Evidence map›Paper›PMID 33772663›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2021

Discrepancies in metabolomic biomarker identification from patient-derived lung cancer revealed by combined variation in data pre-treatment and imputation methods.

Hunter A Miller, Ramy Emam, Chip M Lynch, Samuel Bockhorst, Hermann B Frieboes

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Article in Metabolomics : Official journal of the Metabolomic Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Hunter A MillerDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY, USA.
Ramy EmamDepartment of Bioengineering, University of Louisville, Louisville, KY, USA.
Chip M LynchDepartment of Computer Engineering and Computer Science, University of Louisville, Louisville, USA.
Samuel BockhorstDepartment of Medicine, University of Louisville, Louisville, USA.
Hermann B FrieboesDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY, USA. hbfrie01@louisville.edu.ORCID http://orcid.org/0000-0001-5959-4286

Funding

Integrated framework to predict chemotherapy response post lung tumor resectionR15CA203605 · NCI · UNIVERSITY OF LOUISVILLE · PI FRIEBOES, HERMANN · 2016 to 2016
$462k
NCI NIH HHS R15 CA203605
6 · The paper itself

Abstract

introductionThe identification of metabolomic biomarkers predictive of cancer patient response to therapy and of disease stage has been pursued as a "holy grail" of modern oncology, relying on the metabolic dysfunction that characterizes cancer progression. In spite of the evaluation of many candidate biomarkers, however, determination of a consistent set with practical clinical utility has proven elusive.

objectiveIn this study, we systematically examine the combined role of data pre-treatment and imputation methods on the performance of multivariate data analysis methods and their identification of potential biomarkers.

methodsUniquely, we are able to systematically evaluate both unsupervised and supervised methods with a metabolomic data set obtained from patient-derived lung cancer core biopsies with true missing values. Eight pre-treatment methods, ten imputation methods, and two data analysis methods were applied in combination.

resultsThe combined choice of pre-treatment and imputation methods is critical in the definition of candidate biomarkers, with deficient or inappropriate selection of these methods leading to inconsistent results, and with important biomarkers either being overlooked or reported as a false positive. The log transformation appeared to normalize the original tumor data most effectively, but the performance of the imputation applied after the transformation was highly dependent on the characteristics of the data set.

conclusionThe combined choice of pre-treatment and imputation methods may need careful evaluation prior to metabolomic data analysis of human tumors, in order to enable consistent identification of potential biomarkers predictive of response to therapy and of disease stage.

Indexed as

BiomarkersData AnalysisHumansLung NeoplasmsMetabolomicsPrincipal Component AnalysisBiomarkersImputation methodsLung cancerMachine learningMetabolomicsMultivariate statistical analysisPre-treatment methods

Identifiers

PMID33772663
PMCPMC8138701

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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.