Faculty Opinions recommendation of The Oral Microbiota May Have Influence on Oral Cancer.

Author(s):  
Michael Glogauer ◽  
Abdelahhad Barbour
Keyword(s):  
2020 ◽  
Author(s):  
Shih-Chi Su ◽  
Lun-Ching Chang ◽  
Hsien-Da Huang ◽  
Chih-Yu Peng ◽  
Chun-Yi Chuang ◽  
...  

Abstract Dysbiosis of oral microbiome may dictate the progression of oral squamous cell carcinoma (OSCC). Yet, the composition of oral microbiome fluctuates by saliva and distinct sites of oral cavity and is affected by risky behaviors (smoking, drinking and betel quid chewing) and individuals’ oral health condition. To characterize the disturbances in the oral microbial population mainly due to oral tumorigenicity, we profiled the bacteria within the surface of OSCC lesion and its contralateral normal tissue from discovery (n = 74) and validation (n = 42) cohorts of male patients with cancers of the buccal mucosa. Significant alterations in the bacterial diversity and relative abundance of specific oral microbiota (most profoundly, an enrichment for genus Fusobacterium and the loss of genus Streptococcus in the tumor sites) were identified. Functional prediction of oral microbiome shown that microbial genes related to the metabolism of terpenoids and polyketides were differentially enriched between the control and tumor groups, indicating a functional role of oral microbiome in formulating a tumor microenvironment via attenuated biosynthesis of secondary metabolites with anti-cancer effects. Furthermore, the vast majority of microbial signatures detected in the discovery cohort was generalized well to the independent validation cohort, and the clinical validity of these OSCC-associated microbes was observed and successfully replicated. Overall, our analyses reveal signatures (a profusion of Fusobacterium nucleatum CTI-2 and a decrease in Streptococcus pneumoniae) and functions (decreased production of tumor-suppressive metabolites) of oral microbiota related to oral cancer.


PLoS ONE ◽  
2014 ◽  
Vol 9 (6) ◽  
pp. e98741 ◽  
Author(s):  
Brian L. Schmidt ◽  
Justin Kuczynski ◽  
Aditi Bhattacharya ◽  
Bing Huey ◽  
Patricia M. Corby ◽  
...  
Keyword(s):  

2013 ◽  
Vol 38 (4) ◽  
pp. 181-188 ◽  
Author(s):  
Hee Sam Na ◽  
◽  
Seyeon Kim ◽  
Yoon Hee Choi ◽  
Ju-Yeon Lee ◽  
...  

2014 ◽  
Author(s):  
Donna G. Albertson ◽  
Justin Kuczynski ◽  
Aditi Bhattacharya ◽  
Bing Huey ◽  
Patricia M. Corby ◽  
...  
Keyword(s):  

2021 ◽  
Vol 11 ◽  
Author(s):  
Purandar Sarkar ◽  
Samaresh Malik ◽  
Sayantan Laha ◽  
Shantanab Das ◽  
Soumya Bunk ◽  
...  

Infection with specific pathogens and alterations in tissue commensal microbial composition are intricately associated with the development of many human cancers. Likewise, dysbiosis of oral microbiome was also shown to play critical role in the initiation as well as progression of oral cancer. However, there are no reports portraying changes in oral microbial community in the patients of Indian subcontinent, which has the highest incidence of oral cancer per year, globally. To establish the association of bacterial dysbiosis and oral squamous cell carcinoma (OSCC) among the Indian population, malignant lesions and anatomically matched adjacent normal tissues were obtained from fifty well-differentiated OSCC patients and analyzed using 16S rRNA V3-V4 amplicon based sequencing on the MiSeq platform. Interestingly, in contrast to the previous studies, a significantly lower bacterial diversity was observed in the malignant samples as compared to the normal counterpart. Overall our study identified Prevotella, Corynebacterium, Pseudomonas, Deinococcus and Noviherbaspirillum as significantly enriched genera, whereas genera including Actinomyces, Sutterella, Stenotrophomonas, Anoxybacillus, and Serratia were notably decreased in the OSCC lesions. Moreover, we demonstrated HPV-16 but not HPV-18 was significantly associated with the OSCC development. In future, with additional validation, this panel could directly be applied into clinical diagnostic and prognostic workflows for OSCC in Indian scenario.


2019 ◽  
Vol 61 (2) ◽  
pp. 120-128 ◽  
Author(s):  
Yasuharu Takahashi ◽  
Jonguk Park ◽  
Koji Hosomi ◽  
Tomonori Yamada ◽  
Ayaka Kobayashi ◽  
...  

Oral Oncology ◽  
2018 ◽  
Vol 77 ◽  
pp. 1-8 ◽  
Author(s):  
Shun-Fa Yang ◽  
Hsien-Da Huang ◽  
Wen-Lang Fan ◽  
Yuh-Jyh Jong ◽  
Mu-Kuan Chen ◽  
...  
Keyword(s):  

Author(s):  
Ling Zhang ◽  
Yuan Liu ◽  
Hua Jun Zheng ◽  
Chen Ping Zhang
Keyword(s):  

2020 ◽  
Vol 14 (2) ◽  
Author(s):  
Mariam Z. Kakabadze ◽  
Teona Paresishvili ◽  
Lia Karalashvili ◽  
David Chakhunashvili ◽  
Zurab Kakabadze

In this review, we draw attention and discuss the risk factors and causes of the development of oral squamous cell carcinoma (OSCC) focusing on oral microbiota. Recently, a breakthrough in the study of cancer has been the discovery of the relationship between the presence of certain types of bacteria and the development of cancer in the human body. Studies have shown that, Porphyromonas gingivalis (P. gingivalis) bacteria that is responsible for the destructive processes in the oral cavity, could play an important role in the development of OSCC. In our continuing search for bacteria that causes oral squamous cell carcinoma, we came across the Pseudomona aeruginosa, which due to its metabolite properties, may play important role in carcinogenesis of oral cancer. One possible mechanism is the ability of Pseudomonas to synthesize nitric oxide (NO) that modulates different cancer-related appearances such as apoptosis, cell cycle, angiogenesis, invasion, and metastasis. We think that P. aeruginosa increases the concentration of NO by converting salivary nitrite to nitric oxide, and this is how it contributes to NO-related carcinogenesis. Early diagnosis and treatment of periodontitis are very important not only for patients’ oral health, but also for the prevention of OSCC development. Screening test for OSCC based on determination of salivary NO levels could be appealing and may prove to be useful assay for diagnosis and early detection of disease progression in oral cancer.


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