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Article: Electric-Field Molecular Fingerprinting to Probe Cancer

TitleElectric-Field Molecular Fingerprinting to Probe Cancer
Authors
Issue Date2025
Citation
ACS Central Science, 2025, v. 11, n. 4, p. 560-573 How to Cite?
AbstractHuman biofluids serve as indicators of various physiological states, and recent advances in molecular profiling technologies hold great potential for enhancing clinical diagnostics. Leveraging recent developments in laser-based electric-field molecular fingerprinting, we assess its potential for in vitro diagnostics. In a proof-of-concept clinical study involving 2533 participants, we conducted randomized measurement campaigns to spectroscopically profile bulk venous blood plasma across lung, prostate, breast, and bladder cancer. Employing machine learning, we detected infrared signatures specific to therapy-naı̈ve cancer states, distinguishing them from matched control individuals with a cross-validation ROC AUC of 0.88 for lung cancer and values ranging from 0.68 to 0.69 for the other three cancer entities. In an independent held-out test data set, designed to reflect different experimental conditions from those used during model training, we achieved a lung cancer detection ROC AUC of 0.81. Our study demonstrates that electric-field molecular fingerprinting is a robust technological framework broadly applicable to disease phenotyping under real-world conditions.
Persistent Identifierhttp://hdl.handle.net/10722/364393
ISSN
2023 Impact Factor: 12.7
2023 SCImago Journal Rankings: 3.722

 

DC FieldValueLanguage
dc.contributor.authorKepesidis, Kosmas V.-
dc.contributor.authorJacob, Philip-
dc.contributor.authorSchweinberger, Wolfgang-
dc.contributor.authorHuber, Marinus-
dc.contributor.authorFeiler, Nico-
dc.contributor.authorFleischmann, Frank-
dc.contributor.authorTrubetskov, Michael-
dc.contributor.authorVoronina, Liudmila-
dc.contributor.authorAschauer, Jacqueline-
dc.contributor.authorEissa, Tarek-
dc.contributor.authorGigou, Lea-
dc.contributor.authorKarandušovsky, Patrik-
dc.contributor.authorPupeza, Ioachim-
dc.contributor.authorWeigel, Alexander-
dc.contributor.authorAzzeer, Abdallah-
dc.contributor.authorStief, Christian G.-
dc.contributor.authorChaloupka, Michael-
dc.contributor.authorReinmuth, Niels-
dc.contributor.authorBehr, Jürgen-
dc.contributor.authorKolben, Thomas-
dc.contributor.authorHarbeck, Nadia-
dc.contributor.authorReiser, Maximilian-
dc.contributor.authorKrausz, Ferenc-
dc.contributor.authorŽigman, Mihaela-
dc.date.accessioned2025-10-30T08:33:25Z-
dc.date.available2025-10-30T08:33:25Z-
dc.date.issued2025-
dc.identifier.citationACS Central Science, 2025, v. 11, n. 4, p. 560-573-
dc.identifier.issn2374-7943-
dc.identifier.urihttp://hdl.handle.net/10722/364393-
dc.description.abstractHuman biofluids serve as indicators of various physiological states, and recent advances in molecular profiling technologies hold great potential for enhancing clinical diagnostics. Leveraging recent developments in laser-based electric-field molecular fingerprinting, we assess its potential for in vitro diagnostics. In a proof-of-concept clinical study involving 2533 participants, we conducted randomized measurement campaigns to spectroscopically profile bulk venous blood plasma across lung, prostate, breast, and bladder cancer. Employing machine learning, we detected infrared signatures specific to therapy-naı̈ve cancer states, distinguishing them from matched control individuals with a cross-validation ROC AUC of 0.88 for lung cancer and values ranging from 0.68 to 0.69 for the other three cancer entities. In an independent held-out test data set, designed to reflect different experimental conditions from those used during model training, we achieved a lung cancer detection ROC AUC of 0.81. Our study demonstrates that electric-field molecular fingerprinting is a robust technological framework broadly applicable to disease phenotyping under real-world conditions.-
dc.languageeng-
dc.relation.ispartofACS Central Science-
dc.titleElectric-Field Molecular Fingerprinting to Probe Cancer-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/acscentsci.4c02164-
dc.identifier.scopuseid_2-s2.0-105003573492-
dc.identifier.volume11-
dc.identifier.issue4-
dc.identifier.spage560-
dc.identifier.epage573-
dc.identifier.eissn2374-7951-

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