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Comparison of whole blood and serum samples of breast cancer based on laser-induced breakdown spectroscopy with machine learning

To identify cancer from non-cancer is one of the most challenging issues nowadays in the early diagnosis of cancer. The primary issue of early detection is to choose a suitable type of sample collection to diagnose cancer. A comparison of whole blood and serum samples of breast cancer was studied us...

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Autores principales: Idrees, Bushra Sana, Teng, Geer, Israr, Ayesha, Zaib, Huma, Jamil, Yasir, Bilal, Muhammad, Bashir, Sajid, Khan, M. Nouman, Wang, Qianqian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optica Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278612/
https://www.ncbi.nlm.nih.gov/pubmed/37342687
http://dx.doi.org/10.1364/BOE.489513
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author Idrees, Bushra Sana
Teng, Geer
Israr, Ayesha
Zaib, Huma
Jamil, Yasir
Bilal, Muhammad
Bashir, Sajid
Khan, M. Nouman
Wang, Qianqian
author_facet Idrees, Bushra Sana
Teng, Geer
Israr, Ayesha
Zaib, Huma
Jamil, Yasir
Bilal, Muhammad
Bashir, Sajid
Khan, M. Nouman
Wang, Qianqian
author_sort Idrees, Bushra Sana
collection PubMed
description To identify cancer from non-cancer is one of the most challenging issues nowadays in the early diagnosis of cancer. The primary issue of early detection is to choose a suitable type of sample collection to diagnose cancer. A comparison of whole blood and serum samples of breast cancer was studied using laser-induced breakdown spectroscopy (LIBS) with machine learning methods. For LIBS spectra measurement, blood samples were dropped on a substrate of boric acid. For the discrimination of breast cancer and non-cancer samples, eight machine learning models were applied to LIBS spectral data, including decision tree, discrimination analysis, logistic regression, naïve byes, support vector machine, k-nearest neighbor, ensemble and neural networks classifiers. Discrimination between whole blood samples showed that narrow neural networks and trilayer neural networks both provided 91.7% highest prediction accuracy and serum samples showed that all the decision tree models provided 89.7% highest prediction accuracy. However, using whole blood as sample achieved the strong emission lines of spectra, better discrimination results of PCA and maximum prediction accuracy of machine learning models as compared to using serum samples. These merits concluded that whole blood samples could be a good option for the rapid detection of breast cancer. This preliminary research may provide the complementary method for early detection of breast cancer.
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spelling pubmed-102786122023-06-20 Comparison of whole blood and serum samples of breast cancer based on laser-induced breakdown spectroscopy with machine learning Idrees, Bushra Sana Teng, Geer Israr, Ayesha Zaib, Huma Jamil, Yasir Bilal, Muhammad Bashir, Sajid Khan, M. Nouman Wang, Qianqian Biomed Opt Express Article To identify cancer from non-cancer is one of the most challenging issues nowadays in the early diagnosis of cancer. The primary issue of early detection is to choose a suitable type of sample collection to diagnose cancer. A comparison of whole blood and serum samples of breast cancer was studied using laser-induced breakdown spectroscopy (LIBS) with machine learning methods. For LIBS spectra measurement, blood samples were dropped on a substrate of boric acid. For the discrimination of breast cancer and non-cancer samples, eight machine learning models were applied to LIBS spectral data, including decision tree, discrimination analysis, logistic regression, naïve byes, support vector machine, k-nearest neighbor, ensemble and neural networks classifiers. Discrimination between whole blood samples showed that narrow neural networks and trilayer neural networks both provided 91.7% highest prediction accuracy and serum samples showed that all the decision tree models provided 89.7% highest prediction accuracy. However, using whole blood as sample achieved the strong emission lines of spectra, better discrimination results of PCA and maximum prediction accuracy of machine learning models as compared to using serum samples. These merits concluded that whole blood samples could be a good option for the rapid detection of breast cancer. This preliminary research may provide the complementary method for early detection of breast cancer. Optica Publishing Group 2023-05-03 /pmc/articles/PMC10278612/ /pubmed/37342687 http://dx.doi.org/10.1364/BOE.489513 Text en Published by Optica Publishing Group under the terms of the Creative Commons Attribution 4.0 License. Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI. https://creativecommons.org/licenses/by/4.0/https://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Idrees, Bushra Sana
Teng, Geer
Israr, Ayesha
Zaib, Huma
Jamil, Yasir
Bilal, Muhammad
Bashir, Sajid
Khan, M. Nouman
Wang, Qianqian
Comparison of whole blood and serum samples of breast cancer based on laser-induced breakdown spectroscopy with machine learning
title Comparison of whole blood and serum samples of breast cancer based on laser-induced breakdown spectroscopy with machine learning
title_full Comparison of whole blood and serum samples of breast cancer based on laser-induced breakdown spectroscopy with machine learning
title_fullStr Comparison of whole blood and serum samples of breast cancer based on laser-induced breakdown spectroscopy with machine learning
title_full_unstemmed Comparison of whole blood and serum samples of breast cancer based on laser-induced breakdown spectroscopy with machine learning
title_short Comparison of whole blood and serum samples of breast cancer based on laser-induced breakdown spectroscopy with machine learning
title_sort comparison of whole blood and serum samples of breast cancer based on laser-induced breakdown spectroscopy with machine learning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278612/
https://www.ncbi.nlm.nih.gov/pubmed/37342687
http://dx.doi.org/10.1364/BOE.489513
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