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Distribution of microbiota in cervical preneoplasia of racially disparate populations.
Vikramdeo, Kunwar Somesh; Anand, Shashi; Pierce, Jennifer Young; Singh, Ajay Pratap; Singh, Seema; Dasgupta, Santanu.
Affiliation
  • Vikramdeo KS; Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
  • Anand S; Department of Pathology, College of Medicine, Mitchell Cancer Institute, University of South Alabama, 1660 Springhill Avenue, Mobile, AL, 36604, USA.
  • Pierce JY; Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
  • Singh AP; Department of Pathology, College of Medicine, Mitchell Cancer Institute, University of South Alabama, 1660 Springhill Avenue, Mobile, AL, 36604, USA.
  • Singh S; Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
  • Dasgupta S; Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
BMC Cancer ; 22(1): 1074, 2022 Oct 18.
Article in En | MEDLINE | ID: mdl-36258167
ABSTRACT
BACKGROUNDS Microbiome dysbiosis is an important contributing factor in tumor development and thus may be a risk predictor for human malignancies. In the United States, women with Hispanic/Latina (HIS) and African American (AA) background have a higher incidence of cervical cancer and poorer outcomes than Caucasian American (CA) women.

METHODS:

Here, we assessed the distribution pattern of microbiota in cervical intraepithelial neoplasia (CIN) lesions obtained from HIS (n = 12), AA (n = 12), and CA (n = 12) women, who were screened for CC risk assessment. We employed a 16S rRNA gene sequencing approach adapted from the NIH-Human Microbiome Project to identify the microbial niche in all CIN lesions (n = 36).

RESULTS:

We detected an appreciably decreased abundance of beneficial Lactobacillus in the CIN lesions of the AA and HIS women compared to the CA women. Differential abundance of potentially pathogenic Prevotella, Delftia, Gardnerella, and Fastidiosipila was also evident among the various racial groups. An increased abundance of Micrococcus was also evident in AA and HIS women compared to the CA women. The detection level of Rhizobium was higher among the AA ad CA women compared to the HIS women. In addition to the top 10 microbes, a unique niche of 27 microbes was identified exclusively in women with a histopathological diagnosis of CIN. Among these microbes, a group of 8 microbiota; Rubellimicrobium, Podobacter, Brevibacterium, Paracoccus, Atopobium, Brevundimonous, Comamonous, and Novospingobium was detected only in the CIN lesions obtained from AA and CA women.

CONCLUSIONS:

Microbial dysbiosis in the cervical epithelium represented by an increased ratio of potentially pathogenic to beneficial microbes may be associated with increased CC risk disparities. Developing a race-specific reliable panel of microbial markers could be beneficial for CC risk assessment, disease prevention, and/or therapeutic guidance.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Uterine Cervical Dysplasia / Uterine Cervical Neoplasms / Papillomavirus Infections / Microbiota Type of study: Guideline / Prognostic_studies / Risk_factors_studies Limits: Female / Humans Language: En Journal: BMC Cancer Journal subject: NEOPLASIAS Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Uterine Cervical Dysplasia / Uterine Cervical Neoplasms / Papillomavirus Infections / Microbiota Type of study: Guideline / Prognostic_studies / Risk_factors_studies Limits: Female / Humans Language: En Journal: BMC Cancer Journal subject: NEOPLASIAS Year: 2022 Document type: Article Affiliation country:
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