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Role of Oral Microbiome Signatures in Diagnosis and Prognosis of Oral Cancer
Open accessAbstract
Despite advancement in cancer treatment, oral cancer has a poor prognosis and is often detected at late stage. To overcome these challenges, investigators should search for early diagnostic and prognostic biomarkers. More than 700 bacterial species reside in the oral cavity. The oral microbiome population varies by saliva and different habitats of oral cavity. Tobacco, alcohol, and betel nut, which are causative factors of oral cancer, may alter the oral microbiome composition. Both pathogenic and commensal strains of bacteria have significantly contributed to oral cancer. Numerous bacterial species in the oral cavity are involved in chronic inflammation that lead to development of oral carcinogenesis. Bacterial products and its metabolic by-products may induce permanent genetic alterations in epithelial cells of the host that drive proliferation and/or survival of epithelial cells. Porphyromonas gingivalis and Fusobacterium nucleatum induce production of inflammatory cytokines, cell proliferation, and inhibition of apoptosis, cellular invasion, and migration thorough host cell genomic alterations. Recent advancement in metagenomic technologies may be useful in identifying oral cancer–related microbiome, their genomes, virulence properties, and their interaction with host immunity. It is very important to address which bacterial species is responsible for driving oral carcinogenesis. Alteration in the oral commensal microbial communities have potential application as a diagnostic tool to predict oral squamous cell carcinoma. Clinicians should be aware that the protective properties of the resident microflora are beneficial to define treatment strategies. To develop highly precise and effective therapeutic approaches, identification of specific oral microbiomes may be required. In this review, we narrate the role of microbiome in the progression of oral cancer and its role as an early diagnostic and prognostic biomarker for oral cancer.
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“Additional changes throughout one's life, including to dietary habits, age, hygiene regimens, and behaviors (such as tobacco and alcohol use), also influence changes to the oral microbiome.132”
From The oral microbiome: Role of key organisms and complex networks in oral health and disease (2021) · cites this paper as [132]
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Charlson, E. S., Chen, J., Custers-Allen, R., Bittinger, K., Li, H., Sinha, R., Hwang, J., Bushman, F. D., & Collman, R. G. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015216 · Cited by 437 · cited 1×
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“Fusobacterium nucleatum activates p38 which in turn activates HSP-27 and induces secretion of MMP-9 and MMP-13 (collagenase 3) that drive tumor invasion and metastasis.(9,103) Lipopolysaccharide of F nucleatum is involved in inflammation and cytokine-mediated damaging lesions of the GECs through the activation of tran…”
BackgroundTumor Cell Death and ATP Release Prime Dendritic Cells and Efficient Anticancer Immunity
Aymeric, L., Apétoh, L., Ghiringhelli, F., Tesnière, A., Martins, I., Kroemer, G., Smyth, M. J., & Zitvogel, L. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-3566 · Cited by 401
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Role of oral microbiome on oral cancers, a review
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“Smokers have unstable microbial colonization and are more susceptible to bacterial infection through alterations in innate and adaptive immune response.(83,84) Higher abundance of periodontopathogenic bacteria such as Prevotella tannerae, F nucleatum, and P intermedia and lower abundance of Streptococcus tigurinus wer…”
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Lee, W.-H., Chen, H., Yang, S., Liang, C., Peng, C.-Y., Lin, F.-M., Tsai, L., Wu, B.-C., Hsin, C., Chuang, C., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-16418-x · Cited by 230 · cited 1×
“Alistipes, Bacteroides, Blautia, Clostridium, Dorea, Escherichia, Faecalibacterium, Megamonas, and Phascolarctobacterium showed positive correlations between patients with epithelial precursor lesion and OSCC.(51) Furquim et al reported about the influence of salivary microbiome for developing Fanconi anemia (FA).”
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Perera, M. L., Al-Hebshi, N. N., Perera, I. R., Ipe, D. S., Ulett, G. C., Speicher, D. J., Chen, T., & Johnson, N. W. (2018) · Journal of Dental Research · doi:10.1177/0022034518767118 · Cited by 221 · cited 2×
“In OSCC, bacterial genes that encode enzymes such as transketolase, pyruvate formate lyase-activating enzyme, formate C-acetyltransferase, aspartokinase/homoserine dehydrogenase, and nitroreductase/dihydropteridine reductase were significantly overrepresented, whereas bacterial genes that encode iron complex transport…”
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“Aerobic and anaerobic bacteria together form oral biofilms that prevent changes in their environment.(11) The oral microbiome population varies with saliva and different habitats (buccal mucosa, supragingival, and subgingival plaque) of OC.”
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“Abundance of periodontal pathogens Fusobacterium, Prevotella, and Alloprevotella were progressively increased, whereas the abundance of Streptococcus was progressively decreased in progression of OSCC.(75) Numerous bacterial insertion sites were reported in host genes such as mycobacterium genomic element integrations…”
BackgroundPeriodontal Pathogens Produce Quorum Sensing Signal Molecules
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“Periodontal pathogens such as P gingivalis, P intermedia, and F nucleatum produce highest levels of AI-2.(26) The competence signaling peptide is responsible for the formation of biofilm, bacteriocins, stress response, acid tolerance, and genetic conversion by S mutans.”
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“Prevotella nanceiensis, Capnocytophaga leadbetteri, and Selenomonas sputigena were inversely related to HNSCC. Porphyromonas gingivalis, T forsythia, and A actinomycetemcomitans and S mutans were positively related to risk of HNSCC. Kingella dentificans and Streptococcus sanguinis were associated with reduced risk of…”
BackgroundInfluentialP. gingivalis accelerates gingival epithelial cell progression through the cell cycle
Kuboniwa, M., Hasegawa, Y., Mao, S., Shizukuishi, S., Amano, A., Lamont, R. J., & Yilmaz, Ö. (2007) · Microbes and Infection · doi:10.1016/j.micinf.2007.10.011 · Cited by 189 · cited 1×
“Porphyromonas gingivalis accelerates progression through the S-phase of the cell cycle by preventing activity of p53 tumor suppressor gene.(100) Induced expression of B7-H1 and B7-DC receptors on OSCC cells and primary GECs by P gingivalis has been reported earlier.”
BackgroundAcetaldehyde production from ethanol by oral streptococci
Kurkivuori, J., Salaspuro, V. J., Kaihovaara, P., Kari, K., Rautemaa‐Richardson, R., Grönroos, L., Meurman, J. H., & Salaspuro, M. P. (2006) · Oral Oncology · doi:10.1016/j.oraloncology.2006.02.005 · Cited by 188 · cited 1×
“Streptococcus salivarius, S intermedius, S mitis, and nonpathogenic Neisseria subspecies possess alcohol dehydrogenase (ADH) that is responsible for the production of carcinogenic compounds such as ALD, hydroxyl ethyl radicals, and hydroxyl radicals from ethanol.(80,81) Streptococcus anginosus was frequently reported…”
BackgroundShi, B., Chang, M., Martin, J. C., Mitreva, M., Lux, R., Klokkevold, P. R., Sodergren, E. J., Weinstock, G. M., Haake, S. K., & Li, H. (2015) · mBio · doi:10.1128/mbio.01926-14 · Cited by 179 · cited 1×
“Among them, Peptostreptococcus is known to be a potential pathogen for periodontitis.(45) Prevotella intermedia, F nucleatum, Selenomonas noxia, A actinomycetemcomitans, and Eubacterium nodatum, P gingivalis, T denticola, and T forsythia were also associated with pathogenesis of periodontal disease.”
BackgroundMicrobial diversity in saliva of oral squamous cell carcinoma
Pushalkar, S., Mane, S. P., Ji, X., Li, Y., Evans, C., Crasta, O. R., Morse, D. E., Meagher, R. J., Singh, A. K., & Saxena, D. B. (2010) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2010.00773.x · Cited by 178 · cited 2×
“Presence of Clavibacter michiganensis, Plantibacter flavus, Tepidimonas aquatica, and Thermus scotoductus were predominant in deep tumor tissues.(71) Exiguobacterium oxidotolerans, C gingivalis, P melaninogenica, Staphylococcus aureus, Veillonella parvula, Capnocytophaga ochracea, Eubacterium saburreum, L buccalis, an…”
BackgroundCarcinogenesis mechanisms of Fusobacterium nucleatum
Gholizadeh, P., Eslami, H., & Kafil, H. S. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.02.102 · Cited by 175 · cited 2×
“Fusobacterium nucleatum in GECs activates NLRP3 inflammasome that includes HMGB1 (high-morbidity group box-1 protein), apoptosis-associated speck-like protein, and caspase-1.(37) FadA adhesion molecule of F nucleatum binds to E-cadherin and activates b-catenin signaling that regulates cell proliferation and inflammato…”
BackgroundBetel nut chewing, oral premalignant lesions, and the oral microbiome
Hernandez, B. Y., Zhu, X., Goodman, M. T., Gatewood, R. R., Mendiola, P., Quinata, K. M. G., & Paulino, Y. C. (2017) · PLoS ONE · doi:10.1371/journal.pone.0172196 · Cited by 174 · cited 2×
“It has been reported that b diversity significantly differed between chewers and nonchewers with excessive alcohol consumption.(61) Smokers have more bacterial diversity in OP region when compared to nonsmokers.”
BackgroundZhu, X., Yang, X., Chao, Y., Zheng, H., Sheng, H.-F., Liu, H., He, Y., & Zhou, H. (2017) · EBioMedicine · doi:10.1016/j.ebiom.2017.02.002 · Cited by 170 · cited 1×
“Streptococcus mitis induces the breakdown of mucus in the human OC that drive translocation of pathogen into the lamina propria and recruitment of inflammatory cells.(114) Radiotherapy is used for the treatment of head and neck cancer.”
BackgroundAntimicrobial Defense Systems in Saliva
Hof, W. V. ‘., Veerman, E. C. I., Amerongen, A. V. N., & Ligtenberg, A. J. M. (2014) · Monographs in oral science · doi:10.1159/000358783 · Cited by 166
Yilmaz, Ö., Yao, L., Maeda, K., Rose, T. M., Lewis, E. L., Duman, M., Lamont, R. J., & Ojcius, D. M. (2008) · Cellular Microbiology · doi:10.1111/j.1462-5822.2007.01089.x · Cited by 165 · cited 1×
“Nucleoside diphosphate kinase of P gingivalis inhibits apoptosis and promotes survival of host epithelial cells.(97) Porphyromonas gingivalis reduces ATP activation of P2X7 receptors on dendritic cells that disrupt activation of the NLRP3/ASC/caspase-1 inflammasome.”
BackgroundA molecular analysis of the bacteria present within oral squamous cell carcinoma.
Hooper, S., Crean, S., Fardy, M., Lewis, M., Spratt, D., Wade, W., & Wilson, M. (2007) · Journal of Medical Microbiology · doi:10.1099/jmm.0.46918-0 · Cited by 165 · cited 1×
“The existence of viable bacteria in deep parts of OSCC favored the hypothesis that bacteria survived in the tumor microenvironment.(69,70) The bacterial taxa Veillonella, Fusobacterium, Prevotella, Porphyromonas, Actinomyces, and Clostridium belonging anaerobes, and Haemophilus, Enterobacteriaceae, and Streptococcus s…”
BackgroundOral Microbiome: A New Biomarker Reservoir for Oral and Oropharyngeal Cancers
Lim, Y., Totsika, M., Morrison, M., & Punyadeera, C. (2017) · Theranostics · doi:10.7150/thno.21804 · Cited by 161 · cited 2×
“Changes in environmental conditions increase the potential of pathogenic bacteria to create oral diseases.(12) Tongue, buccal mucosa, supragingival and subgingival surfaces of the teeth, soft and hard palates, and saliva of OC may represent different ecological niches or habitats.”
BackgroundViable Bacteria Present within Oral Squamous Cell Carcinoma Tissue
Hooper, S. J., Crean, S. J., Lewis, M. A. O., Spratt, D. A., Wade, W. G., & Wilson, M. J. (2006) · Journal of Clinical Microbiology · doi:10.1128/jcm.44.5.1719-1725.2006 · Cited by 160 · cited 1×
“The existence of viable bacteria in deep parts of OSCC favored the hypothesis that bacteria survived in the tumor microenvironment.(69,70) The bacterial taxa Veillonella, Fusobacterium, Prevotella, Porphyromonas, Actinomyces, and Clostridium belonging anaerobes, and Haemophilus, Enterobacteriaceae, and Streptococcus s…”
BackgroundHealth-Associated Niche Inhabitants as Oral Probiotics: The Case of Streptococcus dentisani
López‐López, A., Camelo-Castillo, A. J., Ferrer, M. D., Simón‐Soro, Á., & Mira, Á. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00379 · Cited by 159 · cited 1×
“Bacteriocins of Streptococcus dentisani inhibit the growth of cariogenic bacterial species.(36) Antimicrobial peptides such as bacteriocins produced by S mutans and S salivarius in the OC kill other bacteria.”
BackgroundHsiao, J., Chang, C., Lee, W., Huang, C., Ou, C., Tsai, S., Chen, K.-C., Huang, J.-S., Wong, T.-Y., Lai, Y.-H., et al. (2018) · Carcinogenesis · doi:10.1093/carcin/bgy053 · Cited by 153 · cited 1×
“Higher percentage of P intermedia was reported in betel quid chewers and alcohol users, whereas higher abundance of F nucleatum was reported in smokers.(85) The relative abundances of Periodontopathogenic genera Porphyromonas, Tannerella, and Treponema showed no significant positive correlations with cytokine concentr…”
BackgroundBacterial toxins and cancer — a case to answer?
Lax, A. J. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1130 · Cited by 145 · cited 1×
“Bacterial products such as endotoxins (LPS), enzymes (eg, proteases, collagenases, fibrinolysin, and phospholipase), and metabolic byproducts (eg, H2S, ammonia, and fatty acids) may induce permanent genetic alterations in epithelial cells of the host that drive proliferation and/or survival of epithelial cells.(91) Mi…”
BackgroundYao, L., Jermanus, C., Barbetta, B., Choi, C., Verbeke, P., Ojcius, D. M., & Yilmaz, Ö. (2010) · Molecular Oral Microbiology · doi:10.1111/j.2041-1014.2010.00569.x · Cited by 145
Lee, J., Roberts, J. S., Atanasova, K. R., Chowdhury, N., Han, K., & Yilmaz, Ö. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00493 · Cited by 145 · cited 1×
“Snail, Slug, and b-catenin enhances expressions of Zeb1, Vimentin, and MMP-2, -7, and -9.(108) Microbial organisms induce immune inflammation response in host cells that enhances mutation rate in normal cells and triggers malignant transformation of normal cells of host.”
BackgroundPeriodontal diseases and risk of oral cancer in Southern India: Results from the HeNCe Life study
Laprise, C., Shahul, H. P., Madathil, S. A., ThekkePurakkal, A. S., Castonguay, G., Varghese, I., Shiraz, S., Allison, P. J., Schlecht, N. F., Rousseau, M., et al. (2016) · International Journal of Cancer · doi:10.1002/ijc.30201 · Cited by 144 · cited 1×
“Chronic periodontitis enhances the risk of oral premalignant lesions that lead to OSCC and oropharyngeal squamous cell carcinoma (OPSCC).(42) Periodontal bacteria such as P gingivalis, P intermedia, and F nucleatum are essential for developing OSCC.”
BackgroundPreliminary analysis of salivary microbiome and their potential roles in oral lichen planus
Wang, K., Lu, W., Tu, Q., Ge, Y., He, J., Zhou, Y., Gou, Y., Nostrand, J. D. V., Qin, Y., Li, J., et al. (2016) · Scientific Reports · doi:10.1038/srep22943 · Cited by 139 · cited 1×
“Treponema, Porphyromonas, Parvimonas, and Fusobacterium were considered as a core microbiota in periodontitis.(50) Abundance of Bacillus, Enterococcus, Parvimonas, Peptostreptococcus, and Slackia were significantly different between epithelial precursor lesion and OSCC.”
BackgroundBörnigen, D., Ren, B., Pickard, R. K. L., Li, J., Ozer, E. K., Hartmann, E. M., Xiao, W., Tickle, T. L., Rider, J. R., Gevers, D., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-17795-z · Cited by 137 · cited 1×
“Abundance level of S anginosus, Peptoniphilus, and Mycoplasma were significantly decreased in HPV-positive cancers.(64) Smokers have unstable microbial colonization and are more susceptible to bacterial infection through alterations in innate and adaptive immune response.”
BackgroundStreptococcus anginosus infection in oral cancer and its infection route
Sasaki, M., Yamaura, C., Ohara‐Nemoto, Y., Tajika, S., Kodama, Y., Ohya, T., Harada, R. M., & Kimura, S. (2005) · Oral Diseases · doi:10.1111/j.1601-0825.2005.01051.x · Cited by 134 · cited 1×
“Streptococcus anginosus was frequently reported in OSCC and caused DNA damage in oral mucosa due increased synthesis of NO and cyclooxygenase 2.(82) Overrepresentation of the commensal bacterial genera, Corynebacterium and Kingella, showed reduced risk of HNSCC.”
BackgroundGroeger, S. E., Domann, E., Gonzales, J. R., Chakraborty, T., & Meyle, J. (2011) · Immunobiology · doi:10.1016/j.imbio.2011.05.005 · Cited by 134 · cited 1×
“Expression of B7-H1 receptor induces immune evasion in oral cancers.(101) ERK1/2-Ets1, p38/HSP27, and PAR2/NF-KB pathways are activated by P gingivalis infection to induce the expression of pro-MMP-9.”
BackgroundProtective effect of salivary nitrate and microbial nitrate reductase activity against caries
Doel, J. J., Hector, M. P., Amirtham, C. V., Al‐Anzan, L. A., Benjamin, N., & Allaker, R. P. (2004) · European Journal Of Oral Sciences · doi:10.1111/j.1600-0722.2004.00153.x · Cited by 131 · cited 1×
“Nitrite that is produced by oral microbiome is further reduced to nitric oxide that prevents the growth of cariogenic bacteria.(14,30) Veillonella subspecies metabolizes lactate into weaker acids that reduce local pH, whereas Streptococcus subspecies and Actinomyces subspecies generate the alkali, ammonia, by cataboli…”
BackgroundGeng, F., Liu, J., Guo, Y., Li, C., Wang, H., Wang, H., Zhao, H., & Pan, Y. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00057 · Cited by 131 · cited 1×
“Long-term exposure of P gingivalis induces cell proliferation, migration, and invasion through regulation of tumor-related genes such as FLI1, GAS6, PDCD1LG2, CD274, and lncRNACCAT1.(111) Whether profiling of expression of these genes could be used as biomarkers remain to be investigated.”
BackgroundMicrobiomic differences in tumor and paired-normal tissue in head and neck squamous cell carcinomas
Wang, H., Funchain, P., Bebek, G., Altemus, J. B., Zhang, H., Niazi, F., Peterson, C., Lee, W. T., Burkey, B. B., & Eng, C. (2017) · Genome Medicine · doi:10.1186/s13073-017-0405-5 · Cited by 128 · cited 1×
“Actinomyces subspecies may inhibit tumorigenesis through the secretion protease inhibitors.(60) Genus Streptococcus, Dialister, and Veillonella can be used to segregate HNSCC from healthy individuals.”
BackgroundThe role of bacterial pathogens in cancer
Vogelmann, R., & Amieva, M. R. (2007) · Current Opinion in Microbiology · doi:10.1016/j.mib.2006.12.004 · Cited by 127 · cited 1×
“well as the contributor to carcinogenesis.(88,89) Lipopolysaccharide from a potential pathogen such as P gingivalis and F nucleatum is responsible for the activation immune system at the cellular level in periodontal diseases.”
BackgroundAssociation of periodontal disease with oral cancer: a meta-analysis
Yao, Q., Zhou, D., Peng, H., Ji, P., & Liu, D. (2014) · Tumor Biology · doi:10.1007/s13277-014-1951-8 · Cited by 127 · cited 1×
“Periodontal bacteria such as P gingivalis, P intermedia, and F nucleatum are essential for developing OSCC.(18,43,44) Periodontitis is associated with the subgingival microbiota such as Peptostreptococcus, Synergistes, Filifactor, Mycoplasma, and Olsenella.”
BackgroundYang, S., Huang, H., Fan, W., Jong, Y., Chen, M., Huang, C., Chuang, C., Kuo, Y., Chung, W., & Su, S. (2017) · Oral Oncology · doi:10.1016/j.oraloncology.2017.12.005 · Cited by 127 · cited 1×
“Bacterial flagella were considered as key inflammatory structures in regulating OSCC-related inflammation.(92) It has been reported that F nucleatum subspecies polymorphum, Campylobacter subspecies, and P aeruginosa showed significant association with OSCC, whereas S mitis, R mucilaginosa, and H parainfluenzae were th…”
BackgroundPreliminary characterization of the oral microbiota of Chinese adults with and without gingivitis
Huang, S. W., Yang, F., Zeng, X., Chen, J., Li, R., Wen, T., Li, C., Wei, W., Liu, J., Chen, L., et al. (2011) · BMC Oral Health · doi:10.1186/1472-6831-11-33 · Cited by 123 · cited 1×
“High prevalence of L buccalis was reported in Chinese patients with gingivitis and necrotizing ulcerative gingivitis.(38) Prevotella subspecies, Lactobacillus subspecies, Dialister subspecies, and Filifactor subspecies are related to pathogenesis and progression of dental caries.”
BackgroundHou, J. L., Zheng, H., Li, P., Liu, H., Zhou, H., & Yang, X. (2018) · Radiotherapy and Oncology · doi:10.1016/j.radonc.2018.04.023 · Cited by 122 · cited 1×
“Four genera Fusobacterium, Porphyromonas, Treponema, and Prevotella showed dynamic synchronous variations in their relative abundances during treatment.(113) Oral microbial community is altered in the patients with nasopharyngeal carcinoma (NPC) who develop mucositis due to radiotherapy (RT).”
BackgroundLim, Y., Fukuma, N. M., Totsika, M., Kenny, L., Morrison, M., & Punyadeera, C. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00267 · Cited by 119 · cited 1×
“A positive correlation between HPV infection and the abundance of Haemophilus and Gemella has also been reported in OP cancer.(66) The abundance of Capnocytophaga was significantly higher in patients with recurrent OSCC when compared to controls.”
ResultBacteriome and mycobiome associations in oral tongue cancer
Mukherjee, P. K., Wang, H., Retuerto, M., Zhang, H., Burkey, B. B., Ghannoum, M. A., & Eng, C. (2017) · Oncotarget · doi:10.18632/oncotarget.21921 · Cited by 117 · cited 2×
“Rothia, Streptococcus, and Prevotella produce oral ALD that promote oral carcinogenesis (Table 3).(57) Streptococcus, Neisseria, and Veillonella are considered as anti-inflammatory mediators, whereas Selenomonas, Parvimonas, and Campylobacter are considered as pro-inflammatory mediators.”
BackgroundResultDawes, C. (2003) · Archives of Oral Biology · doi:10.1016/s0003-9969(03)00014-1 · Cited by 112 · cited 1×
“Most of the bacteria in saliva are attached to exfoliated human epithelial cells.(15) Microorganisms are classified based on their oxygen requirements as obligate aerobes; obligate anaerobes such as Fusobacterium and Veillonella; facultative anaerobes such as Actinomyces and Streptococci; microaerophiles that grow bes…”
BackgroundTribble, G. D., Kerr, J., & Wang, B.-Y. (2013) · Future Microbiology · doi:10.2217/fmb.13.30 · Cited by 111 · cited 1×
“Microbial organisms induce immune inflammation response in host cells that enhances mutation rate in normal cells and triggers malignant transformation of normal cells of host.(109) The staining intensity of P gingivalis in gingival carcinoma tissues was significantly enhanced when compared to noninvasive bacteria suc…”
BackgroundThe Biofilm Community: Rebels with a Cause
Aruni, W., Dou, Y., Mishra, A., & Fletcher, H. M. (2015) · Current Oral Health Reports · doi:10.1007/s40496-014-0044-5 · Cited by 108 · cited 1×
“Subgingival biofilms are mainly dominated by gram-negative obligate anaerobes.(24) Gram-positive aerobic bacteria, such as Actinomyces subspecies and oral Streptococci (S intermedius and S oralis) are responsible for the initial colonization in teeth surfaces.”
BackgroundSklenicka, S., Gardiner, S. K., Dierks, E. J., Potter, B. E., & Bell, R. B. (2010) · Journal of Oral and Maxillofacial Surgery · doi:10.1016/j.joms.2009.11.016 · Cited by 104 · cited 1×
“The OSCC is often detected at late stage, and there is a high risk of having second primary tumors.(8) To overcome these challenges, investigators should search for early diagnostic and prognostic biomarkers.”
BackgroundGuerrero-Preston, R. E., White, J. R., Godoy‐Vitorino, F., Rodríguez-Hilario, A., Navarro, K., González, H., Michailidi, C., Jedlicka, A., Canapp, S., Bondy, J., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.20677 · Cited by 98 · cited 13×
“Lactobacillus gasseri/ L johnsonii, H parainfluenza, L fermentum, and F periodonticum can be used as a diagnostic biomarker for HNSCC.(55) Reduction in levels of Lactobacillus subspecies induces microbial dysbiosis in patients with tongue cancer.”
BackgroundInfluentialChronic Periodontitis−Human Papillomavirus Synergy in Base of Tongue Cancers
Tezal, M., Nasca, M. A. S., Stoler, D. L., Melendy, T., Hyland, A. J., Smaldino, P. J., Rigual, N., & Loree, T. R. (2009) · Archives of Otolaryngology - Head and Neck Surgery · doi:10.1001/archoto.2009.6 · Cited by 96
Scarantino, C. W., LeVeque, F. G., Swann, R. S., White, R. L., Schulsinger, A., Hodson, D. I., Meredith, R. F., Foote, R. L., Brachman, D. G., & Lee, N. (2006) · PubMed · Cited by 94
Smoking decreases structural and functional resilience in the subgingival ecosystem
Joshi, V., Matthews, C. R., Aspiras, M., de Jager, M., Ward, M. T., & Kumar, P. (2014) · Journal Of Clinical Periodontology · doi:10.1111/jcpe.12300 · Cited by 91 · cited 1×
“Streptococcus, Neisseria, and Veillonella are considered as anti-inflammatory mediators, whereas Selenomonas, Parvimonas, and Campylobacter are considered as pro-inflammatory mediators.(93) Role of P gingivalis and F nucleatum in Progression of OSCC”
BackgroundNovel pathogens in periodontal microbiology
Hiranmayi, K. V., Sirisha, K., Rao, M. R., & Sudhakar, P. (2017) · Journal of Pharmacy And Bioallied Sciences · doi:10.4103/jpbs.jpbs_288_16 · Cited by 89 · cited 1×
“Synergistes are responsible for microecological changes and anaerobiosis in periodontal pocket, inflammation, and destruction of gingival tissue that may drive periodontitis-mediated oral carcinogenesis.(74) Mycoplasma, Treponema, Campylobacter, Eikenella, Fusobacterium, Selenomonas, Dialister, Peptostreptococcus, Fil…”
BackgroundMicrobial Signatures Associated with Oropharyngeal and Oral Squamous Cell Carcinomas
Banerjee, S., Tian, T., Wei, Z., Peck, K. N., Shih, N. N. C., Chalian, A. A., O’Malley, B. W., Weinstein, G. S., Feldman, M. D., Alwine, J. C., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-03466-6 · Cited by 85 · cited 1×
“These may drive tumorigenesis by altering gene expression.(76)”
BackgroundProfiling of Oral Microbiota in Early Childhood Caries Using Single-Molecule Real-Time Sequencing
Wang, Y., Zhang, J., Chen, X., Jiang, W. H., Wang, S., Xu, L., Tu, Y., Zheng, P., Wang, Y., Lin, X., et al. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.02244 · Cited by 80 · cited 1×
“Prevotella subspecies, Lactobacillus subspecies, Dialister subspecies, and Filifactor subspecies are related to pathogenesis and progression of dental caries.(39) The genera Veillonella, Bifidobacterium, Chattopadhyay et al 5”
BackgroundBashir, A., Miskeen, A. Y., Bhat, A., Fazili, K. M., & Ganai, B. A. (2015) · European Journal of Cancer Prevention · doi:10.1097/cej.0000000000000116 · Cited by 79 · cited 1×
“Fusobacterium nucleatum synergistically with other bacteria fungi and viruses may induce proinflammatory microenvironment through recruitment of tumor-infiltrating immune cells that favor tumorigenesis.(106) Antigens of P gingivalis have also been detected in gingival squamous carcinoma.”
BackgroundShaikh, M. H., McMillan, N. A. J., & Johnson, N. W. (2015) · Cancer Epidemiology · doi:10.1016/j.canep.2015.09.013 · Cited by 77 · cited 1×
“Human papilloma virus (HPV) infection is another known risk factor for oropharyngeal cancer (OPC).(5) Bacterial infection is one of the major causes of chronic inflammation which facilitates increased cell proliferation, mutagenesis, oncogene activation, and angiogenesis that lead to development of oral cancer.”
BackgroundDifferent frequencies of Porphyromonas gingivalis infection in cancers of the upper digestive tract
Yuan, X., Liu, Y., Kong, J., Gu, B., Qi, Y., Wang, X., Sun, M., Chen, P., Sun, W., Wang, H., et al. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.07.003 · Cited by 75 · cited 1×
“Porphyromonas gingivalis is considered as a potential risk factor for oral cancer.(107) Infection of P gingivalis induces EMT by downregulation of E-cadherin and nucleocytoplasmic accumulation of b-catenin that drive aggressiveness and/or metastatic potential in OSCC.”
BackgroundSingleton, D. R., Adrion, A. C., & Aitken, M. D. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-016-7867-z · Cited by 74 · cited 1×
“Terrimonas is involved in tumorigenic anthracene degradation.(87)”
Microbial and inflammatory‐based salivary biomarkers of head and neck squamous cell carcinoma
Vesty, A., Gear, K., Biswas, K., Radcliff, F. J., Taylor, M. W., & Douglas, R. G. (2018) · Clinical and Experimental Dental Research · doi:10.1002/cre2.139 · Cited by 71 · cited 1×
“The relative abundances of Periodontopathogenic genera Porphyromonas, Tannerella, and Treponema showed no significant positive correlations with cytokine concentrations.(86) Porphyromonas gingivalis, P intermedia, A actinomycetemcomitans, and F nucleatum are responsible to produce volatile sulfur compounds such as gen…”
BackgroundPan, C., Xu, X., Tan, L., Lin, L., & Pan, Y. (2013) · Oral Diseases · doi:10.1111/odi.12081 · Cited by 70
Gaetti‐Jardim, E., Gaetti-Jardim, E. C., Schweitzer, C. M., da Silva, J. C. L., Oliveira, M. M., Masocatto, D. C., & dos Santos, C. M. (2018) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2018.01.003 · Cited by 61 · cited 1×
“induces inflammation through the release of IL-1 and IL-6 in RT-induced mucositis.(115)”
BackgroundThe Salivary Microbiome and Oral Cancer Risk: A Pilot Study in Fanconi Anemia
Furquim, C. P., Soares, G. M. S., Ribeiro, L. L., Azcárate-Peril, M. A., Butz, N., Roach, J. M., MOSS, K. L., Bonfim, C., Torres‐Pereira, C. C., & Teles, F. (2016) · Journal of Dental Research · doi:10.1177/0022034516678169 · Cited by 60 · cited 1×
“The salivary microbiome profile of patients with FA showed similar diversity pattern with oral leukoplakia and OSCC.(52) 6 Technology in Cancer Research & Treatment”
BackgroundAl-Hebshi, N. N., Alharbi, F. A., Mahri, M., & Chen, T. (2017) · Genes · doi:10.3390/genes8040106 · Cited by 60 · cited 1×
“Oral taxon 44, and F nucleatum subspecies polymorphum are associated with OSCC.(68) Moraxella osloensis, Prevotella veroralis, and species of Actinomyces were only detected in normal tissues.”
BackgroundOral bacterial flora and oral cancer: The possible link?
Gaonkar, P. P., Patankar, S. R., Tripathi, N., & Sridharan, G. (2018) · Journal of Oral and Maxillofacial Pathology · doi:10.4103/jomfp.jomfp_89_16 · Cited by 50 · cited 1×
“Oral microbiome may function as synergistic risk factors along with primary risk factors such as alcohol and tobacco use.(77) Leukoplakia, erythroplakia, and oral submucous fibrosis are precursor lesion of oral cancer in betel nut chewers.”
BackgroundEffects of quorum sensing on cell viability in Streptococcus mutans biofilm formation
Zhang, K., Ou, M., Wang, W., & Ling, J. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.12.175 · Cited by 47 · cited 1×
“The competence signaling peptide is responsible for the formation of biofilm, bacteriocins, stress response, acid tolerance, and genetic conversion by S mutans.(27) Commensal bacteria live in equilibrium with the host immune response.”
BackgroundSintim, H. O., & Gürsoy, U. K. (2015) · OMICS A Journal of Integrative Biology · doi:10.1089/omi.2015.0146 · Cited by 42 · cited 2×
“Antimicrobial peptides such as bacteriocins produced by S mutans and S salivarius in the OC kill other bacteria.(25)”
BackgroundZhou, J., Jiang, N., Wang, S., Hu, X., Jiao, K., He, X., Li, Z., & Wang, J. (2016) · PLOS ONE · doi:10.1371/journal.pone.0147039 · Cited by 41 · cited 1×
“Veillonella has cariogenic potential and allows acidogenic bacteria such as Streptococcus species to grow and continue to produce additional acid.(40)”
BackgroundContribution of Plasminogen Activation towards the Pathogenic Potential of Oral Streptococci
Itzek, A., Gillen, C. M., Fulde, M., Friedrichs, C., Rodloff, A. C., Chhatwal, G. S., & Nitsche-Schmitz, D. P. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013826 · Cited by 32 · cited 1×
“Streptococcus is commonly found genera in the human OC, but it is highly genetically heterogeneous group.(19) Veillonella atypica, P gingivalis, Selenomonas subspecies, Actinobacillus actinomycetemcomitans, Prevotella intermedia, and Capnocytophaga are observed in tongue, whereas Streptococcus pyogenes, Streptococcus…”
BackgroundSalivary microbiome of an urban Indian cohort and patterns linked to subclinical inflammation
Acharya, A., Chan, Y., Kheur, S. M., Kheur, M. G., Gopalakrishnan, D., Watt, R., & Mattheos, N. (2017) · Oral Diseases · doi:10.1111/odi.12676 · Cited by 32 · cited 2×
“Abundance of Alphaproteobacteria and Deltaproteobacteria in saliva were higher in Indians when compared to HMP.(33) Streptococcus subspecies was the commonly observed bacterial genus in saliva of Indian populations.”
ResultPurinergic signaling during Porphyromonas gingivalis infection
Almeida-da-Silva, C. L. C., Morandini, A. C., Ulrich, H., Ojcius, D. M., & Coutinho‐Silva, R. (2016) · Biomedical Journal · doi:10.1016/j.bj.2016.08.003 · Cited by 29
Unraveling the human salivary microbiome diversity in Indian populations
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Sedghi, L., DiMassa, V., Harrington, A., Lynch, S. V., & Kapila, Y. L. (2021) · Periodontology 2000 · doi:10.1111/prd.12393 · Cited by 755
Oral microbiota and cancer development
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Oral–Gut Microbiome Axis in Gastrointestinal Disease and Cancer
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The Role of Fusobacterium nucleatum in Oral and Colorectal Carcinogenesis
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Metadata
- Authors
- Chattopadhyay, I., Verma, M., & Panda, M.
- Affiliations
- Central University of Tamil Nadu (IN)
- National Institutes of Health (US)
- Corresponding author
- Chattopadhyay, Indranil
- Venue
- Technology in Cancer Research & Treatment
- Publisher
- SAGE Publications
- Published
- 2019-01-01
- Volume
- 18
- Pages
- 1533033819867354-1533033819867354
- ISSN
- 1533-0338 (ISSN-L)
- 1533-0346
- PMC
- PMC6676258
- OpenAlex
- W2965423269
- Cited by
- 407
- References
- 118
- Citations by year
- 2026: 32 · 2025: 72 · 2024: 76 · 2023: 68 · 2022: 72 · 2021: 63 · 2020: 24
- FWCI
- 5.63
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Technology in Cancer Research & Treatment (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
- Health Sciences › Dentistry › General Dentistry › Oral Health Pathology and Treatment
- Health Sciences › Medicine › Otorhinolaryngology › Head and Neck Cancer Studies
- Keywords
- oral microbiota, oral cancer, oral squamous cell carcinoma, tumor markers, early diagnosis, prognosis, Porphyromonas gingivalis, Fusobacterium nucleatum, oral carcinogenesis, chronic inflammation, alcohol and tobacco use, areca nut, commensal bacteria, metagenomics, host-microbe interactions
- MeSH terms
- Humans, Inflammation, Mouth Neoplasms, Prognosis, Saliva, Porphyromonas gingivalis, Fusobacterium nucleatum, Cell Proliferation, Carcinogenesis, Microbiota
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