Your browser doesn't support javascript.
loading
The intratumor mycobiome promotes lung cancer progression via myeloid-derived suppressor cells.
Liu, Ning-Ning; Yi, Cheng-Xiang; Wei, Lu-Qi; Zhou, Jin-An; Jiang, Tong; Hu, Cong-Cong; Wang, Lu; Wang, Yuan-Yuan; Zou, Yun; Zhao, Yi-Kai; Zhang, Le-Le; Nie, Ya-Ting; Zhu, Yi-Jing; Yi, Xin-Yao; Zeng, Ling-Bing; Li, Jing-Quan; Huang, Xiao-Tian; Ji, Hong-Bin; Kozlakidis, Zisis; Zhong, Lin; Heeschen, Christopher; Zheng, Xiao-Qi; Chen, Changbin; Zhang, Peng; Wang, Hui.
Affiliation
  • Liu NN; State Key Laboratory of Systems Medicine for Cancer, Center for Single-Cell Omics, School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China. Electronic address: liuningning@shsmu.edu.cn.
  • Yi CX; Department of Thoracic Surgery, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai 200433, China; Central Laboratory, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai 200433, China.
  • Wei LQ; State Key Laboratory of Systems Medicine for Cancer, Center for Single-Cell Omics, School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
  • Zhou JA; State Key Laboratory of Systems Medicine for Cancer, Center for Single-Cell Omics, School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
  • Jiang T; Shanghai Institute of Immunity and Infection, Chinese Academy of Science, (Past Name: Institut Pasteur of Shanghai, Chinese Academy of Sciences), Shanghai 200031, China; Laboratory Services and Biobanking, International Agency for Research on Cancer, World Health Organization, Lyon, France.
  • Hu CC; Department of Mathematics, Shanghai Normal University, Shanghai 200234, China.
  • Wang L; Department of Mathematics, Shanghai Normal University, Shanghai 200234, China.
  • Wang YY; Shanghai Institute of Immunity and Infection, Chinese Academy of Science, (Past Name: Institut Pasteur of Shanghai, Chinese Academy of Sciences), Shanghai 200031, China.
  • Zou Y; Shanghai Institute of Immunity and Infection, Chinese Academy of Science, (Past Name: Institut Pasteur of Shanghai, Chinese Academy of Sciences), Shanghai 200031, China.
  • Zhao YK; State Key Laboratory of Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
  • Zhang LL; Department of Thoracic Surgery, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai 200433, China; Central Laboratory, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai 200433, China.
  • Nie YT; Department of Mathematics, Shanghai Normal University, Shanghai 200234, China.
  • Zhu YJ; Department of Mathematics, Shanghai Normal University, Shanghai 200234, China.
  • Yi XY; Department of Mathematics, Shanghai Normal University, Shanghai 200234, China.
  • Zeng LB; Department of Laboratory Medicine, The First Affiliated Hospital of Nanchang University, Nanchang 330052, China.
  • Li JQ; State Key Laboratory of Systems Medicine for Cancer, Center for Single-Cell Omics, School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
  • Huang XT; Department of Medical Microbiology, School of Medicine, Nanchang University, Nanchang 330052, China.
  • Ji HB; State Key Laboratory of Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
  • Kozlakidis Z; Laboratory Services and Biobanking, International Agency for Research on Cancer, World Health Organization, Lyon, France.
  • Zhong L; Department of General Surgery, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200080, China.
  • Heeschen C; State Key Laboratory of Systems Medicine for Cancer, Center for Single-Cell Omics, School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
  • Zheng XQ; State Key Laboratory of Systems Medicine for Cancer, Center for Single-Cell Omics, School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
  • Chen C; Shanghai Institute of Immunity and Infection, Chinese Academy of Science, (Past Name: Institut Pasteur of Shanghai, Chinese Academy of Sciences), Shanghai 200031, China; Nanjing Advanced Academy of Life and Health, Nanjing 211135, China. Electronic address: cbchen@ips.ac.cn.
  • Zhang P; Department of Thoracic Surgery, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai 200433, China. Electronic address: zhangpeng1121@tongji.edu.cn.
  • Wang H; State Key Laboratory of Systems Medicine for Cancer, Center for Single-Cell Omics, School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China. Electronic address: huiwang@shsmu.edu.cn.
Cancer Cell ; 41(11): 1927-1944.e9, 2023 11 13.
Article in En | MEDLINE | ID: mdl-37738973
ABSTRACT
Although polymorphic microbiomes have emerged as hallmarks of cancer, far less is known about the role of the intratumor mycobiome as living microorganisms in cancer progression. Here, using fungi-enriched DNA extraction and deep shotgun metagenomic sequencing, we have identified enriched tumor-resident Aspergillus sydowii in patients with lung adenocarcinoma (LUAD). By three different syngeneic lung cancer mice models, we find that A. sydowii promotes lung tumor progression via IL-1ß-mediated expansion and activation of MDSCs, resulting in suppressed activity of cytotoxic T lymphocyte cells and accumulation of PD-1+ CD8+ T cells. This is mediated by IL-1ß secretion via ß-glucan/Dectin-1/CARD9 pathway. Analysis of human samples confirms that enriched A. sydowii is associated with immunosuppression and poor patient outcome. Our findings suggest that intratumor mycobiome, albeit at low biomass, promotes lung cancer progression and could be targeted at the strain level to improve patients with LUAD outcome.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myeloid-Derived Suppressor Cells / Mycobiome / Lung Neoplasms Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Cancer Cell Journal subject: NEOPLASIAS Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Myeloid-Derived Suppressor Cells / Mycobiome / Lung Neoplasms Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: Cancer Cell Journal subject: NEOPLASIAS Year: 2023 Document type: Article