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SERS Liquid Biopsy Profiling of Serum for the Diagnosis of Kidney Cancer

Renal cancer (RC) represents 3% of all cancers, with a 2% annual increase in incidence worldwide, opening the discussion about the need for screening. However, no established screening tool currently exists for RC. To tackle this issue, we assessed surface-enhanced Raman scattering (SERS) profiling...

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Autores principales: Moisoiu, Tudor, Iancu, Stefania D., Burghelea, Dan, Dragomir, Mihnea P., Iacob, Gheorghita, Stefancu, Andrei, Cozan, Ramona G., Antal, Oana, Bálint, Zoltán, Muntean, Valentin, Badea, Radu I., Licarete, Emilia, Leopold, Nicolae, Elec, Florin I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8869590/
https://www.ncbi.nlm.nih.gov/pubmed/35203443
http://dx.doi.org/10.3390/biomedicines10020233
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author Moisoiu, Tudor
Iancu, Stefania D.
Burghelea, Dan
Dragomir, Mihnea P.
Iacob, Gheorghita
Stefancu, Andrei
Cozan, Ramona G.
Antal, Oana
Bálint, Zoltán
Muntean, Valentin
Badea, Radu I.
Licarete, Emilia
Leopold, Nicolae
Elec, Florin I.
author_facet Moisoiu, Tudor
Iancu, Stefania D.
Burghelea, Dan
Dragomir, Mihnea P.
Iacob, Gheorghita
Stefancu, Andrei
Cozan, Ramona G.
Antal, Oana
Bálint, Zoltán
Muntean, Valentin
Badea, Radu I.
Licarete, Emilia
Leopold, Nicolae
Elec, Florin I.
author_sort Moisoiu, Tudor
collection PubMed
description Renal cancer (RC) represents 3% of all cancers, with a 2% annual increase in incidence worldwide, opening the discussion about the need for screening. However, no established screening tool currently exists for RC. To tackle this issue, we assessed surface-enhanced Raman scattering (SERS) profiling of serum as a liquid biopsy strategy to detect renal cell carcinoma (RCC), the most prevalent histologic subtype of RC. Thus, serum samples were collected from 23 patients with RCC and 27 controls (CTRL) presenting with a benign urological pathology such as lithiasis or benign prostatic hypertrophy. SERS profiling of deproteinized serum yielded SERS band spectra attributed mainly to purine metabolites, which exhibited higher intensities in the RCC group, and Raman bands of carotenoids, which exhibited lower intensities in the RCC group. Principal component analysis (PCA) of the SERS spectra showed a tendency for the unsupervised clustering of the two groups. Next, three machine learning algorithms (random forest, kNN, naïve Bayes) were implemented as supervised classification algorithms for achieving discrimination between the RCC and CTRL groups, yielding an AUC of 0.78 for random forest, 0.78 for kNN, and 0.76 for naïve Bayes (average AUC 0.77 ± 0.01). The present study highlights the potential of SERS liquid biopsy as a diagnostic and screening strategy for RCC. Further studies involving large cohorts and other urologic malignancies as controls are needed to validate the proposed SERS approach.
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spelling pubmed-88695902022-02-25 SERS Liquid Biopsy Profiling of Serum for the Diagnosis of Kidney Cancer Moisoiu, Tudor Iancu, Stefania D. Burghelea, Dan Dragomir, Mihnea P. Iacob, Gheorghita Stefancu, Andrei Cozan, Ramona G. Antal, Oana Bálint, Zoltán Muntean, Valentin Badea, Radu I. Licarete, Emilia Leopold, Nicolae Elec, Florin I. Biomedicines Article Renal cancer (RC) represents 3% of all cancers, with a 2% annual increase in incidence worldwide, opening the discussion about the need for screening. However, no established screening tool currently exists for RC. To tackle this issue, we assessed surface-enhanced Raman scattering (SERS) profiling of serum as a liquid biopsy strategy to detect renal cell carcinoma (RCC), the most prevalent histologic subtype of RC. Thus, serum samples were collected from 23 patients with RCC and 27 controls (CTRL) presenting with a benign urological pathology such as lithiasis or benign prostatic hypertrophy. SERS profiling of deproteinized serum yielded SERS band spectra attributed mainly to purine metabolites, which exhibited higher intensities in the RCC group, and Raman bands of carotenoids, which exhibited lower intensities in the RCC group. Principal component analysis (PCA) of the SERS spectra showed a tendency for the unsupervised clustering of the two groups. Next, three machine learning algorithms (random forest, kNN, naïve Bayes) were implemented as supervised classification algorithms for achieving discrimination between the RCC and CTRL groups, yielding an AUC of 0.78 for random forest, 0.78 for kNN, and 0.76 for naïve Bayes (average AUC 0.77 ± 0.01). The present study highlights the potential of SERS liquid biopsy as a diagnostic and screening strategy for RCC. Further studies involving large cohorts and other urologic malignancies as controls are needed to validate the proposed SERS approach. MDPI 2022-01-22 /pmc/articles/PMC8869590/ /pubmed/35203443 http://dx.doi.org/10.3390/biomedicines10020233 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Moisoiu, Tudor
Iancu, Stefania D.
Burghelea, Dan
Dragomir, Mihnea P.
Iacob, Gheorghita
Stefancu, Andrei
Cozan, Ramona G.
Antal, Oana
Bálint, Zoltán
Muntean, Valentin
Badea, Radu I.
Licarete, Emilia
Leopold, Nicolae
Elec, Florin I.
SERS Liquid Biopsy Profiling of Serum for the Diagnosis of Kidney Cancer
title SERS Liquid Biopsy Profiling of Serum for the Diagnosis of Kidney Cancer
title_full SERS Liquid Biopsy Profiling of Serum for the Diagnosis of Kidney Cancer
title_fullStr SERS Liquid Biopsy Profiling of Serum for the Diagnosis of Kidney Cancer
title_full_unstemmed SERS Liquid Biopsy Profiling of Serum for the Diagnosis of Kidney Cancer
title_short SERS Liquid Biopsy Profiling of Serum for the Diagnosis of Kidney Cancer
title_sort sers liquid biopsy profiling of serum for the diagnosis of kidney cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8869590/
https://www.ncbi.nlm.nih.gov/pubmed/35203443
http://dx.doi.org/10.3390/biomedicines10020233
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