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Pan-cancer analyses reveal cancer-type-specific fungal ecologies and bacteriome interactions
Cancer-microbe associations have been explored for centuries, but cancer-associated fungi have rarely been examined. Here, we comprehensively characterize the cancer mycobiome within 17,401 patient tissue, blood, and plasma samples across 35 cancer types in four independent cohorts. We report fungal...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9567272/ https://www.ncbi.nlm.nih.gov/pubmed/36179670 http://dx.doi.org/10.1016/j.cell.2022.09.005 |
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author | Narunsky-Haziza, Lian Sepich-Poore, Gregory D. Livyatan, Ilana Asraf, Omer Martino, Cameron Nejman, Deborah Gavert, Nancy Stajich, Jason E. Amit, Guy González, Antonio Wandro, Stephen Perry, Gili Ariel, Ruthie Meltser, Arnon Shaffer, Justin P. Zhu, Qiyun Balint-Lahat, Nora Barshack, Iris Dadiani, Maya Gal-Yam, Einav N. Patel, Sandip Pravin Bashan, Amir Swafford, Austin D. Pilpel, Yitzhak Knight, Rob Straussman, Ravid |
author_facet | Narunsky-Haziza, Lian Sepich-Poore, Gregory D. Livyatan, Ilana Asraf, Omer Martino, Cameron Nejman, Deborah Gavert, Nancy Stajich, Jason E. Amit, Guy González, Antonio Wandro, Stephen Perry, Gili Ariel, Ruthie Meltser, Arnon Shaffer, Justin P. Zhu, Qiyun Balint-Lahat, Nora Barshack, Iris Dadiani, Maya Gal-Yam, Einav N. Patel, Sandip Pravin Bashan, Amir Swafford, Austin D. Pilpel, Yitzhak Knight, Rob Straussman, Ravid |
author_sort | Narunsky-Haziza, Lian |
collection | PubMed |
description | Cancer-microbe associations have been explored for centuries, but cancer-associated fungi have rarely been examined. Here, we comprehensively characterize the cancer mycobiome within 17,401 patient tissue, blood, and plasma samples across 35 cancer types in four independent cohorts. We report fungal DNA and cells at low abundances across many major human cancers, with differences in community compositions that differ among cancer types, even when accounting for technical background. Fungal histological staining of tissue microarrays supported intratumoral presence and frequent spatial association with cancer cells and macrophages. Comparing intratumoral fungal communities with matched bacteriomes and immunomes revealed co-occurring bi-domain ecologies, often with permissive, rather than competitive, microenvironments and distinct immune responses. Clinically focused assessments suggested prognostic and diagnostic capacities of the tissue and plasma mycobiomes, even in stage I cancers, and synergistic predictive performance with bacteriomes. |
format | Online Article Text |
id | pubmed-9567272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-95672722022-10-16 Pan-cancer analyses reveal cancer-type-specific fungal ecologies and bacteriome interactions Narunsky-Haziza, Lian Sepich-Poore, Gregory D. Livyatan, Ilana Asraf, Omer Martino, Cameron Nejman, Deborah Gavert, Nancy Stajich, Jason E. Amit, Guy González, Antonio Wandro, Stephen Perry, Gili Ariel, Ruthie Meltser, Arnon Shaffer, Justin P. Zhu, Qiyun Balint-Lahat, Nora Barshack, Iris Dadiani, Maya Gal-Yam, Einav N. Patel, Sandip Pravin Bashan, Amir Swafford, Austin D. Pilpel, Yitzhak Knight, Rob Straussman, Ravid Cell Resource Cancer-microbe associations have been explored for centuries, but cancer-associated fungi have rarely been examined. Here, we comprehensively characterize the cancer mycobiome within 17,401 patient tissue, blood, and plasma samples across 35 cancer types in four independent cohorts. We report fungal DNA and cells at low abundances across many major human cancers, with differences in community compositions that differ among cancer types, even when accounting for technical background. Fungal histological staining of tissue microarrays supported intratumoral presence and frequent spatial association with cancer cells and macrophages. Comparing intratumoral fungal communities with matched bacteriomes and immunomes revealed co-occurring bi-domain ecologies, often with permissive, rather than competitive, microenvironments and distinct immune responses. Clinically focused assessments suggested prognostic and diagnostic capacities of the tissue and plasma mycobiomes, even in stage I cancers, and synergistic predictive performance with bacteriomes. Cell Press 2022-09-29 /pmc/articles/PMC9567272/ /pubmed/36179670 http://dx.doi.org/10.1016/j.cell.2022.09.005 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Resource Narunsky-Haziza, Lian Sepich-Poore, Gregory D. Livyatan, Ilana Asraf, Omer Martino, Cameron Nejman, Deborah Gavert, Nancy Stajich, Jason E. Amit, Guy González, Antonio Wandro, Stephen Perry, Gili Ariel, Ruthie Meltser, Arnon Shaffer, Justin P. Zhu, Qiyun Balint-Lahat, Nora Barshack, Iris Dadiani, Maya Gal-Yam, Einav N. Patel, Sandip Pravin Bashan, Amir Swafford, Austin D. Pilpel, Yitzhak Knight, Rob Straussman, Ravid Pan-cancer analyses reveal cancer-type-specific fungal ecologies and bacteriome interactions |
title | Pan-cancer analyses reveal cancer-type-specific fungal ecologies and bacteriome interactions |
title_full | Pan-cancer analyses reveal cancer-type-specific fungal ecologies and bacteriome interactions |
title_fullStr | Pan-cancer analyses reveal cancer-type-specific fungal ecologies and bacteriome interactions |
title_full_unstemmed | Pan-cancer analyses reveal cancer-type-specific fungal ecologies and bacteriome interactions |
title_short | Pan-cancer analyses reveal cancer-type-specific fungal ecologies and bacteriome interactions |
title_sort | pan-cancer analyses reveal cancer-type-specific fungal ecologies and bacteriome interactions |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9567272/ https://www.ncbi.nlm.nih.gov/pubmed/36179670 http://dx.doi.org/10.1016/j.cell.2022.09.005 |
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