Evidence map›Paper›PMID 34205912›Full record

ArticleJournal of personalized medicine2021

Exploring the Metabolic Heterogeneity of Cancers: A Benchmark Study of Context-Specific Models.

Mahdi Jalili, Martin Scharm, Olaf Wolkenhauer, Mehdi Damaghi, Ali Salehzadeh-Yazdi

Abstract read
In one paragraph

Article in Journal of personalized medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

5 authors.

Mahdi JaliliHematology, Oncology and SCT Research Center, Tehran University of Medical Sciences, Tehran 14114, Iran.
Martin ScharmDepartment of Systems Biology and Bioinformatics, University of Rostock, 18051 Rostock, Germany.
Olaf WolkenhauerDepartment of Systems Biology and Bioinformatics, University of Rostock, 18051 Rostock, Germany.
Mehdi DamaghiDepartment of Cancer Physiology, Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.ORCID 0000-0002-7744-6161
Ali Salehzadeh-YazdiDepartment of Systems Biology and Bioinformatics, University of Rostock, 18051 Rostock, Germany.ORCID 0000-0002-1678-0051

Funding

Bundesministerium für Bildung und Forschung SASKit project (FKZ 01ZX1903A)
6 · The paper itself

Abstract

Metabolic heterogeneity is a hallmark of cancer and can distinguish a normal phenotype from a cancer phenotype. In the systems biology domain, context-specific models facilitate extracting physiologically relevant information from high-quality data. Here, to utilize the heterogeneity of metabolic patterns to discover biomarkers of all cancers, we benchmarked thousands of context-specific models using well-established algorithms for the integration of omics data into the generic human metabolic model Recon3D. By analyzing the active reactions capable of carrying flux and their magnitude through flux balance analysis, we proved that the metabolic pattern of each cancer is unique and could act as a cancer metabolic fingerprint. Subsequently, we searched for proper feature selection methods to cluster the flux states characterizing each cancer. We employed PCA-based dimensionality reduction and a random forest learning algorithm to reveal reactions containing the most relevant information in order to effectively identify the most influential fluxes. Conclusively, we discovered different pathways that are probably the main sources for metabolic heterogeneity in cancers. We designed the GEMbench website to interactively present the data, methods, and analysis results.

Indexed as

cancer metabolismdata integrationFBA-based featuregenome-scale metabolic modelmetabolic patternWarburg effect

Identifiers

PMID34205912
PMCPMC8229374

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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.