Oral Microbiota Community Dynamics Associated With Oral Squamous Cell Carcinoma Staging

被引:258
作者
Yang, Chia-Yu [1 ,2 ,3 ,4 ]
Yeh, Yuan-Ming [3 ,5 ]
Yu, Hai-Ying [6 ]
Chin, Chia-Yin [3 ]
Hsu, Chia-Wei [3 ]
Liu, Hsuan [2 ,3 ,4 ,7 ]
Huang, Po-Jung [2 ,3 ,5 ,8 ]
Hu, Song-Nian [6 ]
Liao, Chun-Ta [9 ]
Chang, Kai-Ping [3 ,9 ]
Chang, Yu-Liang [10 ]
机构
[1] Chang Gung Univ, Dept Microbiol & Immunol, Coll Med, Taoyuan, Taiwan
[2] Chang Gung Univ, Grad Inst Biomed Sci, Coll Med, Taoyuan, Taiwan
[3] Chang Gung Univ, Mol Med Res Ctr, Taoyuan, Taiwan
[4] Chang Gung Mem Hosp, Div Colon & Rectal Surg, Linkou, Taiwan
[5] Chang Gung Mem Hosp, Genom Med Core Lab, Linkou, Taiwan
[6] Chinese Acad Sci, Beijing Inst Genom, CAS Key Lab Genome Sci & Informat, Beijing, Peoples R China
[7] Chang Gung Univ, Dept Cell & Mol Biol, Coll Med, Taoyuan, Taiwan
[8] Chang Gung Univ, Dept Biomed Sci, Coll Med, Taoyuan, Taiwan
[9] Chang Gung Mem Hosp, Dept Otolaryngol Head & Neck Surg, Taoyuan, Taiwan
[10] Chang Gung Mem Hosp, Dept Oral & Maxillofacial Surg, Taoyuan, Taiwan
关键词
oral microbiome; complexity; community dysbiosis; cancer progression; 16S rRNA sequencing; FILIFACTOR-ALOCIS; BACTERIA PRESENT; HEAD; PHARYNGEAL; DRINKING; PATHOGEN; SMOKING;
D O I
10.3389/fmicb.2018.00862
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Oral squamous cell carcinoma (OSCC) is a highly aggressive cancer and the fourth leading malignancy among males in Taiwan. Some pathogenic bacteria are associated with periodontitis and oral cancer. However, the comprehensive profile of the oral microbiome during the cancer's progression from the early stage to the late stage is still unclear. We profiled the oral microbiota and identified bacteria biomarkers associated with OSCC. The microbiota of an oral rinse from 51 healthy individuals and 197 OSCC patients at different stages were investigated using 16S rRNA V3V4 amplicon sequencing, followed by bioinformatics and statistical analyses. The oral microbiota communities from stage 4 patients showed significantly higher complexity than those from healthy controls. The populations also dynamically changed with the cancer's progression from stage 1 to stage 4. The predominant phyla in the oral samples showed variation in the relative abundance of Fusobacteria, Bacteroidetes, and Actinobacteria. The abundance of Fusobacteria increased significantly with the progression of oral cancer from the healthy controls (2.98%) to OSCC stage 1 (4.35%) through stage 4 (7.92%). At the genus level, the abundance of Fusobacterium increased, while the number of Streptococcus, Haemophilus, Porphyromonas, and Actinomyces decreased with cancer progression. Fusobacterium periodonticum, Parvimonas micra, Streptococcus constellatus, Haemophilus influenza, and Filifactor alocis were associated with OSCC, and they progressively increased in abundance from stage 1 to stage 4. The abundances of Streptococcus mitis, Haemophilus parainfluenzae, and Porphyromonas pasteri were inversely associated with OSCC progression. We selected a bacterial-marker panel of three bacteria (upregulated F. periodonticum, down-regulated S. mitis, and P. pasteri), which had an AUC of 0.956 (95% CI = 0.925-0.986) in discriminating OSCC stage 4 from the healthy controls. Furthermore, the functional prediction of oral bacterial communities showed that genes involved in carbohydrate-related metabolism, such as methane metabolism, and energy-metabolism-related parameters, such as oxidative phosphorylation and carbon fixation in photosynthetic organisms, were enriched in late-stage OSCC, while those responsible for amino acid metabolism, such as folate biosynthesis and valine, leucine, and isoleucine biosynthesis, were significantly associated with the healthy controls. In conclusion, our results provided evidence of oral bacteria community changes during oral cancer progression and suggested the possibility of using bacteria as OSCC diagnostic markers.
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页数:15
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