Systematic analyses uncover robust salivary microbial signatures and host-microbiome perturbations in oral squamous cell carcinoma

The oral cavity hosts a diverse microbial community that plays a crucial role in systemic and oral health. Accumulated research has investigated significant differences in the saliva microbiota associated with oral cancer, suggesting that microbiome dysbiosis may contribute to the pathogenesis of or...

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Published inmSystems Vol. 10; no. 2; p. e0124724
Main Authors Han, Zewen, Hu, Yichen, Lin, Xin, Cheng, Hongyu, Dong, Biao, Liu, Xuan, Wu, Buling, Xu, Zhenjiang Zech
Format Journal Article
LanguageEnglish
Published United States American Society for Microbiology 18.02.2025
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Abstract The oral cavity hosts a diverse microbial community that plays a crucial role in systemic and oral health. Accumulated research has investigated significant differences in the saliva microbiota associated with oral cancer, suggesting that microbiome dysbiosis may contribute to the pathogenesis of oral squamous cell carcinoma (OSCC). However, the specific microbial alterations linked to OSCC remain controversial. This meta-analysis reveals robust salivary microbiome alterations. Machine learning models using differential operational taxonomic units accurately predicted OSCC status, highlighting the potential of the salivary microbiome as a non-invasive diagnostic biomarker. Interestingly, age- and gender-associated signatures in the normal salivary microbiome were disrupted in OSCC, suggesting perturbations in host-microbe interactions.
AbstractList The oral cavity hosts a diverse microbial community that plays a crucial role in systemic and oral health. Accumulated research has investigated significant differences in the saliva microbiota associated with oral cancer, suggesting that microbiome dysbiosis may contribute to the pathogenesis of oral squamous cell carcinoma (OSCC). However, the specific microbial alterations linked to OSCC remain controversial. This meta-analysis reveals robust salivary microbiome alterations. Machine learning models using differential operational taxonomic units accurately predicted OSCC status, highlighting the potential of the salivary microbiome as a non-invasive diagnostic biomarker. Interestingly, age- and gender-associated signatures in the normal salivary microbiome were disrupted in OSCC, suggesting perturbations in host-microbe interactions.
ABSTRACT Oral squamous cell carcinoma (OSCC) is a prevalent malignancy in the oral-maxillofacial region with a poor prognosis. Oral microbiomes play a potential role in the pathogenesis of this disease. However, findings from individual studies have been inconsistent, and a comprehensive understanding of OSCC-associated microbiome dysbiosis remains elusive. Here, we conducted a large-scale meta-analysis by integrating 11 publicly available data sets comprising salivary microbiome profiles of OSCC patients and healthy controls. After correcting for batch effects, we observed significantly elevated alpha diversity and distinct beta-diversity patterns in the OSCC salivary microbiome compared to healthy controls. Leveraging random effects models, we identified robust microbial signatures associated with OSCC across data sets, including enrichment of taxa such as Streptococcus, Lactobacillus, Prevotella, Bulleidia moorei, and Haemophilus in OSCC samples. The machine learning models constructed from these microbial markers accurately predicted OSCC status, highlighting their potential as non-invasive diagnostic biomarkers. Intriguingly, our analyses revealed that the age- and gender-associated signatures in normal saliva microbiome were disrupted in the OSCC, suggesting perturbations in the intricate host-microbe interactions. Collectively, our findings uncovered complex alterations in the oral microbiome in OSCC, providing novel insights into disease etiology and paving the way for microbiome-based diagnostic and therapeutic strategies. Given that the salivary microbiome can reflect the overall health status of the host and that saliva sampling is a safe, non-invasive approach, it may be worthwhile to conduct broader screening of the salivary microbiome in high-risk OSCC populations as implications for early detection.IMPORTANCEThe oral cavity hosts a diverse microbial community that plays a crucial role in systemic and oral health. Accumulated research has investigated significant differences in the saliva microbiota associated with oral cancer, suggesting that microbiome dysbiosis may contribute to the pathogenesis of oral squamous cell carcinoma (OSCC). However, the specific microbial alterations linked to OSCC remain controversial. This meta-analysis reveals robust salivary microbiome alterations. Machine learning models using differential operational taxonomic units accurately predicted OSCC status, highlighting the potential of the salivary microbiome as a non-invasive diagnostic biomarker. Interestingly, age- and gender-associated signatures in the normal salivary microbiome were disrupted in OSCC, suggesting perturbations in host-microbe interactions.
ABSTRACTOral squamous cell carcinoma (OSCC) is a prevalent malignancy in the oral-maxillofacial region with a poor prognosis. Oral microbiomes play a potential role in the pathogenesis of this disease. However, findings from individual studies have been inconsistent, and a comprehensive understanding of OSCC-associated microbiome dysbiosis remains elusive. Here, we conducted a large-scale meta-analysis by integrating 11 publicly available data sets comprising salivary microbiome profiles of OSCC patients and healthy controls. After correcting for batch effects, we observed significantly elevated alpha diversity and distinct beta-diversity patterns in the OSCC salivary microbiome compared to healthy controls. Leveraging random effects models, we identified robust microbial signatures associated with OSCC across data sets, including enrichment of taxa such as Streptococcus, Lactobacillus, Prevotella, Bulleidia moorei, and Haemophilus in OSCC samples. The machine learning models constructed from these microbial markers accurately predicted OSCC status, highlighting their potential as non-invasive diagnostic biomarkers. Intriguingly, our analyses revealed that the age- and gender-associated signatures in normal saliva microbiome were disrupted in the OSCC, suggesting perturbations in the intricate host-microbe interactions. Collectively, our findings uncovered complex alterations in the oral microbiome in OSCC, providing novel insights into disease etiology and paving the way for microbiome-based diagnostic and therapeutic strategies. Given that the salivary microbiome can reflect the overall health status of the host and that saliva sampling is a safe, non-invasive approach, it may be worthwhile to conduct broader screening of the salivary microbiome in high-risk OSCC populations as implications for early detection.IMPORTANCEThe oral cavity hosts a diverse microbial community that plays a crucial role in systemic and oral health. Accumulated research has investigated significant differences in the saliva microbiota associated with oral cancer, suggesting that microbiome dysbiosis may contribute to the pathogenesis of oral squamous cell carcinoma (OSCC). However, the specific microbial alterations linked to OSCC remain controversial. This meta-analysis reveals robust salivary microbiome alterations. Machine learning models using differential operational taxonomic units accurately predicted OSCC status, highlighting the potential of the salivary microbiome as a non-invasive diagnostic biomarker. Interestingly, age- and gender-associated signatures in the normal salivary microbiome were disrupted in OSCC, suggesting perturbations in host-microbe interactions.
Oral squamous cell carcinoma (OSCC) is a prevalent malignancy in the oral-maxillofacial region with a poor prognosis. Oral microbiomes play a potential role in the pathogenesis of this disease. However, findings from individual studies have been inconsistent, and a comprehensive understanding of OSCC-associated microbiome dysbiosis remains elusive. Here, we conducted a large-scale meta-analysis by integrating 11 publicly available data sets comprising salivary microbiome profiles of OSCC patients and healthy controls. After correcting for batch effects, we observed significantly elevated alpha diversity and distinct beta-diversity patterns in the OSCC salivary microbiome compared to healthy controls. Leveraging random effects models, we identified robust microbial signatures associated with OSCC across data sets, including enrichment of taxa such as Streptococcus , Lactobacillus , Prevotella , Bulleidia moorei , and Haemophilus in OSCC samples. The machine learning models constructed from these microbial markers accurately predicted OSCC status, highlighting their potential as non-invasive diagnostic biomarkers. Intriguingly, our analyses revealed that the age- and gender-associated signatures in normal saliva microbiome were disrupted in the OSCC, suggesting perturbations in the intricate host-microbe interactions. Collectively, our findings uncovered complex alterations in the oral microbiome in OSCC, providing novel insights into disease etiology and paving the way for microbiome-based diagnostic and therapeutic strategies. Given that the salivary microbiome can reflect the overall health status of the host and that saliva sampling is a safe, non-invasive approach, it may be worthwhile to conduct broader screening of the salivary microbiome in high-risk OSCC populations as implications for early detection.
Oral squamous cell carcinoma (OSCC) is a prevalent malignancy in the oral-maxillofacial region with a poor prognosis. Oral microbiomes play a potential role in the pathogenesis of this disease. However, findings from individual studies have been inconsistent, and a comprehensive understanding of OSCC-associated microbiome dysbiosis remains elusive. Here, we conducted a large-scale meta-analysis by integrating 11 publicly available data sets comprising salivary microbiome profiles of OSCC patients and healthy controls. After correcting for batch effects, we observed significantly elevated alpha diversity and distinct beta-diversity patterns in the OSCC salivary microbiome compared to healthy controls. Leveraging random effects models, we identified robust microbial signatures associated with OSCC across data sets, including enrichment of taxa such as Streptococcus, Lactobacillus, Prevotella, Bulleidia moorei, and Haemophilus in OSCC samples. The machine learning models constructed from these microbial markers accurately predicted OSCC status, highlighting their potential as non-invasive diagnostic biomarkers. Intriguingly, our analyses revealed that the age- and gender-associated signatures in normal saliva microbiome were disrupted in the OSCC, suggesting perturbations in the intricate host-microbe interactions. Collectively, our findings uncovered complex alterations in the oral microbiome in OSCC, providing novel insights into disease etiology and paving the way for microbiome-based diagnostic and therapeutic strategies. Given that the salivary microbiome can reflect the overall health status of the host and that saliva sampling is a safe, non-invasive approach, it may be worthwhile to conduct broader screening of the salivary microbiome in high-risk OSCC populations as implications for early detection.IMPORTANCEThe oral cavity hosts a diverse microbial community that plays a crucial role in systemic and oral health. Accumulated research has investigated significant differences in the saliva microbiota associated with oral cancer, suggesting that microbiome dysbiosis may contribute to the pathogenesis of oral squamous cell carcinoma (OSCC). However, the specific microbial alterations linked to OSCC remain controversial. This meta-analysis reveals robust salivary microbiome alterations. Machine learning models using differential operational taxonomic units accurately predicted OSCC status, highlighting the potential of the salivary microbiome as a non-invasive diagnostic biomarker. Interestingly, age- and gender-associated signatures in the normal salivary microbiome were disrupted in OSCC, suggesting perturbations in host-microbe interactions.
Oral squamous cell carcinoma (OSCC) is a prevalent malignancy in the oral-maxillofacial region with a poor prognosis. Oral microbiomes play a potential role in the pathogenesis of this disease. However, findings from individual studies have been inconsistent, and a comprehensive understanding of OSCC-associated microbiome dysbiosis remains elusive. Here, we conducted a large-scale meta-analysis by integrating 11 publicly available data sets comprising salivary microbiome profiles of OSCC patients and healthy controls. After correcting for batch effects, we observed significantly elevated alpha diversity and distinct beta-diversity patterns in the OSCC salivary microbiome compared to healthy controls. Leveraging random effects models, we identified robust microbial signatures associated with OSCC across data sets, including enrichment of taxa such as Streptococcus, Lactobacillus, Prevotella, Bulleidia moorei, and Haemophilus in OSCC samples. The machine learning models constructed from these microbial markers accurately predicted OSCC status, highlighting their potential as non-invasive diagnostic biomarkers. Intriguingly, our analyses revealed that the age- and gender-associated signatures in normal saliva microbiome were disrupted in the OSCC, suggesting perturbations in the intricate host-microbe interactions. Collectively, our findings uncovered complex alterations in the oral microbiome in OSCC, providing novel insights into disease etiology and paving the way for microbiome-based diagnostic and therapeutic strategies. Given that the salivary microbiome can reflect the overall health status of the host and that saliva sampling is a safe, non-invasive approach, it may be worthwhile to conduct broader screening of the salivary microbiome in high-risk OSCC populations as implications for early detection.Oral squamous cell carcinoma (OSCC) is a prevalent malignancy in the oral-maxillofacial region with a poor prognosis. Oral microbiomes play a potential role in the pathogenesis of this disease. However, findings from individual studies have been inconsistent, and a comprehensive understanding of OSCC-associated microbiome dysbiosis remains elusive. Here, we conducted a large-scale meta-analysis by integrating 11 publicly available data sets comprising salivary microbiome profiles of OSCC patients and healthy controls. After correcting for batch effects, we observed significantly elevated alpha diversity and distinct beta-diversity patterns in the OSCC salivary microbiome compared to healthy controls. Leveraging random effects models, we identified robust microbial signatures associated with OSCC across data sets, including enrichment of taxa such as Streptococcus, Lactobacillus, Prevotella, Bulleidia moorei, and Haemophilus in OSCC samples. The machine learning models constructed from these microbial markers accurately predicted OSCC status, highlighting their potential as non-invasive diagnostic biomarkers. Intriguingly, our analyses revealed that the age- and gender-associated signatures in normal saliva microbiome were disrupted in the OSCC, suggesting perturbations in the intricate host-microbe interactions. Collectively, our findings uncovered complex alterations in the oral microbiome in OSCC, providing novel insights into disease etiology and paving the way for microbiome-based diagnostic and therapeutic strategies. Given that the salivary microbiome can reflect the overall health status of the host and that saliva sampling is a safe, non-invasive approach, it may be worthwhile to conduct broader screening of the salivary microbiome in high-risk OSCC populations as implications for early detection.The oral cavity hosts a diverse microbial community that plays a crucial role in systemic and oral health. Accumulated research has investigated significant differences in the saliva microbiota associated with oral cancer, suggesting that microbiome dysbiosis may contribute to the pathogenesis of oral squamous cell carcinoma (OSCC). However, the specific microbial alterations linked to OSCC remain controversial. This meta-analysis reveals robust salivary microbiome alterations. Machine learning models using differential operational taxonomic units accurately predicted OSCC status, highlighting the potential of the salivary microbiome as a non-invasive diagnostic biomarker. Interestingly, age- and gender-associated signatures in the normal salivary microbiome were disrupted in OSCC, suggesting perturbations in host-microbe interactions.IMPORTANCEThe oral cavity hosts a diverse microbial community that plays a crucial role in systemic and oral health. Accumulated research has investigated significant differences in the saliva microbiota associated with oral cancer, suggesting that microbiome dysbiosis may contribute to the pathogenesis of oral squamous cell carcinoma (OSCC). However, the specific microbial alterations linked to OSCC remain controversial. This meta-analysis reveals robust salivary microbiome alterations. Machine learning models using differential operational taxonomic units accurately predicted OSCC status, highlighting the potential of the salivary microbiome as a non-invasive diagnostic biomarker. Interestingly, age- and gender-associated signatures in the normal salivary microbiome were disrupted in OSCC, suggesting perturbations in host-microbe interactions.
Oral squamous cell carcinoma (OSCC) is a prevalent malignancy in the oral-maxillofacial region with a poor prognosis. Oral microbiomes play a potential role in the pathogenesis of this disease. However, findings from individual studies have been inconsistent, and a comprehensive understanding of OSCC-associated microbiome dysbiosis remains elusive. Here, we conducted a large-scale meta-analysis by integrating 11 publicly available data sets comprising salivary microbiome profiles of OSCC patients and healthy controls. After correcting for batch effects, we observed significantly elevated alpha diversity and distinct beta-diversity patterns in the OSCC salivary microbiome compared to healthy controls. Leveraging random effects models, we identified robust microbial signatures associated with OSCC across data sets, including enrichment of taxa such as , , , , and in OSCC samples. The machine learning models constructed from these microbial markers accurately predicted OSCC status, highlighting their potential as non-invasive diagnostic biomarkers. Intriguingly, our analyses revealed that the age- and gender-associated signatures in normal saliva microbiome were disrupted in the OSCC, suggesting perturbations in the intricate host-microbe interactions. Collectively, our findings uncovered complex alterations in the oral microbiome in OSCC, providing novel insights into disease etiology and paving the way for microbiome-based diagnostic and therapeutic strategies. Given that the salivary microbiome can reflect the overall health status of the host and that saliva sampling is a safe, non-invasive approach, it may be worthwhile to conduct broader screening of the salivary microbiome in high-risk OSCC populations as implications for early detection. The oral cavity hosts a diverse microbial community that plays a crucial role in systemic and oral health. Accumulated research has investigated significant differences in the saliva microbiota associated with oral cancer, suggesting that microbiome dysbiosis may contribute to the pathogenesis of oral squamous cell carcinoma (OSCC). However, the specific microbial alterations linked to OSCC remain controversial. This meta-analysis reveals robust salivary microbiome alterations. Machine learning models using differential operational taxonomic units accurately predicted OSCC status, highlighting the potential of the salivary microbiome as a non-invasive diagnostic biomarker. Interestingly, age- and gender-associated signatures in the normal salivary microbiome were disrupted in OSCC, suggesting perturbations in host-microbe interactions.
Author Hu, Yichen
Lin, Xin
Liu, Xuan
Wu, Buling
Han, Zewen
Dong, Biao
Cheng, Hongyu
Xu, Zhenjiang Zech
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Cites_doi 10.1016/j.chom.2019.06.013
10.1371/journal.pone.0194729
10.18632/oncotarget.20677
10.1001/jamaoncol.2017.4777
10.1038/s41591-019-0405-7
10.1136/gutjnl-2016-313189
10.3389/fmicb.2022.895537
10.1128/AEM.03006-05
10.1099/jmm.0.001417
10.1016/j.heliyon.2023.e13198
10.1128/mSystems.00191-16
10.1186/s12903-023-03760-y
10.1007/s00248-020-01596-5
10.1002/cre2.139
10.1001/jamanetworkopen.2020.17357
10.3389/fmicb.2018.00862
10.3322/caac.21660
10.1038/s41522-022-00279-y
10.1080/19490976.2023.2197835
10.1038/s41368-023-00249-w
10.1038/s41598-017-16418-x
10.1111/apm.13315
10.1186/s12866-020-01801-y
10.3389/fcimb.2021.728933
10.3389/fmicb.2021.719601
10.1111/jre.12691
10.1371/journal.pcbi.1004977
10.1016/B978-0-7020-3468-8.50201-7
10.1128/mSystems.00323-19
10.1186/s40168-023-01613-y
10.1016/j.jri.2021.103293
10.1038/s41388-021-02137-1
10.1186/gb-2010-11-10-r106
10.3390/ijms242015456
10.1038/s41392-022-00974-4
10.1177/21925682221110527
10.1080/20002297.2022.2051352
10.1038/s41598-020-59016-0
10.3389/fonc.2021.737843
10.3390/cancers15133270
10.1038/s41587-019-0209-9
10.5555/1953048.2078195
10.18637/jss.v036.i03
10.1111/jop.13546
10.18632/aging.103108
10.1038/s41579-023-00963-6
10.1128/mSystems.00630-19
10.1038/s41591-019-0406-6
10.1128/msystems.00738-22
10.1177/0022034520968750
10.1038/s41598-019-46790-9
10.1002/ijc.34460
10.1101/gr.276482.121
10.1038/s41467-022-33071-9
10.3389/fcimb.2022.942328
10.1128/spectrum.02737-22
10.1016/j.ctarc.2024.100831
10.1007/s42770-022-00721-5
10.1111/jop.13492
10.1007/s00784-020-03592-y
10.1002/advs.201902054
10.1016/j.isci.2022.105839
10.1128/mBio.03281-20
10.1038/s41598-019-52445-6
10.1007/s00253-022-11980-5
10.3389/fcimb.2021.663068
10.1016/j.bbapap.2021.140659
10.3389/fmicb.2022.968304
10.1111/odi.12341
10.1111/prd.12366
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Issue 2
Keywords meta-analysis
oral squamous cell carcinoma
gender
salivary microbiome
age
Language English
License This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license. https://creativecommons.org/licenses/by/4.0
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The authors declare no conflict of interest.
Zewen Han and Yichen Hu contributed equally to this article. Author order was determined by drawing straws.
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crossref_primary_10_1128_msystems_01247_24
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2025-02-18
PublicationDateYYYYMMDD 2025-02-18
PublicationDate_xml – month: 02
  year: 2025
  text: 2025-02-18
  day: 18
PublicationDecade 2020
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: 1752 N St., N.W., Washington, DC
– name: Washington
PublicationTitle mSystems
PublicationTitleAbbrev mSystems
PublicationTitleAlternate mSystems
PublicationYear 2025
Publisher American Society for Microbiology
Publisher_xml – name: American Society for Microbiology
References e_1_3_4_3_2
e_1_3_4_61_2
e_1_3_4_9_2
e_1_3_4_63_2
e_1_3_4_7_2
e_1_3_4_40_2
e_1_3_4_5_2
e_1_3_4_23_2
e_1_3_4_44_2
e_1_3_4_69_2
e_1_3_4_21_2
e_1_3_4_42_2
e_1_3_4_27_2
e_1_3_4_48_2
e_1_3_4_65_2
e_1_3_4_25_2
e_1_3_4_46_2
e_1_3_4_67_2
e_1_3_4_29_2
e_1_3_4_30_2
e_1_3_4_51_2
e_1_3_4_70_2
e_1_3_4_11_2
e_1_3_4_34_2
e_1_3_4_57_2
e_1_3_4_55_2
e_1_3_4_32_2
e_1_3_4_59_2
e_1_3_4_53_2
e_1_3_4_15_2
e_1_3_4_38_2
e_1_3_4_13_2
e_1_3_4_36_2
e_1_3_4_19_2
e_1_3_4_17_2
e_1_3_4_2_2
e_1_3_4_60_2
e_1_3_4_62_2
e_1_3_4_8_2
e_1_3_4_41_2
e_1_3_4_6_2
e_1_3_4_4_2
e_1_3_4_22_2
e_1_3_4_45_2
e_1_3_4_68_2
e_1_3_4_20_2
e_1_3_4_43_2
e_1_3_4_26_2
e_1_3_4_49_2
e_1_3_4_64_2
e_1_3_4_24_2
e_1_3_4_47_2
e_1_3_4_66_2
e_1_3_4_28_2
e_1_3_4_71_2
e_1_3_4_52_2
e_1_3_4_50_2
e_1_3_4_12_2
e_1_3_4_33_2
e_1_3_4_58_2
e_1_3_4_54_2
e_1_3_4_10_2
e_1_3_4_31_2
e_1_3_4_16_2
e_1_3_4_37_2
e_1_3_4_14_2
e_1_3_4_35_2
e_1_3_4_56_2
e_1_3_4_18_2
e_1_3_4_39_2
Sousa‐Neto, SS, Martins, AFL, Moreira, VHL de O, Pereira, JGB, Freitas, NMA, Curado, MP, Leles, CR, Mendonça, EF (B8) 2024; 53
Ling, W, Lu, J, Zhao, N, Lulla, A, Plantinga, AM, Fu, W, Zhang, A, Liu, H, Song, H, Li, Z, Chen, J, Randolph, TW, Koay, WLA, White, JR, Launer, LJ, Fodor, AA, Meyer, KA, Wu, MC (B39) 2022; 13
Hamada, M, Inaba, H, Nishiyama, K, Yoshida, S, Yura, Y, Matsumoto-Nakano, M, Uzawa, N (B66) 2023; 24
Tan, Y, Wang, Z, Xu, M, Li, B, Huang, Z, Qin, S, Nice, EC, Tang, J, Huang, C (B5) 2023; 15
González-Ruiz, I, Ramos-García, P, Ruiz-Ávila, I, González-Moles, MÁ (B9) 2023; 15
Lee, W-H, Chen, H-M, Yang, S-F, Liang, C, Peng, C-Y, Lin, F-M, Tsai, L-L, Wu, B-C, Hsin, C-H, Chuang, C-Y, Yang, T, Yang, T-L, Ho, S-Y, Chen, W-L, Ueng, K-C, Huang, H-D, Huang, C-N, Jong, Y-J (B20) 2017; 7
Tagaino, R, Washio, J, Abiko, Y, Tanda, N, Sasaki, K, Takahashi, N (B59) 2019; 9
Sawant, S, Dugad, J, Parikh, D, Srinivasan, S, Singh, H (B15) 2021; 70
Ye, E, Sun, H, Leone, MJ, Paixao, L, Thomas, RJ, Lam, AD, Westover, MB (B46) 2020; 3
Omori, M, Kato-Kogoe, N, Sakaguchi, S, Fukui, N, Yamamoto, K, Nakajima, Y, Inoue, K, Nakano, H, Motooka, D, Nakano, T, Nakamura, S, Ueno, T (B49) 2021; 25
Bolyen, E, Rideout, JR, Dillon, MR, Bokulich, NA, Abnet, CC, Al-Ghalith, GA, Alexander, H, Alm, EJ, Arumugam, M, Asnicar, F (B36) 2019; 37
Fan, X, Peters, BA, Min, D, Ahn, J, Hayes, RB (B48) 2018; 13
Stashenko, P, Yost, S, Choi, Y, Danciu, T, Chen, T, Yoganathan, S, Kressirer, C, Ruiz-Tourrella, M, Das, B, Kokaras, A, Frias-Lopez, J (B10) 2019; 4
Torralba, MG, Aleti, G, Li, W, Moncera, KJ, Lin, Y-H, Yu, Y, Masternak, MM, Golusinski, W, Golusinski, P, Lamperska, K, Edlund, A, Freire, M, Nelson, KE (B63) 2021; 82
Huang, S, Haiminen, N, Carrieri, A-P, Hu, R, Jiang, L, Parida, L, Russell, B, Allaband, C, Zarrinpar, A, Vázquez-Baeza, Y, Belda-Ferre, P, Zhou, H, Kim, H-C, Swafford, AD, Knight, R, Xu, ZZ (B31) 2020; 5
Viechtbauer, W (B43) 2010; 36
Pedregosa, F, Varoquaux, G, Gramfort, A, Michel, V, Thirion, B, Grisel, O, Blondel, M, Prettenhofer, P, Weiss, R, Dubourg, V, Vanderplas, J, Passos, A, Cournapeau, D, Brucher, M, Perrot, M, Duchesnay, E (B44) 2011; 12
Li, Y, Hu, YC, Zhan, X, Song, Y, Xu, M, Wang, SJ, Huang, XC, Xu, ZZ (B53) 2023; 15
Moritani, K, Takeshita, T, Shibata, Y, Ninomiya, T, Kiyohara, Y, Yamashita, Y (B58) 2015; 21
Hayes, RB, Ahn, J, Fan, X, Peters, BA, Ma, Y, Yang, L, Agalliu, I, Burk, RD, Ganly, I, Purdue, MP, Freedman, ND, Gapstur, SM, Pei, Z (B64) 2018; 4
Sung, H, Ferlay, J, Siegel, RL, Laversanne, M, Soerjomataram, I, Jemal, A, Bray, F (B6) 2021; 71
Pasolli, E, Truong, DT, Malik, F, Waldron, L, Segata, N (B45) 2016; 12
Zhou, X, Hao, Y, Peng, X, Li, B, Han, Q, Ren, B, Li, M, Li, L, Li, Y, Cheng, G, Li, J, Ma, Y, Zhou, X, Cheng, L (B22) 2021; 11
Jo, R, Nishimoto, Y, Umezawa, K, Yama, K, Aita, Y, Ichiba, Y, Murakami, S, Kakizawa, Y, Kumagai, T, Yamada, T, Fukuda, S (B47) 2019; 9
Zeng, B, Tan, J, Guo, G, Li, Z, Yang, L, Lao, X, Wang, D, Ma, J, Zhang, S, Liao, G, Liang, Y (B34) 2022; 12
Guerrero-Preston, R, White, JR, Godoy-Vitorino, F, Rodríguez-Hilario, A, Navarro, K, González, H, Michailidi, C, Jedlicka, A, Canapp, S, Bondy, J, Dziedzic, A, Mora-Lagos, B, Rivera-Alvarez, G, Ili-Gangas, C, Brebi-Mieville, P, Westra, W, Koch, W, Kang, H, Marchionni, L, Kim, Y, Sidransky, D (B60) 2017; 8
Kaan, AMM, Kahharova, D, Zaura, E (B26) 2021; 86
Wirbel, J, Pyl, PT, Kartal, E, Zych, K, Kashani, A, Milanese, A, Fleck, JS, Voigt, AY, Palleja, A, Ponnudurai, R (B54) 2019; 25
Hu, Y, Amir, A, Huang, X, Li, Y, Huang, S, Wolfe, E, Weiss, S, Knight, R, Xu, ZZ (B1) 2022; 32
Chan, JYK, Ng, CWK, Lan, L, Fung, S, Li, J-W, Cai, L, Lei, P, Mou, Q, Meehan, K, Lau, EHL, Yeung, Z, Chan, KCA, Wong, EWY, Chan, PKS, Chen, Z (B18) 2021; 11
Delaney, C, Veena, CLR, Butcher, MC, McLean, W, Shaban, SMA, Nile, CJ, Ramage, G (B69) 2023; 131
Baker, JL, Mark Welch, JL, Kauffman, KM, McLean, JS, He, X (B2) 2024; 22
Xu, H, Tian, B, Shi, W, Tian, J, Wang, W, Qin, M (B27) 2022; 14
Frank, DN, Qiu, Y, Cao, Y, Zhang, S, Lu, L, Kofonow, JM, Robertson, CE, Liu, Y, Wang, H, Levens, CL, Kuhn, KA, Song, J, Ramakrishnan, VR, Lu, S-L (B61) 2022; 41
Brook, I, Long, SS (B62) 2008
Yang, C-Y, Yeh, Y-M, Yu, H-Y, Chin, C-Y, Hsu, C-W, Liu, H, Huang, P-J, Hu, S-N, Liao, C-T, Chang, K-P, Chang, Y-L (B21) 2018; 9
Caselli, E, Fabbri, C, D’Accolti, M, Soffritti, I, Bassi, C, Mazzacane, S, Franchi, M (B50) 2020; 20
Burcham, ZM, Garneau, NL, Comstock, SS, Tucker, RM, Knight, R, Metcalf, JL, Miranda, A, Reinhart, B, Meyers, D, Woltkamp, D, Boxer, E, Hutchens, J, Kim, K, Archer, M, McAteer, M, Huss, P, Defonseka, R, Stahle, S, Babu, S, Nuessle, T, Schowinsky, V, Covert, W, Truman, W, Reusser, W (B28) 2020; 10
Liu, F, Lu, H, Dong, B, Huang, X, Cheng, H, Qu, R, Hu, Y, Zhong, L, Guo, Z, You, Y, Xu, ZZ (B70) 2023; 8
Vesty, A, Gear, K, Biswas, K, Radcliff, FJ, Taylor, MW, Douglas, RG (B19) 2018; 4
DeSantis, TZ, Hugenholtz, P, Larsen, N, Rojas, M, Brodie, EL, Keller, K, Huber, T, Dalevi, D, Hu, P, Andersen, GL (B38) 2006; 72
Huang, S, He, T, Yue, F, Xu, X, Wang, L, Zhu, P, Teng, F, Sun, Z, Liu, X, Jing, G, Su, X, Jin, L, Liu, J, Xu, J (B52) 2021; 12
Anders, S, Huber, W (B42) 2010; 11
Willis, JR, Saus, E, Iraola-Guzmán, S, Ksiezopolska, E, Cozzuto, L, Bejarano, LA, Andreu-Somavilla, N, Alloza-Trabado, M, Blanco, A, Puig-Sola, A, Broglio, E, Carolis, C, Ponomarenko, J, Hecht, J, Gabaldón, T (B51) 2022; 8
Bisanz, JE, Upadhyay, V, Turnbaugh, JA, Ly, K, Turnbaugh, PJ (B40) 2019; 26
Yang, K, Wang, Y, Zhang, S, Zhang, D, Hu, L, Zhao, T, Zheng, H (B17) 2021; 12
Wang, X, Mi, Q, Yang, J, Guan, Y, Zeng, W, Xiang, H, Liu, X, Yang, W, Yang, G, Li, X, Cui, Y, Gao, Q (B57) 2022; 53
Chen, MY, Chen, JW, Wu, LW, Huang, KC, Chen, JY, Wu, WS, Chiang, WF, Shih, CJ, Tsai, KN, Hsieh, WT, Ho, YH, Wong, TY, Wu, JH, Chen, YL (B35) 2021; 100
Lan, QY, Zhang, C, Hua, H, Hu, XS (B24) 2023; 23
Hou, K, Wu, Z-X, Chen, X-Y, Wang, J-Q, Zhang, D, Xiao, C, Zhu, D, Koya, JB, Wei, L, Li, J, Chen, Z-S (B3) 2022; 7
Thomas, AM, Manghi, P, Asnicar, F, Pasolli, E, Armanini, F, Zolfo, M, Beghini, F, Manara, S, Karcher, N, Pozzi, C (B55) 2019; 25
Chen, J-W, Wu, J-H, Chiang, W-F, Chen, Y-L, Wu, W-S, Wu, L-W (B14) 2021; 11
Srivastava, A, Mishra, S, Garg, PK, Dubey, AK, Deo, SVS, Verma, D (B13) 2022; 106
Liu, S, Wang, Y, Zhao, L, Sun, X, Feng, Q (B30) 2020; 12
Peter, TK, Withanage, MHH, Comnick, CL, Pendleton, C, Dabdoub, S, Ganesan, S, Drake, D, Banas, J, Xie, XJ, Zeng, E (B67) 2022; 13
Heng, W, Wang, W, Dai, T, Jiang, P, Lu, Y, Li, R, Zhang, M, Xie, R, Zhou, Y, Zhao, M, Duan, N, Ye, Z, Yan, F, Wang, X (B23) 2022; 10
Ma, ZS, Li, W (B33) 2019; 6
Saadaoui, M, Singh, P, Al Khodor, S (B29) 2021; 145
Mäkinen, AI, Pappalardo, VY, Buijs, MJ, Brandt, BW, Mäkitie, AA, Meurman, JH, Zaura, E (B25) 2023; 11
Frey‐Furtado, L, Magalhães, I, Sampaio‐Maia, B, Azevedo, MJ (B65) 2023; 52
Dettori, JR, Norvell, DC, Chapman, JR (B56) 2022; 12
Lafuente Ibáñez de Mendoza, I, Maritxalar Mendia, X, García de la Fuente, AM, Quindós Andrés, G, Aguirre Urizar, JM (B11) 2020; 55
Zhu, H, Yip, HC, Cheung, MK, Chan, HC, Ng, C, Lau, EHL, Yeung, ZWC, Wong, EWY, Leung, L, Qu, X, Wang, D, Cai, L, Chan, PKS, Chan, JYK, Chen, Z (B12) 2023; 152
Li, X, Liu, Y, Yang, X, Li, C, Song, Z (B4) 2022; 13
Swaminathan, D, George, NA, Thomas, S, Iype, EM (B7) 2024; 40
Granato, DC, Neves, LX, Trino, LD, Carnielli, CM, Lopes, AFB, Yokoo, S, Pauletti, BA, Domingues, RR, Sá, JO, Persinoti, G, Paixão, DAA, Rivera, C, de Sá Patroni, FM, Tommazetto, G, Santos-Silva, AR, Lopes, MA, de Castro, G, Brandão, TB, Prado-Ribeiro, AC, Squina, FM, Telles, GP, Paes Leme, AF (B16) 2021; 1869
Liu, X, Tong, X, Jie, Z, Zhu, J, Tian, L, Sun, Q, Ju, Y, Zou, L, Lu, H, Qiu, X (B32) 2023; 26
Amir, A, McDonald, D, Navas-Molina, JA, Kopylova, E, Morton, JT, Zech Xu, Z, Kightley, EP, Thompson, LR, Hyde, ER, Gonzalez, A, Knight, R (B37) 2017; 2
Yu, X, Shi, Y, Yuan, R, Chen, Z, Dong, Q, Han, L, Wang, L, Zhou, J (B68) 2023; 9
Shah, MS, DeSantis, TZ, Weinmaier, T, McMurdie, PJ, Cope, JL, Altrichter, A, Yamal, JM, Hollister, EB (B41) 2018; 67
References_xml – ident: e_1_3_4_41_2
  doi: 10.1016/j.chom.2019.06.013
– ident: e_1_3_4_49_2
  doi: 10.1371/journal.pone.0194729
– ident: e_1_3_4_61_2
  doi: 10.18632/oncotarget.20677
– ident: e_1_3_4_65_2
  doi: 10.1001/jamaoncol.2017.4777
– ident: e_1_3_4_56_2
  doi: 10.1038/s41591-019-0405-7
– ident: e_1_3_4_42_2
  doi: 10.1136/gutjnl-2016-313189
– ident: e_1_3_4_5_2
  doi: 10.3389/fmicb.2022.895537
– ident: e_1_3_4_39_2
  doi: 10.1128/AEM.03006-05
– ident: e_1_3_4_16_2
  doi: 10.1099/jmm.0.001417
– ident: e_1_3_4_69_2
  doi: 10.1016/j.heliyon.2023.e13198
– ident: e_1_3_4_38_2
  doi: 10.1128/mSystems.00191-16
– ident: e_1_3_4_25_2
  doi: 10.1186/s12903-023-03760-y
– ident: e_1_3_4_64_2
  doi: 10.1007/s00248-020-01596-5
– ident: e_1_3_4_20_2
  doi: 10.1002/cre2.139
– ident: e_1_3_4_47_2
  doi: 10.1001/jamanetworkopen.2020.17357
– ident: e_1_3_4_22_2
  doi: 10.3389/fmicb.2018.00862
– ident: e_1_3_4_7_2
  doi: 10.3322/caac.21660
– ident: e_1_3_4_52_2
  doi: 10.1038/s41522-022-00279-y
– ident: e_1_3_4_54_2
  doi: 10.1080/19490976.2023.2197835
– ident: e_1_3_4_6_2
  doi: 10.1038/s41368-023-00249-w
– ident: e_1_3_4_21_2
  doi: 10.1038/s41598-017-16418-x
– ident: e_1_3_4_70_2
  doi: 10.1111/apm.13315
– ident: e_1_3_4_51_2
  doi: 10.1186/s12866-020-01801-y
– ident: e_1_3_4_23_2
  doi: 10.3389/fcimb.2021.728933
– ident: e_1_3_4_18_2
  doi: 10.3389/fmicb.2021.719601
– ident: e_1_3_4_12_2
  doi: 10.1111/jre.12691
– ident: e_1_3_4_46_2
  doi: 10.1371/journal.pcbi.1004977
– ident: e_1_3_4_63_2
  doi: 10.1016/B978-0-7020-3468-8.50201-7
– ident: e_1_3_4_11_2
  doi: 10.1128/mSystems.00323-19
– ident: e_1_3_4_26_2
  doi: 10.1186/s40168-023-01613-y
– ident: e_1_3_4_30_2
  doi: 10.1016/j.jri.2021.103293
– ident: e_1_3_4_62_2
  doi: 10.1038/s41388-021-02137-1
– ident: e_1_3_4_43_2
  doi: 10.1186/gb-2010-11-10-r106
– ident: e_1_3_4_67_2
  doi: 10.3390/ijms242015456
– ident: e_1_3_4_4_2
  doi: 10.1038/s41392-022-00974-4
– ident: e_1_3_4_57_2
  doi: 10.1177/21925682221110527
– ident: e_1_3_4_28_2
  doi: 10.1080/20002297.2022.2051352
– ident: e_1_3_4_29_2
  doi: 10.1038/s41598-020-59016-0
– ident: e_1_3_4_19_2
  doi: 10.3389/fonc.2021.737843
– ident: e_1_3_4_10_2
  doi: 10.3390/cancers15133270
– ident: e_1_3_4_37_2
  doi: 10.1038/s41587-019-0209-9
– ident: e_1_3_4_45_2
  doi: 10.5555/1953048.2078195
– ident: e_1_3_4_44_2
  doi: 10.18637/jss.v036.i03
– ident: e_1_3_4_9_2
  doi: 10.1111/jop.13546
– ident: e_1_3_4_31_2
  doi: 10.18632/aging.103108
– ident: e_1_3_4_3_2
  doi: 10.1038/s41579-023-00963-6
– ident: e_1_3_4_32_2
  doi: 10.1128/mSystems.00630-19
– ident: e_1_3_4_55_2
  doi: 10.1038/s41591-019-0406-6
– ident: e_1_3_4_71_2
  doi: 10.1128/msystems.00738-22
– ident: e_1_3_4_36_2
  doi: 10.1177/0022034520968750
– ident: e_1_3_4_60_2
  doi: 10.1038/s41598-019-46790-9
– ident: e_1_3_4_13_2
  doi: 10.1002/ijc.34460
– ident: e_1_3_4_2_2
  doi: 10.1101/gr.276482.121
– ident: e_1_3_4_40_2
  doi: 10.1038/s41467-022-33071-9
– ident: e_1_3_4_35_2
  doi: 10.3389/fcimb.2022.942328
– ident: e_1_3_4_24_2
  doi: 10.1128/spectrum.02737-22
– ident: e_1_3_4_8_2
  doi: 10.1016/j.ctarc.2024.100831
– ident: e_1_3_4_58_2
  doi: 10.1007/s42770-022-00721-5
– ident: e_1_3_4_66_2
  doi: 10.1111/jop.13492
– ident: e_1_3_4_50_2
  doi: 10.1007/s00784-020-03592-y
– ident: e_1_3_4_34_2
  doi: 10.1002/advs.201902054
– ident: e_1_3_4_33_2
  doi: 10.1016/j.isci.2022.105839
– ident: e_1_3_4_53_2
  doi: 10.1128/mBio.03281-20
– ident: e_1_3_4_48_2
  doi: 10.1038/s41598-019-52445-6
– ident: e_1_3_4_14_2
  doi: 10.1007/s00253-022-11980-5
– ident: e_1_3_4_15_2
  doi: 10.3389/fcimb.2021.663068
– ident: e_1_3_4_17_2
  doi: 10.1016/j.bbapap.2021.140659
– ident: e_1_3_4_68_2
  doi: 10.3389/fmicb.2022.968304
– ident: e_1_3_4_59_2
  doi: 10.1111/odi.12341
– ident: e_1_3_4_27_2
  doi: 10.1111/prd.12366
– volume: 12
  year: 2016
  ident: B45
  article-title: Machine learning meta-analysis of large metagenomic datasets: tools and biological insights
  publication-title: PLoS Comput Biol
  doi: 10.1371/journal.pcbi.1004977
– volume: 23
  year: 2023
  ident: B24
  article-title: Compositional and functional changes in the salivary microbiota related to oral leukoplakia and oral squamous cell carcinoma: a case control study
  publication-title: BMC Oral Health
  doi: 10.1186/s12903-023-03760-y
– volume: 7
  start-page: 16540
  year: 2017
  ident: B20
  article-title: Bacterial alterations in salivary microbiota and their association in oral cancer
  publication-title: Sci Rep
  doi: 10.1038/s41598-017-16418-x
– volume: 22
  start-page: 89
  year: 2024
  end-page: 104
  ident: B2
  article-title: The oral microbiome: diversity, biogeography and human health
  publication-title: Nat Rev Microbiol
  doi: 10.1038/s41579-023-00963-6
– volume: 26
  year: 2023
  ident: B32
  article-title: Sex differences in the oral microbiome, host traits, and their causal relationships
  publication-title: i Sci
  doi: 10.1016/j.isci.2022.105839
– volume: 4
  start-page: 255
  year: 2018
  end-page: 262
  ident: B19
  article-title: Microbial and inflammatory-based salivary biomarkers of head and neck squamous cell carcinoma
  publication-title: Clin Exp Dent Res
  doi: 10.1002/cre2.139
– volume: 10
  start-page: 2133
  year: 2020
  ident: B28
  article-title: Patterns of oral microbiota diversity in adults and children: a crowdsourced population study
  publication-title: Sci Rep
  doi: 10.1038/s41598-020-59016-0
– volume: 36
  start-page: 1
  year: 2010
  end-page: 48
  ident: B43
  article-title: Conducting meta-analyses in R with the metafor package
  publication-title: J Stat Softw
  doi: 10.18637/jss.v036.i03
– volume: 11
  start-page: 1
  year: 2010
  end-page: 12
  ident: B42
  article-title: Differential expression analysis for sequence count data
  publication-title: Genome Biol
  doi: 10.1186/gb-2010-11-10-r106
– volume: 8
  start-page: 110931
  year: 2017
  end-page: 110948
  ident: B60
  article-title: High-resolution microbiome profiling uncovers Fusobacterium nucleatum, Lactobacillus gasseri/johnsonii, and Lactobacillus vaginalis associated to oral and oropharyngeal cancer in saliva from HPV positive and HPV negative patients treated with surgery and chemo-radiation
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.20677
– volume: 15
  start-page: 1
  year: 2023
  end-page: 24
  ident: B9
  article-title: Early diagnosis of oral cancer: a complex polyhedral problem with a difficult solution
  publication-title: Cancers (Basel)
  doi: 10.3390/cancers15133270
– volume: 3
  year: 2020
  ident: B46
  article-title: Association of sleep electroencephalography-based brain age index with dementia
  publication-title: JAMA Netw Open
  doi: 10.1001/jamanetworkopen.2020.17357
– volume: 13
  start-page: 968304
  year: 2022
  ident: B67
  article-title: Systematic review and meta-analysis of oral squamous cell carcinoma associated oral microbiome
  publication-title: Front Microbiol
  doi: 10.3389/fmicb.2022.968304
– volume: 53
  start-page: 991
  year: 2022
  end-page: 1000
  ident: B57
  article-title: Effect of electronic cigarette and tobacco smoking on the human saliva microbial community
  publication-title: Braz J Microbiol
  doi: 10.1007/s42770-022-00721-5
– volume: 7
  start-page: 1
  year: 2022
  end-page: 28
  ident: B3
  article-title: Microbiota in health and diseases
  publication-title: Sig Transduct Target Ther
  doi: 10.1038/s41392-022-00974-4
– volume: 4
  start-page: 358
  year: 2018
  end-page: 365
  ident: B64
  article-title: Association of oral microbiome with risk for incident head and neck squamous cell cancer
  publication-title: JAMA Oncol
  doi: 10.1001/jamaoncol.2017.4777
– volume: 40
  start-page: 100831
  year: 2024
  ident: B7
  article-title: Factors associated with delay in diagnosis of oral cancers
  publication-title: Cancer Treat Res Commun
  doi: 10.1016/j.ctarc.2024.100831
– volume: 14
  start-page: 2051352
  year: 2022
  ident: B27
  article-title: Maturation of the oral microbiota during primary teeth eruption: a longitudinal, preliminary study
  publication-title: J Oral Microbiol
  doi: 10.1080/20002297.2022.2051352
– volume: 12
  start-page: 1624
  year: 2022
  end-page: 1626
  ident: B56
  article-title: Fixed-effect vs random-effects models for meta-analysis: 3 points to consider
  publication-title: Global Spine J
  doi: 10.1177/21925682221110527
– volume: 21
  start-page: 748
  year: 2015
  end-page: 754
  ident: B58
  article-title: Acetaldehyde production by major oral microbes
  publication-title: Oral Dis
  doi: 10.1111/odi.12341
– volume: 152
  start-page: 1903
  year: 2023
  end-page: 1915
  ident: B12
  article-title: Convergent dysbiosis of upper aerodigestive microbiota between patients with esophageal and oral cavity squamous cell carcinoma
  publication-title: Int J Cancer
  doi: 10.1002/ijc.34460
– volume: 26
  start-page: 265
  year: 2019
  end-page: 272
  ident: B40
  article-title: Meta-analysis reveals reproducible gut microbiome alterations in response to a high-fat diet
  publication-title: Cell Host Microbe
  doi: 10.1016/j.chom.2019.06.013
– volume: 6
  start-page: 1902054
  year: 2019
  ident: B33
  article-title: How and why men and women differ in their microbiomes: medical ecology and network analyses of the microgenderome
  publication-title: Adv Sci (Weinh)
  doi: 10.1002/advs.201902054
– volume: 15
  start-page: 44
  year: 2023
  ident: B5
  article-title: Oral squamous cell carcinomas: state of the field and emerging directions
  publication-title: Int J Oral Sci
  doi: 10.1038/s41368-023-00249-w
– volume: 10
  year: 2022
  ident: B23
  article-title: Oral bacteriome and mycobiome across stages of oral carcinogenesis
  publication-title: Microbiol Spectr
  doi: 10.1128/spectrum.02737-22
– volume: 1869
  start-page: 140659
  year: 2021
  ident: B16
  article-title: Meta-omics analysis indicates the saliva microbiome and its proteins associated with the prognosis of oral cancer patients
  publication-title: Biochim Biophysica Acta (BBA) Proteins Proteom
  doi: 10.1016/j.bbapap.2021.140659
– volume: 12
  start-page: 2825
  year: 2011
  end-page: 2830
  ident: B44
  article-title: Scikit-learn: machine learning in Python
  publication-title: J Mach Learn Res
  doi: 10.5555/1953048.2078195
– volume: 53
  start-page: 358
  year: 2024
  end-page: 365
  ident: B8
  article-title: The association between referral by specialists in oral diagnosis on survival rates of patients with oral cancer: a retrospective cohort study
  publication-title: J Oral Pathol Med
  doi: 10.1111/jop.13546
– volume: 41
  start-page: 1269
  year: 2022
  end-page: 1280
  ident: B61
  article-title: A dysbiotic microbiome promotes head and neck squamous cell carcinoma
  publication-title: Oncogene
  doi: 10.1038/s41388-021-02137-1
– volume: 9
  start-page: 1
  year: 2019
  end-page: 7
  ident: B47
  article-title: Comparison of oral microbiome profiles in stimulated and unstimulated saliva, tongue, and mouth-rinsed water
  publication-title: Sci Rep
  doi: 10.1038/s41598-019-52445-6
– volume: 11
  start-page: 728933
  year: 2021
  ident: B22
  article-title: The clinical potential of oral microbiota as a screening tool for oral squamous cell carcinomas
  publication-title: Front Cell Infect Microbiol
  doi: 10.3389/fcimb.2021.728933
– volume: 86
  start-page: 123
  year: 2021
  end-page: 141
  ident: B26
  article-title: Acquisition and establishment of the oral microbiota
  publication-title: Periodontol 2000
  doi: 10.1111/prd.12366
– volume: 12
  start-page: 7874
  year: 2020
  end-page: 7907
  ident: B30
  article-title: Microbiome succession with increasing age in three oral sites
  publication-title: Aging (Milano)
  doi: 10.18632/aging.103108
– volume: 25
  start-page: 679
  year: 2019
  end-page: 689
  ident: B54
  article-title: Meta-analysis of fecal metagenomes reveals global microbial signatures that are specific for colorectal cancer
  publication-title: Nat Med
  doi: 10.1038/s41591-019-0406-6
– volume: 70
  start-page: 1
  year: 2021
  end-page: 11
  ident: B15
  article-title: Identification & correlation of bacterial diversity in oral cancer and long-term tobacco chewers- a case-control pilot study
  publication-title: J Med Microbiol
  doi: 10.1099/jmm.0.001417
– volume: 71
  start-page: 209
  year: 2021
  end-page: 249
  ident: B6
  article-title: Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries
  publication-title: CA A Cancer J Clinicians
  doi: 10.3322/caac.21660
– volume: 82
  start-page: 1030
  year: 2021
  end-page: 1046
  ident: B63
  article-title: Oral microbial species and virulence factors associated with oral squamous cell carcinoma
  publication-title: Microb Ecol
  doi: 10.1007/s00248-020-01596-5
– volume: 55
  start-page: 13
  year: 2020
  end-page: 22
  ident: B11
  article-title: Role of Porphyromonas gingivalis in oral squamous cell carcinoma development: a systematic review
  publication-title: J Periodont Res
  doi: 10.1111/jre.12691
– volume: 15
  start-page: 2197835
  year: 2023
  ident: B53
  article-title: Meta-analysis reveals Helicobacter pylori mutual exclusivity and reproducible gastric microbiome alterations during gastric carcinoma progression
  publication-title: Gut Microbes
  doi: 10.1080/19490976.2023.2197835
– volume: 131
  start-page: 262
  year: 2023
  end-page: 276
  ident: B69
  article-title: Limitations of using 16S rRNA microbiome sequencing to predict oral squamous cell carcinoma
  publication-title: APMIS
  doi: 10.1111/apm.13315
– volume: 145
  start-page: 103293
  year: 2021
  ident: B29
  article-title: Oral microbiome and pregnancy: a bidirectional relationship
  publication-title: J Reprod Immunol
  doi: 10.1016/j.jri.2021.103293
– volume: 11
  start-page: 171
  year: 2023
  ident: B25
  article-title: Salivary microbiome profiles of oral cancer patients analyzed before and after treatment
  publication-title: Microbiome
  doi: 10.1186/s40168-023-01613-y
– volume: 9
  year: 2023
  ident: B68
  article-title: Microbial dysbiosis in oral squamous cell carcinoma: a systematic review and meta-analysis
  publication-title: Heliyon
  doi: 10.1016/j.heliyon.2023.e13198
– volume: 32
  start-page: 1112
  year: 2022
  end-page: 1123
  ident: B1
  article-title: Diurnal and eating-associated microbial patterns revealed via high-frequency saliva sampling
  publication-title: Genome Res
  doi: 10.1101/gr.276482.121
– volume: 4
  year: 2019
  ident: B10
  article-title: The oral mouse microbiome promotes tumorigenesis in oral squamous cell carcinoma
  publication-title: mSystems
  doi: 10.1128/mSystems.00323-19
– volume: 13
  year: 2018
  ident: B48
  article-title: Comparison of the oral microbiome in mouthwash and whole saliva samples
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0194729
– volume: 12
  year: 2021
  ident: B52
  article-title: Longitudinal multi-omics and microbiome meta-analysis identify an asymptomatic gingival state that links gingivitis, periodontitis, and aging
  publication-title: mBio
  doi: 10.1128/mBio.03281-20
– volume: 37
  start-page: 852
  year: 2019
  end-page: 857
  ident: B36
  article-title: Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2
  publication-title: Nat Biotechnol
  doi: 10.1038/s41587-019-0209-9
– volume: 25
  start-page: 2779
  year: 2021
  end-page: 2789
  ident: B49
  article-title: Comparative evaluation of microbial profiles of oral samples obtained at different collection time points and using different methods
  publication-title: Clin Oral Investig
  doi: 10.1007/s00784-020-03592-y
– volume: 2
  year: 2017
  ident: B37
  article-title: Deblur rapidly resolves single-nucleotide community sequence patterns
  publication-title: mSystems
  doi: 10.1128/mSystems.00191-16
– volume: 25
  start-page: 667
  year: 2019
  end-page: 678
  ident: B55
  article-title: Metagenomic analysis of colorectal cancer datasets identifies cross-cohort microbial diagnostic signatures and a link with choline degradation
  publication-title: Nat Med
  doi: 10.1038/s41591-019-0405-7
– volume: 106
  start-page: 4115
  year: 2022
  end-page: 4128
  ident: B13
  article-title: Comparative and analytical characterization of the oral bacteriome of smokeless tobacco users with oral squamous cell carcinoma
  publication-title: Appl Microbiol Biotechnol
  doi: 10.1007/s00253-022-11980-5
– volume: 20
  year: 2020
  ident: B50
  article-title: Defining the oral microbiome by whole-genome sequencing and resistome analysis: the complexity of the healthy picture
  publication-title: BMC Microbiol
  doi: 10.1186/s12866-020-01801-y
– start-page: 977
  year: 2008
  end-page: 979
  ident: B62
  article-title: Anaerobic Gram-positive, nonsporulating bacilli (including actinomycosis)
  publication-title: Principles and practice of pediatric infectious disease ;3rd ed ;p In ;W.B. Saunders ;Edinburgh, Scotland
– volume: 12
  start-page: 942328
  year: 2022
  ident: B34
  article-title: The oral cancer microbiome contains tumor space-specific and clinicopathology-specific bacteria
  publication-title: Front Cell Infect Microbiol
  doi: 10.3389/fcimb.2022.942328
– volume: 11
  start-page: 737843
  year: 2021
  ident: B18
  article-title: Restoration of the oral microbiota after surgery for head and neck squamous cell carcinoma is associated with patient outcomes
  publication-title: Front Oncol
  doi: 10.3389/fonc.2021.737843
– volume: 5
  year: 2020
  ident: B31
  article-title: Human skin, oral, and gut microbiomes predict chronological age
  publication-title: mSystems
  doi: 10.1128/mSystems.00630-19
– volume: 13
  start-page: 895537
  year: 2022
  end-page: 895555
  ident: B4
  article-title: The oral microbiota: community composition, influencing factors, pathogenesis, and interventions
  publication-title: Front Microbiol
  doi: 10.3389/fmicb.2022.895537
– volume: 72
  start-page: 5069
  year: 2006
  end-page: 5072
  ident: B38
  article-title: Greengenes, a chimera-checked 16S rRNA gene database and workbench compatible with ARB
  publication-title: Appl Environ Microbiol
  doi: 10.1128/AEM.03006-05
– volume: 13
  start-page: 1
  year: 2022
  end-page: 14
  ident: B39
  article-title: Batch effects removal for microbiome data via conditional quantile regression
  publication-title: Nat Commun
  doi: 10.1038/s41467-022-33071-9
– volume: 8
  year: 2023
  ident: B70
  article-title: Systematic evaluation of the viable microbiome in the human oral and gut samples with spike-in Gram+/- bacteria
  publication-title: mSystems
  doi: 10.1128/msystems.00738-22
– volume: 52
  start-page: 911
  year: 2023
  end-page: 918
  ident: B65
  article-title: Oral microbiome characterization in oral mucositis patients—a systematic review
  publication-title: J Oral Pathology Medicine
  doi: 10.1111/jop.13492
– volume: 12
  start-page: 719601
  year: 2021
  ident: B17
  article-title: Oral microbiota analysis of tissue pairs and saliva samples from patients with oral squamous cell carcinoma - a pilot study
  publication-title: Front Microbiol
  doi: 10.3389/fmicb.2021.719601
– volume: 67
  start-page: 882
  year: 2018
  end-page: 891
  ident: B41
  article-title: Leveraging sequence-based faecal microbial community survey data to identify a composite biomarker for colorectal cancer
  publication-title: Gut
  doi: 10.1136/gutjnl-2016-313189
– volume: 24
  start-page: 1
  year: 2023
  end-page: 15
  ident: B66
  article-title: Potential role of the intratumoral microbiota in prognosis of head and neck cancer
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms242015456
– volume: 9
  start-page: 10446
  year: 2019
  ident: B59
  article-title: Metabolic property of acetaldehyde production from ethanol and glucose by oral Streptococcus and Neisseria
  publication-title: Sci Rep
  doi: 10.1038/s41598-019-46790-9
– volume: 11
  start-page: 663068
  year: 2021
  ident: B14
  article-title: Taxonomic and functional dysregulation in salivary microbiomes during oral carcinogenesis
  publication-title: Front Cell Infect Microbiol
  doi: 10.3389/fcimb.2021.663068
– volume: 8
  start-page: 38
  year: 2022
  ident: B51
  article-title: Citizen-science reveals changes in the oral microbiome in Spain through age and lifestyle factors
  publication-title: NPJ Biofilms Microbiomes
  doi: 10.1038/s41522-022-00279-y
– volume: 9
  start-page: 862
  year: 2018
  ident: B21
  article-title: Oral microbiota community dynamics associated with oral squamous cell carcinoma staging
  publication-title: Front Microbiol
  doi: 10.3389/fmicb.2018.00862
– volume: 100
  start-page: 397
  year: 2021
  end-page: 405
  ident: B35
  article-title: Carcinogenesis of male oral submucous fibrosis alters salivary microbiomes
  publication-title: J Dent Res
  doi: 10.1177/0022034520968750
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SecondaryResourceType review_article
Snippet The oral cavity hosts a diverse microbial community that plays a crucial role in systemic and oral health. Accumulated research has investigated significant...
Oral squamous cell carcinoma (OSCC) is a prevalent malignancy in the oral-maxillofacial region with a poor prognosis. Oral microbiomes play a potential role in...
ABSTRACTOral squamous cell carcinoma (OSCC) is a prevalent malignancy in the oral-maxillofacial region with a poor prognosis. Oral microbiomes play a potential...
ABSTRACT Oral squamous cell carcinoma (OSCC) is a prevalent malignancy in the oral-maxillofacial region with a poor prognosis. Oral microbiomes play a...
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StartPage e0124724
SubjectTerms age
Biomarkers
Cancer
Carcinoma, Squamous Cell - microbiology
Clinical Microbiology
Dysbacteriosis
Dysbiosis - microbiology
Female
Gender
Host Microbial Interactions
Humans
Invasiveness
Learning algorithms
Machine learning
Male
Malignancy
Maxillofacial
Meta-analysis
Microbiomes
Microbiota
Microorganisms
Mouth Neoplasms - microbiology
Oral carcinoma
Oral cavity
Oral squamous cell carcinoma
Pathogenesis
Research Article
Saliva
Saliva - microbiology
salivary microbiome
Squamous cell carcinoma
Squamous Cell Carcinoma of Head and Neck - microbiology
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Title Systematic analyses uncover robust salivary microbial signatures and host-microbiome perturbations in oral squamous cell carcinoma
URI https://www.ncbi.nlm.nih.gov/pubmed/39873508
https://journals.asm.org/doi/10.1128/msystems.01247-24
https://www.proquest.com/docview/3203849855
https://www.proquest.com/docview/3160461603
https://pubmed.ncbi.nlm.nih.gov/PMC11834404
https://doaj.org/article/5f70153840c74f94b2eb6777bfea49f2
Volume 10
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