Metatranscriptomic Analysis of Human Lung Metagenomes from Patients with Lung Cancer
This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed....
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Published in | Genes Vol. 12; no. 9; p. 1458 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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21.09.2021
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ISSN | 2073-4425 2073-4425 |
DOI | 10.3390/genes12091458 |
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Abstract | This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed. The heterogeneous cellular landscape and immune repertoires of the lung samples were examined using xCell and TRUST4, respectively. We found that nine bacteria were significantly enriched in the lung tissues of cancer patients, and associated with reduced overall survival (OS). We also found that subjects with mutations in the epidermal growth factor receptor gene were less likely to experience the presence of Pseudomonas. aeruginosa. We found that the presence of CD8+ T-cells, CD4+ naive T-cells, dendritic cells, and CD4+ central memory T cells were associated with a good prognosis, while the presence of pro B-cells was associated with a poor prognosis. Furthermore, high clone numbers were associated with a high ImmuneScore for all immune receptor repertoires. Clone numbers and diversity were significantly higher in unpresented subjects compared to presented subjects. Our results provide insight into the microbiota of human lung cancer, and how its composition is linked to the tumor immune microenvironment, immune receptor repertoires, and OS. |
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AbstractList | This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed. The heterogeneous cellular landscape and immune repertoires of the lung samples were examined using xCell and TRUST4, respectively. We found that nine bacteria were significantly enriched in the lung tissues of cancer patients, and associated with reduced overall survival (OS). We also found that subjects with mutations in the epidermal growth factor receptor gene were less likely to experience the presence of Pseudomonas. aeruginosa. We found that the presence of CD8+ T-cells, CD4+ naive T-cells, dendritic cells, and CD4+ central memory T cells were associated with a good prognosis, while the presence of pro B-cells was associated with a poor prognosis. Furthermore, high clone numbers were associated with a high ImmuneScore for all immune receptor repertoires. Clone numbers and diversity were significantly higher in unpresented subjects compared to presented subjects. Our results provide insight into the microbiota of human lung cancer, and how its composition is linked to the tumor immune microenvironment, immune receptor repertoires, and OS. This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed. The heterogeneous cellular landscape and immune repertoires of the lung samples were examined using xCell and TRUST4, respectively. We found that nine bacteria were significantly enriched in the lung tissues of cancer patients, and associated with reduced overall survival (OS). We also found that subjects with mutations in the epidermal growth factor receptor gene were less likely to experience the presence of . We found that the presence of CD8+ T-cells, CD4+ naive T-cells, dendritic cells, and CD4+ central memory T cells were associated with a good prognosis, while the presence of pro B-cells was associated with a poor prognosis. Furthermore, high clone numbers were associated with a high ImmuneScore for all immune receptor repertoires. Clone numbers and diversity were significantly higher in unpresented subjects compared to presented subjects. Our results provide insight into the microbiota of human lung cancer, and how its composition is linked to the tumor immune microenvironment, immune receptor repertoires, and OS. This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed. The heterogeneous cellular landscape and immune repertoires of the lung samples were examined using xCell and TRUST4, respectively. We found that nine bacteria were significantly enriched in the lung tissues of cancer patients, and associated with reduced overall survival (OS). We also found that subjects with mutations in the epidermal growth factor receptor gene were less likely to experience the presence of Pseudomonas. aeruginosa . We found that the presence of CD8+ T-cells, CD4+ naive T-cells, dendritic cells, and CD4+ central memory T cells were associated with a good prognosis, while the presence of pro B-cells was associated with a poor prognosis. Furthermore, high clone numbers were associated with a high ImmuneScore for all immune receptor repertoires. Clone numbers and diversity were significantly higher in unpresented subjects compared to presented subjects. Our results provide insight into the microbiota of human lung cancer, and how its composition is linked to the tumor immune microenvironment, immune receptor repertoires, and OS. This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed. The heterogeneous cellular landscape and immune repertoires of the lung samples were examined using xCell and TRUST4, respectively. We found that nine bacteria were significantly enriched in the lung tissues of cancer patients, and associated with reduced overall survival (OS). We also found that subjects with mutations in the epidermal growth factor receptor gene were less likely to experience the presence of Pseudomonas. aeruginosa. We found that the presence of CD8+ T-cells, CD4+ naive T-cells, dendritic cells, and CD4+ central memory T cells were associated with a good prognosis, while the presence of pro B-cells was associated with a poor prognosis. Furthermore, high clone numbers were associated with a high ImmuneScore for all immune receptor repertoires. Clone numbers and diversity were significantly higher in unpresented subjects compared to presented subjects. Our results provide insight into the microbiota of human lung cancer, and how its composition is linked to the tumor immune microenvironment, immune receptor repertoires, and OS.This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49 patients with lung cancer. Metatranscriptomics data were analyzed using SAMSA2 and Kraken2 software. 16S rRNA sequencing was also performed. The heterogeneous cellular landscape and immune repertoires of the lung samples were examined using xCell and TRUST4, respectively. We found that nine bacteria were significantly enriched in the lung tissues of cancer patients, and associated with reduced overall survival (OS). We also found that subjects with mutations in the epidermal growth factor receptor gene were less likely to experience the presence of Pseudomonas. aeruginosa. We found that the presence of CD8+ T-cells, CD4+ naive T-cells, dendritic cells, and CD4+ central memory T cells were associated with a good prognosis, while the presence of pro B-cells was associated with a poor prognosis. Furthermore, high clone numbers were associated with a high ImmuneScore for all immune receptor repertoires. Clone numbers and diversity were significantly higher in unpresented subjects compared to presented subjects. Our results provide insight into the microbiota of human lung cancer, and how its composition is linked to the tumor immune microenvironment, immune receptor repertoires, and OS. |
Author | Fang, Hsin-Yuan Hsu, Ming-Hung Yen, Ju-Chen Chang, Ya-Sian Tu, Siang-Jyun Lee, Ya-Ting Chang, Jan-Gowth |
AuthorAffiliation | 5 Department of Bioinformatics and Medical Engineering, Asia University, Taichung 413, Taiwan 1 Epigenome Research Center, China Medical University Hospital, Taichung 404, Taiwan; t25074@mail.cmuh.org.tw (Y.-S.C.); t24399@mail.cmuh.org.tw (J.-C.Y.); t23701@mail.cmuh.org.tw (Y.-T.L.) 2 Center for Precision Medicine, China Medical University Hospital, Taichung 404, Taiwan; t35492@mail.cmuh.org.tw (M.-H.H.); t34752@mail.cmuh.org.tw (S.-J.T.) 4 Department of Thoracic Surgery, China Medical University Hospital, Taichung 404, Taiwan; d17573@mail.cmuh.org.tw 3 School of Medicine, China Medical University, Taichung 404, Taiwan |
AuthorAffiliation_xml | – name: 3 School of Medicine, China Medical University, Taichung 404, Taiwan – name: 4 Department of Thoracic Surgery, China Medical University Hospital, Taichung 404, Taiwan; d17573@mail.cmuh.org.tw – name: 1 Epigenome Research Center, China Medical University Hospital, Taichung 404, Taiwan; t25074@mail.cmuh.org.tw (Y.-S.C.); t24399@mail.cmuh.org.tw (J.-C.Y.); t23701@mail.cmuh.org.tw (Y.-T.L.) – name: 2 Center for Precision Medicine, China Medical University Hospital, Taichung 404, Taiwan; t35492@mail.cmuh.org.tw (M.-H.H.); t34752@mail.cmuh.org.tw (S.-J.T.) – name: 5 Department of Bioinformatics and Medical Engineering, Asia University, Taichung 413, Taiwan |
Author_xml | – sequence: 1 givenname: Ya-Sian surname: Chang fullname: Chang, Ya-Sian – sequence: 2 givenname: Ming-Hung surname: Hsu fullname: Hsu, Ming-Hung – sequence: 3 givenname: Siang-Jyun orcidid: 0000-0002-6385-8683 surname: Tu fullname: Tu, Siang-Jyun – sequence: 4 givenname: Ju-Chen surname: Yen fullname: Yen, Ju-Chen – sequence: 5 givenname: Ya-Ting surname: Lee fullname: Lee, Ya-Ting – sequence: 6 givenname: Hsin-Yuan surname: Fang fullname: Fang, Hsin-Yuan – sequence: 7 givenname: Jan-Gowth orcidid: 0000-0003-0375-1427 surname: Chang fullname: Chang, Jan-Gowth |
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Keywords | lung cancer T cell receptor repertoires metatranscriptomic B cell receptor repertoires microenvironments |
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Snippet | This study was designed to characterize the microbiomes of the lung tissues of lung cancer patients. RNA-sequencing was performed on lung tumor samples from 49... |
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SubjectTerms | Adenocarcinoma of Lung - genetics Adenocarcinoma of Lung - immunology Adenocarcinoma of Lung - microbiology Bacterial infections Carcinoma, Non-Small-Cell Lung - genetics Carcinoma, Non-Small-Cell Lung - immunology Carcinoma, Non-Small-Cell Lung - microbiology Carcinoma, Non-Small-Cell Lung - mortality Carcinoma, Squamous Cell - genetics Carcinoma, Squamous Cell - immunology Carcinoma, Squamous Cell - microbiology CD4 antigen CD8 antigen CD8-positive T-lymphocytes computer software Dendritic cells Disease Epidermal growth factor epidermal growth factor receptors Gene Expression Profiling genes Genomes Humans immunologic receptors Immunological memory landscapes Lavage Lung cancer lung neoplasms Lung Neoplasms - genetics Lung Neoplasms - immunology Lung Neoplasms - microbiology Lung Neoplasms - mortality lungs Lymphocytes B Lymphocytes T Medical prognosis memory Memory cells Metagenome metagenomics microbiome Microbiomes Microbiota Microenvironments Microorganisms Mutation Pilot Projects Prognosis Pseudomonas Receptors, Antigen, B-Cell - immunology Receptors, Antigen, T-Cell - immunology RNA, Ribosomal, 16S rRNA 16S sequence analysis Sequence Analysis, RNA Software Survival analysis T cell receptors Taxonomy transcriptomics Tumor Microenvironment - immunology Tumors |
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Title | Metatranscriptomic Analysis of Human Lung Metagenomes from Patients with Lung Cancer |
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