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High-throughput nucleotide sequencing for bacteriome studies in oral squamous cell carcinoma: a systematic review

Journal

ORAL AND MAXILLOFACIAL SURGERY-HEIDELBERG
Volume 24, Issue 4, Pages 387-401

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s10006-020-00873-4

Keywords

Oral squamous cell carcinoma; Microbiota; Metagenomics; High-throughput nucleotide sequencing; 16S

Funding

  1. National Council for Scientific and Technological Development (CNPq) [211309/2013-3]
  2. Foundation for Research Financial Support in the State of Rio de Janeiro (FAPERJ), Rio de Janeiro, Brazil [E26/103.001/2012]

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Purpose Dysbiosis has been identified in oral squamous cell carcinoma (OSCC). The aim of this study was to carry out a systematic review of an electronic research that was carried out on articles published between January 2008 and September 2018. Methods Eight studies were selected after applying the inclusion and exclusion criteria. Results All articles targeted the hypervariable regions of the 16S rRNA gene. At the phylum level, it was found reduction of Bacteroidetes (2/8 studies) and increase of Firmicutes (2/8 studies). At the genus level, Rothia increased (1/8 studies) and decreased (2/8 studies) in tumor samples, and Streptococcus also was found increased (3/8 studies) and reduced (3/8 studies). Fusobacterium only increased in OSCC samples (3/8 studies). At species level, an increase in F. nucleatum subsp. polymorphum was more associated to OSCC (2/8 studies) than with controls, as was P. aeruginosa (3/8 studies). Conclusion In summary, the results corroborated dysbiosis in OSCC patients, with enrichment of microbial taxa that are associated with inflammation and production of acetaldehyde. However, variations of study design and sample size were observed among the studies, as well as a shortage of more detailed analyses of possible correlations between risk habits and OSCC. This lack of more detailed analysis may be the cause of the inconsistencies in regard of the alterations reported for certain genera and species. In conclusion, there is an association between OSCC and oral microbiota dysbiosis, but its role in oral carcinogenesis needs to be clarified in more detail.

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