Cargando…

Oral mycobiota and pancreatic ductal adenocarcinoma

Early detection of pancreatic ductal adenocarcinoma (PDAC) is essential for survival. Preliminary research demonstrated significant associations between structural alternation of mycobiota and PDAC. In this study, we investigated the associations between oral mycobiota and PDAC. We further explored...

Descripción completa

Detalles Bibliográficos
Autores principales: Wei, Ailin, Zhao, Huiling, Cong, Xue, Wang, Linyao, Chen, Yiyang, Gou, Juxiang, Hu, Ziyi, Hu, Xiuying, Tian, Yali, Li, Ka, Deng, Yufeng, Zuo, Haojiang, Fu, Mei Rosemary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9716801/
https://www.ncbi.nlm.nih.gov/pubmed/36460974
http://dx.doi.org/10.1186/s12885-022-10329-5
_version_ 1784842770243911680
author Wei, Ailin
Zhao, Huiling
Cong, Xue
Wang, Linyao
Chen, Yiyang
Gou, Juxiang
Hu, Ziyi
Hu, Xiuying
Tian, Yali
Li, Ka
Deng, Yufeng
Zuo, Haojiang
Fu, Mei Rosemary
author_facet Wei, Ailin
Zhao, Huiling
Cong, Xue
Wang, Linyao
Chen, Yiyang
Gou, Juxiang
Hu, Ziyi
Hu, Xiuying
Tian, Yali
Li, Ka
Deng, Yufeng
Zuo, Haojiang
Fu, Mei Rosemary
author_sort Wei, Ailin
collection PubMed
description Early detection of pancreatic ductal adenocarcinoma (PDAC) is essential for survival. Preliminary research demonstrated significant associations between structural alternation of mycobiota and PDAC. In this study, we investigated the associations between oral mycobiota and PDAC. We further explored mycobiota biomarkers for PDAC detection. We enrolled 34 PDAC patients and 35 matched healthy controls from West China hospital in Southwest China. Demographic data, clinical information, and salivary samples were collected. Mycobiota characteristics were defined using Internal Transcribed Spacer (ITS) ribosomal RNA sequencing. We found that the PDAC patients had significant increase in fungal abundance (P < 0.001) and significant decrease in fungal diversity (P < 0.001) in comparison to the healthy controls. A higher abundance of Basidiomycota and Unclassifed_p_Ascomycota was associated with an increased risk of PDAC. With each increase of abundance of g__unclassified_k__Fungi and g__unclassified_p__Ascomycota in PDAC patients, the risk of pancreatic cancer increased by 1.359 odds and 1.260 odds, respectively. Aspergillus (AUC = 0.983, 95% CI 0.951–1.000) and Cladosporium (AUC = 0.969, 95% CI 0.921–1.000) achieved high classification powers to distinguish PDAC patients from the healthy controls. The rapid, inexpensive tests of ITS1 sequencing of mycobiota and PCR detection of potential fungal biomarkers make it promising for the clinical practice to use oral microbes for PDAC early detection and prevention. Results of our study provide evidence that salivary mycobiota may provide insights into cancer risk, prevention, and detection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10329-5.
format Online
Article
Text
id pubmed-9716801
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-97168012022-12-03 Oral mycobiota and pancreatic ductal adenocarcinoma Wei, Ailin Zhao, Huiling Cong, Xue Wang, Linyao Chen, Yiyang Gou, Juxiang Hu, Ziyi Hu, Xiuying Tian, Yali Li, Ka Deng, Yufeng Zuo, Haojiang Fu, Mei Rosemary BMC Cancer Research Early detection of pancreatic ductal adenocarcinoma (PDAC) is essential for survival. Preliminary research demonstrated significant associations between structural alternation of mycobiota and PDAC. In this study, we investigated the associations between oral mycobiota and PDAC. We further explored mycobiota biomarkers for PDAC detection. We enrolled 34 PDAC patients and 35 matched healthy controls from West China hospital in Southwest China. Demographic data, clinical information, and salivary samples were collected. Mycobiota characteristics were defined using Internal Transcribed Spacer (ITS) ribosomal RNA sequencing. We found that the PDAC patients had significant increase in fungal abundance (P < 0.001) and significant decrease in fungal diversity (P < 0.001) in comparison to the healthy controls. A higher abundance of Basidiomycota and Unclassifed_p_Ascomycota was associated with an increased risk of PDAC. With each increase of abundance of g__unclassified_k__Fungi and g__unclassified_p__Ascomycota in PDAC patients, the risk of pancreatic cancer increased by 1.359 odds and 1.260 odds, respectively. Aspergillus (AUC = 0.983, 95% CI 0.951–1.000) and Cladosporium (AUC = 0.969, 95% CI 0.921–1.000) achieved high classification powers to distinguish PDAC patients from the healthy controls. The rapid, inexpensive tests of ITS1 sequencing of mycobiota and PCR detection of potential fungal biomarkers make it promising for the clinical practice to use oral microbes for PDAC early detection and prevention. Results of our study provide evidence that salivary mycobiota may provide insights into cancer risk, prevention, and detection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10329-5. BioMed Central 2022-12-02 /pmc/articles/PMC9716801/ /pubmed/36460974 http://dx.doi.org/10.1186/s12885-022-10329-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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
Wei, Ailin
Zhao, Huiling
Cong, Xue
Wang, Linyao
Chen, Yiyang
Gou, Juxiang
Hu, Ziyi
Hu, Xiuying
Tian, Yali
Li, Ka
Deng, Yufeng
Zuo, Haojiang
Fu, Mei Rosemary
Oral mycobiota and pancreatic ductal adenocarcinoma
title Oral mycobiota and pancreatic ductal adenocarcinoma
title_full Oral mycobiota and pancreatic ductal adenocarcinoma
title_fullStr Oral mycobiota and pancreatic ductal adenocarcinoma
title_full_unstemmed Oral mycobiota and pancreatic ductal adenocarcinoma
title_short Oral mycobiota and pancreatic ductal adenocarcinoma
title_sort oral mycobiota and pancreatic ductal adenocarcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9716801/
https://www.ncbi.nlm.nih.gov/pubmed/36460974
http://dx.doi.org/10.1186/s12885-022-10329-5
work_keys_str_mv AT weiailin oralmycobiotaandpancreaticductaladenocarcinoma
AT zhaohuiling oralmycobiotaandpancreaticductaladenocarcinoma
AT congxue oralmycobiotaandpancreaticductaladenocarcinoma
AT wanglinyao oralmycobiotaandpancreaticductaladenocarcinoma
AT chenyiyang oralmycobiotaandpancreaticductaladenocarcinoma
AT goujuxiang oralmycobiotaandpancreaticductaladenocarcinoma
AT huziyi oralmycobiotaandpancreaticductaladenocarcinoma
AT huxiuying oralmycobiotaandpancreaticductaladenocarcinoma
AT tianyali oralmycobiotaandpancreaticductaladenocarcinoma
AT lika oralmycobiotaandpancreaticductaladenocarcinoma
AT dengyufeng oralmycobiotaandpancreaticductaladenocarcinoma
AT zuohaojiang oralmycobiotaandpancreaticductaladenocarcinoma
AT fumeirosemary oralmycobiotaandpancreaticductaladenocarcinoma