Cargando…
Gut mycobiome as a potential non-invasive tool in early detection of lung adenocarcinoma: a cross-sectional study
BACKGROUND: The gut mycobiome of patients with lung adenocarcinoma (LUAD) remains unexplored. This study aimed to characterize the gut mycobiome in patients with LUAD and evaluate the potential of gut fungi as non-invasive biomarkers for early diagnosis. METHODS: In total, 299 fecal samples from Bei...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617124/ https://www.ncbi.nlm.nih.gov/pubmed/37904139 http://dx.doi.org/10.1186/s12916-023-03095-z |
_version_ | 1785129537860796416 |
---|---|
author | Liu, Qingyan Zhang, Weidong Pei, Yanbin Tao, Haitao Ma, Junxun Li, Rong Zhang, Fan Wang, Lijie Shen, Leilei Liu, Yang Jia, Xiaodong Hu, Yi |
author_facet | Liu, Qingyan Zhang, Weidong Pei, Yanbin Tao, Haitao Ma, Junxun Li, Rong Zhang, Fan Wang, Lijie Shen, Leilei Liu, Yang Jia, Xiaodong Hu, Yi |
author_sort | Liu, Qingyan |
collection | PubMed |
description | BACKGROUND: The gut mycobiome of patients with lung adenocarcinoma (LUAD) remains unexplored. This study aimed to characterize the gut mycobiome in patients with LUAD and evaluate the potential of gut fungi as non-invasive biomarkers for early diagnosis. METHODS: In total, 299 fecal samples from Beijing, Suzhou, and Hainan were collected prospectively. Using internal transcribed spacer 2 sequencing, we profiled the gut mycobiome. Five supervised machine learning algorithms were trained on fungal signatures to build an optimized prediction model for LUAD in a discovery cohort comprising 105 patients with LUAD and 61 healthy controls (HCs) from Beijing. Validation cohorts from Beijing, Suzhou, and Hainan comprising 44, 17, and 15 patients with LUAD and 26, 19, and 12 HCs, respectively, were used to evaluate efficacy. RESULTS: Fungal biodiversity and richness increased in patients with LUAD. At the phylum level, the abundance of Ascomycota decreased, while that of Basidiomycota increased in patients with LUAD. Candida and Saccharomyces were the dominant genera, with a reduction in Candida and an increase in Saccharomyces, Aspergillus, and Apiotrichum in patients with LUAD. Nineteen operational taxonomic unit markers were selected, and excellent performance in predicting LUAD was achieved (area under the curve (AUC) = 0.9350) using a random forest model with outcomes superior to those of four other algorithms. The AUCs of the Beijing, Suzhou, and Hainan validation cohorts were 0.9538, 0.9628, and 0.8833, respectively. CONCLUSIONS: For the first time, the gut fungal profiles of patients with LUAD were shown to represent potential non-invasive biomarkers for early-stage diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-023-03095-z. |
format | Online Article Text |
id | pubmed-10617124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106171242023-11-01 Gut mycobiome as a potential non-invasive tool in early detection of lung adenocarcinoma: a cross-sectional study Liu, Qingyan Zhang, Weidong Pei, Yanbin Tao, Haitao Ma, Junxun Li, Rong Zhang, Fan Wang, Lijie Shen, Leilei Liu, Yang Jia, Xiaodong Hu, Yi BMC Med Research Article BACKGROUND: The gut mycobiome of patients with lung adenocarcinoma (LUAD) remains unexplored. This study aimed to characterize the gut mycobiome in patients with LUAD and evaluate the potential of gut fungi as non-invasive biomarkers for early diagnosis. METHODS: In total, 299 fecal samples from Beijing, Suzhou, and Hainan were collected prospectively. Using internal transcribed spacer 2 sequencing, we profiled the gut mycobiome. Five supervised machine learning algorithms were trained on fungal signatures to build an optimized prediction model for LUAD in a discovery cohort comprising 105 patients with LUAD and 61 healthy controls (HCs) from Beijing. Validation cohorts from Beijing, Suzhou, and Hainan comprising 44, 17, and 15 patients with LUAD and 26, 19, and 12 HCs, respectively, were used to evaluate efficacy. RESULTS: Fungal biodiversity and richness increased in patients with LUAD. At the phylum level, the abundance of Ascomycota decreased, while that of Basidiomycota increased in patients with LUAD. Candida and Saccharomyces were the dominant genera, with a reduction in Candida and an increase in Saccharomyces, Aspergillus, and Apiotrichum in patients with LUAD. Nineteen operational taxonomic unit markers were selected, and excellent performance in predicting LUAD was achieved (area under the curve (AUC) = 0.9350) using a random forest model with outcomes superior to those of four other algorithms. The AUCs of the Beijing, Suzhou, and Hainan validation cohorts were 0.9538, 0.9628, and 0.8833, respectively. CONCLUSIONS: For the first time, the gut fungal profiles of patients with LUAD were shown to represent potential non-invasive biomarkers for early-stage diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-023-03095-z. BioMed Central 2023-10-31 /pmc/articles/PMC10617124/ /pubmed/37904139 http://dx.doi.org/10.1186/s12916-023-03095-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Liu, Qingyan Zhang, Weidong Pei, Yanbin Tao, Haitao Ma, Junxun Li, Rong Zhang, Fan Wang, Lijie Shen, Leilei Liu, Yang Jia, Xiaodong Hu, Yi Gut mycobiome as a potential non-invasive tool in early detection of lung adenocarcinoma: a cross-sectional study |
title | Gut mycobiome as a potential non-invasive tool in early detection of lung adenocarcinoma: a cross-sectional study |
title_full | Gut mycobiome as a potential non-invasive tool in early detection of lung adenocarcinoma: a cross-sectional study |
title_fullStr | Gut mycobiome as a potential non-invasive tool in early detection of lung adenocarcinoma: a cross-sectional study |
title_full_unstemmed | Gut mycobiome as a potential non-invasive tool in early detection of lung adenocarcinoma: a cross-sectional study |
title_short | Gut mycobiome as a potential non-invasive tool in early detection of lung adenocarcinoma: a cross-sectional study |
title_sort | gut mycobiome as a potential non-invasive tool in early detection of lung adenocarcinoma: a cross-sectional study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617124/ https://www.ncbi.nlm.nih.gov/pubmed/37904139 http://dx.doi.org/10.1186/s12916-023-03095-z |
work_keys_str_mv | AT liuqingyan gutmycobiomeasapotentialnoninvasivetoolinearlydetectionoflungadenocarcinomaacrosssectionalstudy AT zhangweidong gutmycobiomeasapotentialnoninvasivetoolinearlydetectionoflungadenocarcinomaacrosssectionalstudy AT peiyanbin gutmycobiomeasapotentialnoninvasivetoolinearlydetectionoflungadenocarcinomaacrosssectionalstudy AT taohaitao gutmycobiomeasapotentialnoninvasivetoolinearlydetectionoflungadenocarcinomaacrosssectionalstudy AT majunxun gutmycobiomeasapotentialnoninvasivetoolinearlydetectionoflungadenocarcinomaacrosssectionalstudy AT lirong gutmycobiomeasapotentialnoninvasivetoolinearlydetectionoflungadenocarcinomaacrosssectionalstudy AT zhangfan gutmycobiomeasapotentialnoninvasivetoolinearlydetectionoflungadenocarcinomaacrosssectionalstudy AT wanglijie gutmycobiomeasapotentialnoninvasivetoolinearlydetectionoflungadenocarcinomaacrosssectionalstudy AT shenleilei gutmycobiomeasapotentialnoninvasivetoolinearlydetectionoflungadenocarcinomaacrosssectionalstudy AT liuyang gutmycobiomeasapotentialnoninvasivetoolinearlydetectionoflungadenocarcinomaacrosssectionalstudy AT jiaxiaodong gutmycobiomeasapotentialnoninvasivetoolinearlydetectionoflungadenocarcinomaacrosssectionalstudy AT huyi gutmycobiomeasapotentialnoninvasivetoolinearlydetectionoflungadenocarcinomaacrosssectionalstudy |