TY - JOUR
T1 - Pan-cancer analyses reveal cancer-type-specific fungal ecologies and bacteriome interactions
AU - Narunsky-Haziza, Lian
AU - Sepich-Poore, Gregory D.
AU - Livyatan, Ilana
AU - Asraf, Omer
AU - Martino, Cameron
AU - Nejman, Deborah
AU - Gavert, Nancy
AU - Stajich, Jason E.
AU - Amit, Guy
AU - González, Antonio
AU - Wandro, Stephen
AU - Perry, Gili
AU - Ariel, Ruthie
AU - Meltser, Arnon
AU - Shaffer, Justin P.
AU - Zhu, Qiyun
AU - Balint-Lahat, Nora
AU - Barshack, Iris
AU - Dadiani, Maya
AU - Gal-Yam, Einav N.
AU - Patel, Sandip Pravin
AU - Bashan, Amir
AU - Swafford, Austin D.
AU - Pilpel, Yitzhak
AU - Knight, Rob
AU - Straussman, Ravid
N1 - Publisher Copyright: © 2022 The Authors
PY - 2022/9/29
Y1 - 2022/9/29
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85138486612&partnerID=8YFLogxK
U2 - 10.1016/j.cell.2022.09.005
DO - 10.1016/j.cell.2022.09.005
M3 - مقالة
C2 - 36179670
SN - 0092-8674
VL - 185
SP - 3789
EP - 3806
JO - Cell
JF - Cell
IS - 20
ER -