TY - JOUR
T1 - Distinct microbial signatures associated with different breast cancer types
AU - Banerjee, Sagarika
AU - Tian, Tian
AU - Wei, Zhi
AU - Shih, Natalie
AU - Feldman, Michael D.
AU - Peck, Kristen N.
AU - DeMichele, Angela M.
AU - Alwine, James C.
AU - Robertson, Erle S.
N1 - Publisher Copyright:
© 2018 Banerjee, Tian, Wei, Shih, Feldman, Peck, DeMichele, Alwine and Robertson.
PY - 2018/5/15
Y1 - 2018/5/15
N2 - A dysbiotic microbiome can potentially contribute to the pathogenesis of many different diseases including cancer. Breast cancer is the second leading cause of cancer death in women. Thus, we investigated the diversity of the microbiome in the four major types of breast cancer: endocrine receptor (ER) positive, triple positive, Her2 positive and triple negative breast cancers. Using a whole genome and transcriptome amplification and a pan-pathogen microarray (PathoChip) strategy, we detected unique and common viral, bacterial, fungal and parasitic signatures for each of the breast cancer types. These were validated by PCR and Sanger sequencing. Hierarchical cluster analysis of the breast cancer samples, based on their detected microbial signatures, showed distinct patterns for the triple negative and triple positive samples, while the ER positive and Her2 positive samples shared similar microbial signatures. These signatures, unique or common to the different breast cancer types, provide a new line of investigation to gain further insights into prognosis, treatment strategies and clinical outcome, as well as better understanding of the role of the micro-organisms in the development and progression of breast cancer.
AB - A dysbiotic microbiome can potentially contribute to the pathogenesis of many different diseases including cancer. Breast cancer is the second leading cause of cancer death in women. Thus, we investigated the diversity of the microbiome in the four major types of breast cancer: endocrine receptor (ER) positive, triple positive, Her2 positive and triple negative breast cancers. Using a whole genome and transcriptome amplification and a pan-pathogen microarray (PathoChip) strategy, we detected unique and common viral, bacterial, fungal and parasitic signatures for each of the breast cancer types. These were validated by PCR and Sanger sequencing. Hierarchical cluster analysis of the breast cancer samples, based on their detected microbial signatures, showed distinct patterns for the triple negative and triple positive samples, while the ER positive and Her2 positive samples shared similar microbial signatures. These signatures, unique or common to the different breast cancer types, provide a new line of investigation to gain further insights into prognosis, treatment strategies and clinical outcome, as well as better understanding of the role of the micro-organisms in the development and progression of breast cancer.
KW - Endocrine receptor positive breast cancer
KW - HER2 positive breast cancer
KW - Microbiome
KW - Triple negative breast cancer
KW - Triple positive breast cancer
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U2 - 10.3389/fmicb.2018.00951
DO - 10.3389/fmicb.2018.00951
M3 - Article
AN - SCOPUS:85047019651
SN - 1664-302X
VL - 9
JO - Frontiers in Microbiology
JF - Frontiers in Microbiology
IS - MAY
M1 - 951
ER -