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- Publisher Website: 10.1021/acscentsci.4c02164
- Scopus: eid_2-s2.0-105003573492
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Article: Electric-Field Molecular Fingerprinting to Probe Cancer
| Title | Electric-Field Molecular Fingerprinting to Probe Cancer |
|---|---|
| Authors | Kepesidis, Kosmas V.Jacob, PhilipSchweinberger, WolfgangHuber, MarinusFeiler, NicoFleischmann, FrankTrubetskov, MichaelVoronina, LiudmilaAschauer, JacquelineEissa, TarekGigou, LeaKarandušovsky, PatrikPupeza, IoachimWeigel, AlexanderAzzeer, AbdallahStief, Christian G.Chaloupka, MichaelReinmuth, NielsBehr, JürgenKolben, ThomasHarbeck, NadiaReiser, MaximilianKrausz, FerencŽigman, Mihaela |
| Issue Date | 2025 |
| Citation | ACS Central Science, 2025, v. 11, n. 4, p. 560-573 How to Cite? |
| Abstract | Human 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 Identifier | http://hdl.handle.net/10722/364393 |
| ISSN | 2023 Impact Factor: 12.7 2023 SCImago Journal Rankings: 3.722 |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kepesidis, Kosmas V. | - |
| dc.contributor.author | Jacob, Philip | - |
| dc.contributor.author | Schweinberger, Wolfgang | - |
| dc.contributor.author | Huber, Marinus | - |
| dc.contributor.author | Feiler, Nico | - |
| dc.contributor.author | Fleischmann, Frank | - |
| dc.contributor.author | Trubetskov, Michael | - |
| dc.contributor.author | Voronina, Liudmila | - |
| dc.contributor.author | Aschauer, Jacqueline | - |
| dc.contributor.author | Eissa, Tarek | - |
| dc.contributor.author | Gigou, Lea | - |
| dc.contributor.author | Karandušovsky, Patrik | - |
| dc.contributor.author | Pupeza, Ioachim | - |
| dc.contributor.author | Weigel, Alexander | - |
| dc.contributor.author | Azzeer, Abdallah | - |
| dc.contributor.author | Stief, Christian G. | - |
| dc.contributor.author | Chaloupka, Michael | - |
| dc.contributor.author | Reinmuth, Niels | - |
| dc.contributor.author | Behr, Jürgen | - |
| dc.contributor.author | Kolben, Thomas | - |
| dc.contributor.author | Harbeck, Nadia | - |
| dc.contributor.author | Reiser, Maximilian | - |
| dc.contributor.author | Krausz, Ferenc | - |
| dc.contributor.author | Žigman, Mihaela | - |
| dc.date.accessioned | 2025-10-30T08:33:25Z | - |
| dc.date.available | 2025-10-30T08:33:25Z | - |
| dc.date.issued | 2025 | - |
| dc.identifier.citation | ACS Central Science, 2025, v. 11, n. 4, p. 560-573 | - |
| dc.identifier.issn | 2374-7943 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/364393 | - |
| dc.description.abstract | Human 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.language | eng | - |
| dc.relation.ispartof | ACS Central Science | - |
| dc.title | Electric-Field Molecular Fingerprinting to Probe Cancer | - |
| dc.type | Article | - |
| dc.description.nature | link_to_subscribed_fulltext | - |
| dc.identifier.doi | 10.1021/acscentsci.4c02164 | - |
| dc.identifier.scopus | eid_2-s2.0-105003573492 | - |
| dc.identifier.volume | 11 | - |
| dc.identifier.issue | 4 | - |
| dc.identifier.spage | 560 | - |
| dc.identifier.epage | 573 | - |
| dc.identifier.eissn | 2374-7951 | - |
