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Prognostic correlations with the microbiome of breast cancer subtypes.
Banerjee, Sagarika; Wei, Zhi; Tian, Tian; Bose, Dipayan; Shih, Natalie N C; Feldman, Michael D; Khoury, Thaer; De Michele, Angela; Robertson, Erle S.
Afiliación
  • Banerjee S; Department of Otorhinolaryngology-Head and Neck Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Wei Z; Department of Computer Science, New Jersey Institute of Technology, Newark, NJ, USA.
  • Tian T; Department of Computer Science, New Jersey Institute of Technology, Newark, NJ, USA.
  • Bose D; Department of Otorhinolaryngology-Head and Neck Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Shih NNC; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Feldman MD; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Khoury T; Department of Pathology, Roswell Park Cancer Institute, Buffalo, NY, USA.
  • De Michele A; Division of Hematology Oncology, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Robertson ES; Department of Otorhinolaryngology-Head and Neck Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. erle@pennmedicine.upenn.edu.
Cell Death Dis ; 12(9): 831, 2021 09 04.
Article en En | MEDLINE | ID: mdl-34482363
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Microbiota Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: Cell Death Dis Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Microbiota Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: Cell Death Dis Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos