Prognostic correlations with the microbiome of breast cancer subtypes

被引:71
作者
Banerjee, Sagarika [1 ]
Wei, Zhi [2 ]
Tian, Tian [2 ]
Bose, Dipayan [1 ]
Shih, Natalie N. C. [3 ]
Feldman, Michael D. [3 ]
Khoury, Thaer [4 ]
De Michele, Angela [5 ]
Robertson, Erle S. [1 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Philadelphia, PA 19104 USA
[2] New Jersey Inst Technol, Dept Comp Sci, Newark, NJ 07102 USA
[3] Univ Penn, Perelman Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[4] Roswell Park Canc Inst, Dept Pathol, Buffalo, NY USA
[5] Univ Penn, Perelman Sch Med, Dept Med, Div Hematol Oncol, Philadelphia, PA 19104 USA
关键词
ENDOTHELIAL GROWTH-FACTOR; GUT MICROBIOME; CARCINOMA; SEQUENCE;
D O I
10.1038/s41419-021-04092-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Alterations to the natural microbiome are linked to different diseases, and the presence or absence of specific microbes is directly related to disease outcomes. We performed a comprehensive analysis with unique cohorts of the four subtypes of breast cancer (BC) characterized by their microbial signatures, using a pan-pathogen microarray strategy. The signature (includes viruses, bacteria, fungi, and parasites) of each tumor subtype was correlated with clinical data to identify microbes with prognostic potential. The subtypes of BC had specific viromes and microbiomes, with ER+ and TN tumors showing the most and least diverse microbiome, respectively. The specific microbial signatures allowed discrimination between different BC subtypes. Furthermore, we demonstrated correlations between the presence and absence of specific microbes in BC subtypes with the clinical outcomes. This study provides a comprehensive map of the oncobiome of BC subtypes, with insights into disease prognosis that can be critical for precision therapeutic intervention strategies.
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页数:14
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