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Circulating Bacterial DNA as Plasma Biomarkers for Lung Cancer Early Detection

SIMPLE SUMMARY: Pathogenic bacteria play a crucial role in tumor development. Our study analyzed the presence of bacteria related to lung cancer in lung tumors, normal lung tissues, and plasma from lung cancer patients. Three bacteria (Selenomonas, Streptococcus, and Veillonella) showed consistent c...

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Autores principales: Zhou, Huifen, Liao, Jipei, Leng, Qixin, Chinthalapally, Molangur, Dhilipkannah, Pushpa, Jiang, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10058358/
https://www.ncbi.nlm.nih.gov/pubmed/36985157
http://dx.doi.org/10.3390/microorganisms11030582
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author Zhou, Huifen
Liao, Jipei
Leng, Qixin
Chinthalapally, Molangur
Dhilipkannah, Pushpa
Jiang, Feng
author_facet Zhou, Huifen
Liao, Jipei
Leng, Qixin
Chinthalapally, Molangur
Dhilipkannah, Pushpa
Jiang, Feng
author_sort Zhou, Huifen
collection PubMed
description SIMPLE SUMMARY: Pathogenic bacteria play a crucial role in tumor development. Our study analyzed the presence of bacteria related to lung cancer in lung tumors, normal lung tissues, and plasma from lung cancer patients. Three bacteria (Selenomonas, Streptococcus, and Veillonella) showed consistent changes in plasma and higher DNA abundances in the plasma of cancer patients compared with healthy controls. The use of these three bacteria as a plasma biomarker panel can identify lung cancer, regardless of histology and stage. Our findings were validated in additional clinical specimens, demonstrating the potential of circulating bacterial DNA as plasma biomarkers for lung cancer. ABSTRACT: Lung cancer is a leading cause of cancer deaths and early diagnosis can significantly improve outcomes. Pathogenic bacteria have been shown to play a role in tumorigenesis and its analysis provides a new approach for cancer diagnosis. To evaluate the potential of bacteria as plasma biomarkers for early lung cancer detection, we analyzed eight lung-cancer-related bacterial genera in 58 lung cancer patients and 58 controls using ddPCR. Our results showed that five genera had higher DNA abundance in lung tumor tissues compared with normal tissues. Three of these genera (Selenomonas, Streptococcus, and Veillonella) displayed consistent changes in plasma, with higher DNA abundance in lung cancer patients compared with controls. When used as a panel, these three bacterial genera had a sensitivity of 75% and specificity of 78% for lung cancer detection, regardless of stage or histology. The performance of this biomarker panel was confirmed in an independent cohort of 93 lung cancer cases and 93 controls. Thus, circulating bacterial DNA has the potential to be used as plasma biomarkers for early lung cancer detection.
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spelling pubmed-100583582023-03-30 Circulating Bacterial DNA as Plasma Biomarkers for Lung Cancer Early Detection Zhou, Huifen Liao, Jipei Leng, Qixin Chinthalapally, Molangur Dhilipkannah, Pushpa Jiang, Feng Microorganisms Article SIMPLE SUMMARY: Pathogenic bacteria play a crucial role in tumor development. Our study analyzed the presence of bacteria related to lung cancer in lung tumors, normal lung tissues, and plasma from lung cancer patients. Three bacteria (Selenomonas, Streptococcus, and Veillonella) showed consistent changes in plasma and higher DNA abundances in the plasma of cancer patients compared with healthy controls. The use of these three bacteria as a plasma biomarker panel can identify lung cancer, regardless of histology and stage. Our findings were validated in additional clinical specimens, demonstrating the potential of circulating bacterial DNA as plasma biomarkers for lung cancer. ABSTRACT: Lung cancer is a leading cause of cancer deaths and early diagnosis can significantly improve outcomes. Pathogenic bacteria have been shown to play a role in tumorigenesis and its analysis provides a new approach for cancer diagnosis. To evaluate the potential of bacteria as plasma biomarkers for early lung cancer detection, we analyzed eight lung-cancer-related bacterial genera in 58 lung cancer patients and 58 controls using ddPCR. Our results showed that five genera had higher DNA abundance in lung tumor tissues compared with normal tissues. Three of these genera (Selenomonas, Streptococcus, and Veillonella) displayed consistent changes in plasma, with higher DNA abundance in lung cancer patients compared with controls. When used as a panel, these three bacterial genera had a sensitivity of 75% and specificity of 78% for lung cancer detection, regardless of stage or histology. The performance of this biomarker panel was confirmed in an independent cohort of 93 lung cancer cases and 93 controls. Thus, circulating bacterial DNA has the potential to be used as plasma biomarkers for early lung cancer detection. MDPI 2023-02-25 /pmc/articles/PMC10058358/ /pubmed/36985157 http://dx.doi.org/10.3390/microorganisms11030582 Text en © 2023 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
Zhou, Huifen
Liao, Jipei
Leng, Qixin
Chinthalapally, Molangur
Dhilipkannah, Pushpa
Jiang, Feng
Circulating Bacterial DNA as Plasma Biomarkers for Lung Cancer Early Detection
title Circulating Bacterial DNA as Plasma Biomarkers for Lung Cancer Early Detection
title_full Circulating Bacterial DNA as Plasma Biomarkers for Lung Cancer Early Detection
title_fullStr Circulating Bacterial DNA as Plasma Biomarkers for Lung Cancer Early Detection
title_full_unstemmed Circulating Bacterial DNA as Plasma Biomarkers for Lung Cancer Early Detection
title_short Circulating Bacterial DNA as Plasma Biomarkers for Lung Cancer Early Detection
title_sort circulating bacterial dna as plasma biomarkers for lung cancer early detection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10058358/
https://www.ncbi.nlm.nih.gov/pubmed/36985157
http://dx.doi.org/10.3390/microorganisms11030582
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