factors: mutated isocitrate dehydrogenases (IDH), succinate dehydrogenase (SDH), and fumarate hydratase (FH) that produce oncometabolites that competitively inhibit epigenetic regulation. In this study, we demonstrate in silico predictions of oncometabolites that have the potential to dysregulate epigenetic controls in nine types of cancer by incorporating massive scale genetic mutation information (collected from more than 1,700 cancer genomes), expression profiling data, and deploying Recon 2 to reconstruct context-specific genome-scale metabolic models. Our analysis predicted 15 compounds and 24 substructures of potential oncometabolites that could result from the loss-of-function and gain-of-function mutations of metabolic enzymes, respectively. These results suggest a substantial potential for discovering unidentified oncometabolites in various forms of cancers.

Indexed as

Cell Line, TumorCluster AnalysisComputer SimulationGene Expression ProfilingHumansMetabolic Networks and PathwaysMetabolomeModels, BiologicalMutationNeoplasmsSystems Biology

Identifiers

PMID25232952
PMCPMC4168981

What OpenQuestion holds

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Registered trials

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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.