完整後設資料紀錄
DC 欄位語言
dc.contributor.authorYang, Shun-Faen_US
dc.contributor.authorHuang, Hsien-Daen_US
dc.contributor.authorFan, Wen-Langen_US
dc.contributor.authorJong, Yuh-Jyhen_US
dc.contributor.authorChen, Mu-Kuanen_US
dc.contributor.authorHuang, Chien-Ningen_US
dc.contributor.authorChuang, Chun-Yien_US
dc.contributor.authorKuo, Yu-Lunen_US
dc.contributor.authorChung, Wen-Hungen_US
dc.contributor.authorSu, Shih-Chien_US
dc.date.accessioned2018-08-21T05:53:18Z-
dc.date.available2018-08-21T05:53:18Z-
dc.date.issued2018-02-01en_US
dc.identifier.issn1368-8375en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.oraloncology.2017.12.005en_US
dc.identifier.urihttp://hdl.handle.net/11536/144507-
dc.description.abstractObjectives: Both genetic and environmental factors are conceivably required to assess the prognosis of oral squamous cell carcinoma (OSCC), yet little is known regarding the relationship between oral microbiome and the mutational spectrum of OSCC. Materials and methods: Here, we used 16S rRNA amplicon sequencing to study the composition of oral microorganisms in OSCC patients, whose cancer mutational profiles were previously defined by whole-exome sequencing, to evaluate the relationship between oral microbiome and the mutational changes in OSCC. Results: Analyzing the contributions of the five mutational signatures extracted from the primary tumors revealed three groups of OSCC (mutational signature cluster, MSC1-3) that were significantly associated with demographic and clinical features. Taxonomic analysis of the predominant phyla in salivary samples showed variation in the relative abundance of Firmicutes and Bacteroidetes in the three MSC groups. In addition, significant differences in bacterial species richness (alpha diversity) and slight sample-to-sample dissimilarities in bacterial community structures (beta diversity) were noted among different MSC groups. Further, predicting the functional capabilities of microbial communities by reconstruction of unobserved states showed that many pathways related to cell motility were differentially enriched among the three MSC groups. Conclusion: Collectively, these results indicate a potential association of oral microbiome with the mutational changes in OSCC.en_US
dc.language.isoen_USen_US
dc.subjectOral squamous cell carcinomaen_US
dc.subjectOral microbiotaen_US
dc.subjectMutational signatureen_US
dc.subject16S rRNAen_US
dc.titleCompositional and functional variations of oral microbiota associated with the mutational changes in oral canceren_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.oraloncology.2017.12.005en_US
dc.identifier.journalORAL ONCOLOGYen_US
dc.citation.volume77en_US
dc.citation.spage1en_US
dc.citation.epage8en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.department生物資訊及系統生物研究所zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.contributor.departmentInstitude of Bioinformatics and Systems Biologyen_US
dc.identifier.wosnumberWOS:000424850100001en_US
顯示於類別:期刊論文