Composition of subgingival microbiota associated with periodontitis and diagnosis of malignancy—a cross-sectional study

Periodontitis is one of the world’s most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and ti...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in microbiology Vol. 14; p. 1172340
Main Authors Narayanan, Aswathy, Söder, Birgitta, Meurman, Jukka, Lundmark, Anna, Hu, Yue O. O., Neogi, Ujjwal, Yucel-Lindberg, Tülay
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 2023
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Periodontitis is one of the world’s most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and tissue destruction. Chronic systemic low-grade inflammation is involved in numerous diseases, and it is also known that long-lasting inflammation and chronic infections predispose one to cancer. Here, we characterized and compared the subgingival microbiota associated with periodontitis and diagnosis of malignancy in a longitudinal 10-year follow-up study. The study was conducted on 50 patients with periodontitis and 40 periodontally healthy individuals. The recorded clinical oral health parameters were periodontal attachment loss (AL), bleeding on probing (BOP), gingival index (GI), probing depth (PD), and plaque index (PI). Subgingival plaque was collected from each participant, from which DNA was extracted, and 16S rRNA gene amplicon sequencing performed. Cancer diagnoses data were collected between the years 2008–2018 from the Swedish Cancer Registry. The participants were categorized based on having cancer at the time of sample collection (CSC), having developed cancer later (DCL), and controls without any cancer. The most abundant phyla across all 90 samples were Actinobacteria , Proteobacteria , Firmicutes , Bacteroidetes , and Fusobacteria . At the genus level, Treponema , Fretibacterium , and Prevotella were significantly more abundant in samples of periodontitis patients compared to non-periodontitis individuals. With regard to samples of cancer patients, Corynebacterium and Streptococcus were more abundant in the CSC group; Prevotella were more abundant in the DCL group; and Rothia , Neisseria , and Capnocytophaga were more abundant in the control group. In the CSC group, we also found that the presence of periodontal inflammation, in terms of BOP, GI, and PLI, significantly correlated with species belonging to the genera Prevotella , Treponema , and Mycoplasma . Our results revealed that several subgingival genera were differentially enriched among the studied groups. These findings underscore the need for further research to fully understand the role that oral pathogens may play in the development of cancer.
AbstractList Periodontitis is one of the world's most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and tissue destruction. Chronic systemic low-grade inflammation is involved in numerous diseases, and it is also known that long-lasting inflammation and chronic infections predispose one to cancer. Here, we characterized and compared the subgingival microbiota associated with periodontitis and diagnosis of malignancy in a longitudinal 10-year follow-up study. The study was conducted on 50 patients with periodontitis and 40 periodontally healthy individuals. The recorded clinical oral health parameters were periodontal attachment loss (AL), bleeding on probing (BOP), gingival index (GI), probing depth (PD), and plaque index (PI). Subgingival plaque was collected from each participant, from which DNA was extracted, and 16S rRNA gene amplicon sequencing performed. Cancer diagnoses data were collected between the years 2008-2018 from the Swedish Cancer Registry. The participants were categorized based on having cancer at the time of sample collection (CSC), having developed cancer later (DCL), and controls without any cancer. The most abundant phyla across all 90 samples were , , , , and . At the genus level, , , and were significantly more abundant in samples of periodontitis patients compared to non-periodontitis individuals. With regard to samples of cancer patients, and were more abundant in the CSC group; were more abundant in the DCL group; and , , and were more abundant in the control group. In the CSC group, we also found that the presence of periodontal inflammation, in terms of BOP, GI, and PLI, significantly correlated with species belonging to the genera , , and . Our results revealed that several subgingival genera were differentially enriched among the studied groups. These findings underscore the need for further research to fully understand the role that oral pathogens may play in the development of cancer.
Periodontitis is one of the world’s most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and tissue destruction. Chronic systemic low-grade inflammation is involved in numerous diseases, and it is also known that long-lasting inflammation and chronic infections predispose one to cancer. Here, we characterized and compared the subgingival microbiota associated with periodontitis and diagnosis of malignancy in a longitudinal 10-year follow-up study. The study was conducted on 50 patients with periodontitis and 40 periodontally healthy individuals. The recorded clinical oral health parameters were periodontal attachment loss (AL), bleeding on probing (BOP), gingival index (GI), probing depth (PD), and plaque index (PI). Subgingival plaque was collected from each participant, from which DNA was extracted, and 16S rRNA gene amplicon sequencing performed. Cancer diagnoses data were collected between the years 2008–2018 from the Swedish Cancer Registry. The participants were categorized based on having cancer at the time of sample collection (CSC), having developed cancer later (DCL), and controls without any cancer. The most abundant phyla across all 90 samples were Actinobacteria, Proteobacteria, Firmicutes, Bacteroidetes, and Fusobacteria. At the genus level, Treponema, Fretibacterium, and Prevotella were significantly more abundant in samples of periodontitis patients compared to non-periodontitis individuals. With regard to samples of cancer patients, Corynebacterium and Streptococcus were more abundant in the CSC group; Prevotella were more abundant in the DCL group; and Rothia, Neisseria, and Capnocytophaga were more abundant in the control group. In the CSC group, we also found that the presence of periodontal inflammation, in terms of BOP, GI, and PLI, significantly correlated with species belonging to the genera Prevotella, Treponema, and Mycoplasma. Our results revealed that several subgingival genera were differentially enriched among the studied groups. These findings underscore the need for further research to fully understand the role that oral pathogens may play in the development of cancer.
Periodontitis is one of the world’s most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and tissue destruction. Chronic systemic low-grade inflammation is involved in numerous diseases, and it is also known that long-lasting inflammation and chronic infections predispose one to cancer. Here, we characterized and compared the subgingival microbiota associated with periodontitis and diagnosis of malignancy in a longitudinal 10-year follow-up study. The study was conducted on 50 patients with periodontitis and 40 periodontally healthy individuals. The recorded clinical oral health parameters were periodontal attachment loss (AL), bleeding on probing (BOP), gingival index (GI), probing depth (PD), and plaque index (PI). Subgingival plaque was collected from each participant, from which DNA was extracted, and 16S rRNA gene amplicon sequencing performed. Cancer diagnoses data were collected between the years 2008–2018 from the Swedish Cancer Registry. The participants were categorized based on having cancer at the time of sample collection (CSC), having developed cancer later (DCL), and controls without any cancer. The most abundant phyla across all 90 samples were Actinobacteria , Proteobacteria , Firmicutes , Bacteroidetes , and Fusobacteria . At the genus level, Treponema , Fretibacterium , and Prevotella were significantly more abundant in samples of periodontitis patients compared to non-periodontitis individuals. With regard to samples of cancer patients, Corynebacterium and Streptococcus were more abundant in the CSC group; Prevotella were more abundant in the DCL group; and Rothia , Neisseria , and Capnocytophaga were more abundant in the control group. In the CSC group, we also found that the presence of periodontal inflammation, in terms of BOP, GI, and PLI, significantly correlated with species belonging to the genera Prevotella , Treponema , and Mycoplasma . Our results revealed that several subgingival genera were differentially enriched among the studied groups. These findings underscore the need for further research to fully understand the role that oral pathogens may play in the development of cancer.
Periodontitis is one of the world's most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and tissue destruction. Chronic systemic low-grade inflammation is involved in numerous diseases, and it is also known that long-lasting inflammation and chronic infections predispose one to cancer. Here, we characterized and compared the subgingival microbiota associated with periodontitis and diagnosis of malignancy in a longitudinal 10-year follow-up study. The study was conducted on 50 patients with periodontitis and 40 periodontally healthy individuals. The recorded clinical oral health parameters were periodontal attachment loss (AL), bleeding on probing (BOP), gingival index (GI), probing depth (PD), and plaque index (PI). Subgingival plaque was collected from each participant, from which DNA was extracted, and 16S rRNA gene amplicon sequencing performed. Cancer diagnoses data were collected between the years 2008-2018 from the Swedish Cancer Registry. The participants were categorized based on having cancer at the time of sample collection (CSC), having developed cancer later (DCL), and controls without any cancer. The most abundant phyla across all 90 samples were Actinobacteria, Proteobacteria, Firmicutes, Bacteroidetes, and Fusobacteria. At the genus level, Treponema, Fretibacterium, and Prevotella were significantly more abundant in samples of periodontitis patients compared to non-periodontitis individuals. With regard to samples of cancer patients, Corynebacterium and Streptococcus were more abundant in the CSC group; Prevotella were more abundant in the DCL group; and Rothia, Neisseria, and Capnocytophaga were more abundant in the control group. In the CSC group, we also found that the presence of periodontal inflammation, in terms of BOP, GI, and PLI, significantly correlated with species belonging to the genera Prevotella, Treponema, and Mycoplasma. Our results revealed that several subgingival genera were differentially enriched among the studied groups. These findings underscore the need for further research to fully understand the role that oral pathogens may play in the development of cancer.Periodontitis is one of the world's most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and tissue destruction. Chronic systemic low-grade inflammation is involved in numerous diseases, and it is also known that long-lasting inflammation and chronic infections predispose one to cancer. Here, we characterized and compared the subgingival microbiota associated with periodontitis and diagnosis of malignancy in a longitudinal 10-year follow-up study. The study was conducted on 50 patients with periodontitis and 40 periodontally healthy individuals. The recorded clinical oral health parameters were periodontal attachment loss (AL), bleeding on probing (BOP), gingival index (GI), probing depth (PD), and plaque index (PI). Subgingival plaque was collected from each participant, from which DNA was extracted, and 16S rRNA gene amplicon sequencing performed. Cancer diagnoses data were collected between the years 2008-2018 from the Swedish Cancer Registry. The participants were categorized based on having cancer at the time of sample collection (CSC), having developed cancer later (DCL), and controls without any cancer. The most abundant phyla across all 90 samples were Actinobacteria, Proteobacteria, Firmicutes, Bacteroidetes, and Fusobacteria. At the genus level, Treponema, Fretibacterium, and Prevotella were significantly more abundant in samples of periodontitis patients compared to non-periodontitis individuals. With regard to samples of cancer patients, Corynebacterium and Streptococcus were more abundant in the CSC group; Prevotella were more abundant in the DCL group; and Rothia, Neisseria, and Capnocytophaga were more abundant in the control group. In the CSC group, we also found that the presence of periodontal inflammation, in terms of BOP, GI, and PLI, significantly correlated with species belonging to the genera Prevotella, Treponema, and Mycoplasma. Our results revealed that several subgingival genera were differentially enriched among the studied groups. These findings underscore the need for further research to fully understand the role that oral pathogens may play in the development of cancer.
Author Lundmark, Anna
Hu, Yue O. O.
Neogi, Ujjwal
Yucel-Lindberg, Tülay
Narayanan, Aswathy
Meurman, Jukka
Söder, Birgitta
AuthorAffiliation 3 Division of Periodontology, Department of Dental Medicine, Karolinska Institutet , Huddinge , Sweden
2 Division of Infectious Diseases, Department of Medicine Huddinge, Karolinska Institutet , Stockholm , Sweden
6 Department of Microbiology, Tumor and Cell Biology, Centre for Translational Microbiome Research, Karolinska Institutet , Stockholm , Sweden
1 Division of Clinical Microbiology, Department of Laboratory Medicine, ANA Futura, Karolinska Institutet , Stockholm , Sweden
8 The Systems Virology Lab, Division of Clinical Microbiology, Department of Laboratory Medicine, ANA Futura, Karolinska Institutet , Stockholm , Sweden
7 School of Environmental Science and Engineering, Hubei Polytechnic University , Huangshi , China
4 Department of Oral and Maxillofacial Diseases, University of Helsinki and Helsinki University Hospital , Helsinki , Finland
5 Division of Pediatric Dentistry, Department of Dental Medicine, Karolinska Institutet , Huddinge , Sweden
AuthorAffiliation_xml – name: 2 Division of Infectious Diseases, Department of Medicine Huddinge, Karolinska Institutet , Stockholm , Sweden
– name: 4 Department of Oral and Maxillofacial Diseases, University of Helsinki and Helsinki University Hospital , Helsinki , Finland
– name: 5 Division of Pediatric Dentistry, Department of Dental Medicine, Karolinska Institutet , Huddinge , Sweden
– name: 1 Division of Clinical Microbiology, Department of Laboratory Medicine, ANA Futura, Karolinska Institutet , Stockholm , Sweden
– name: 6 Department of Microbiology, Tumor and Cell Biology, Centre for Translational Microbiome Research, Karolinska Institutet , Stockholm , Sweden
– name: 7 School of Environmental Science and Engineering, Hubei Polytechnic University , Huangshi , China
– name: 3 Division of Periodontology, Department of Dental Medicine, Karolinska Institutet , Huddinge , Sweden
– name: 8 The Systems Virology Lab, Division of Clinical Microbiology, Department of Laboratory Medicine, ANA Futura, Karolinska Institutet , Stockholm , Sweden
Author_xml – sequence: 1
  givenname: Aswathy
  surname: Narayanan
  fullname: Narayanan, Aswathy
– sequence: 2
  givenname: Birgitta
  surname: Söder
  fullname: Söder, Birgitta
– sequence: 3
  givenname: Jukka
  surname: Meurman
  fullname: Meurman, Jukka
– sequence: 4
  givenname: Anna
  surname: Lundmark
  fullname: Lundmark, Anna
– sequence: 5
  givenname: Yue O. O.
  surname: Hu
  fullname: Hu, Yue O. O.
– sequence: 6
  givenname: Ujjwal
  surname: Neogi
  fullname: Neogi, Ujjwal
– sequence: 7
  givenname: Tülay
  surname: Yucel-Lindberg
  fullname: Yucel-Lindberg, Tülay
BackLink https://www.ncbi.nlm.nih.gov/pubmed/37426027$$D View this record in MEDLINE/PubMed
BookMark eNp9ks1u1DAUhSNUREvpC7BAWbKZwbHjn6wQGkGpVIkNSOys67_UVWIPsVM0Ox6CJ-RJ6sxMUcsCL2zLvuc78vV5WZ2EGGxVvW7QmhDRvXOj12qNESbrpuGYtOhZddYw1q4Iwt9PHu1Pq4uUblEZLcJlflGdEt5ihjA_q3abOG5j8tnHUEdXp1n1PvT-Doa6OExR-ZihhpSi9pCtqX_6fFNv7eSjiSEXYaohmNp46EMBpYUywuD7AEHv_vz6DXXBpLRKVi8uBZzybHavqucOhmQvjut59e3Tx6-bz6vrL5dXmw_XK00RzyvONOpEeQdzTHVMEQdcKKaAUks57bizlomWtZgwQSkyHReEGIY67IwjgpxXVweuiXArt5MfYdrJCF7uD-LUS5iy14OV3GLsGtYiLnjLDFXKNQXTKMysgpYW1vsDazur0RptQ55geAJ9ehP8jezjnWwQwZSLhfD2SJjij9mmLEeftB0GCDbOSWJBOkxxqS6lbx6b_XV5-LxSIA4F-_5O1kntMyw9Lt5-KKZyiYrcR0UuUZHHqBQp_kf6QP-P6B5AkMX-
CitedBy_id crossref_primary_10_1007_s00784_025_06267_8
crossref_primary_10_1038_s41598_023_50410_y
crossref_primary_10_1080_20002297_2024_2391640
crossref_primary_10_3390_ijms25179374
crossref_primary_10_3390_jcm13133756
Cites_doi 10.18632/oncotarget.4209
10.1111/j.1600-0757.1997.tb00189.x
10.1111/j.1600-0765.2006.00957.x
10.1155/2012/821383
10.1038/ismej.2010.30
10.1111/j.1600-051X.2011.01813.x
10.1038/s41598-017-11779-9
10.1128/JCM.43.11.5721-5732.2005
10.1016/j.cyto.2015.02.001
10.1017/erm.2013.8
10.1186/gb-2012-13-6-r42
10.1158/1055-9965.EPI-17-0212
10.1016/j.imbio.2011.05.005
10.1186/gb-2011-12-6-r60
10.1089/cmb.2017.0096
10.1177/0022034514542468
10.1007/s10549-010-1221-4
10.1016/j.ajpath.2010.12.048
10.3389/fimmu.2020.591088
10.1146/annurev.micro.54.1.49
10.1007/s10552-011-9892-7
10.1111/prd.12425
10.3389/fcimb.2021.766944
10.7150/jca.7402
10.1371/journal.pone.0182992
10.1093/epirev/mxx006
10.1038/s41587-019-0209-9
10.3389/fonc.2022.901098
10.1111/j.1525-1470.1990.tb01035.x
10.1038/ismej.2011.191
10.1016/j.jdent.2009.05.013
10.1101/gr.126573.111
10.3389/fmicb.2017.01937
10.3389/fcimb.2019.00216
10.3233/TUB-200066
10.1016/j.it.2013.09.001
10.1038/ismej.2011.41
10.3389/fmicb.2022.895537
10.1902/jop.2015.140520
10.1038/s41577-020-00488-6
10.1186/1756-9966-30-11
10.3389/fcimb.2022.864479
10.1111/jcpe.13402
10.21147/j.issn.1000-9604.2020.06.07
10.3389/fcimb.2021.663756
10.1016/j.micpath.2019.04.034
10.1177/154405910808701104
10.1038/nature01322
10.1126/science.aaa4972
10.1002/9781118445112.stat07841
10.1016/S1470-2045(12)70137-7
10.1093/carcin/bgt249
10.1111/j.1442-2050.2012.01328.x
10.1371/journal.pone.0010029
10.1111/j.1600-0757.2011.00413.x
10.1073/pnas.1905238116
10.1038/nri3785
10.1001/jamaoncol.2017.4777
10.1136/gutjnl-2017-314814
10.1111/iej.13893
10.1038/nature13479
10.1177/0022034520952401
10.1016/j.cyto.2011.12.008
10.1902/jop.2007.060264
10.1128/AEM.00462-17
10.1111/j.1600-0757.1999.tb00158.x
10.3389/froh.2021.722495
10.3389/fmicb.2018.01603
ContentType Journal Article
Copyright Copyright © 2023 Narayanan, Söder, Meurman, Lundmark, Hu, Neogi and Yucel-Lindberg.
Copyright © 2023 Narayanan, Söder, Meurman, Lundmark, Hu, Neogi and Yucel-Lindberg. 2023 Narayanan, Söder, Meurman, Lundmark, Hu, Neogi and Yucel-Lindberg
Copyright_xml – notice: Copyright © 2023 Narayanan, Söder, Meurman, Lundmark, Hu, Neogi and Yucel-Lindberg.
– notice: Copyright © 2023 Narayanan, Söder, Meurman, Lundmark, Hu, Neogi and Yucel-Lindberg. 2023 Narayanan, Söder, Meurman, Lundmark, Hu, Neogi and Yucel-Lindberg
DBID AAYXX
CITATION
NPM
7X8
5PM
DOA
DOI 10.3389/fmicb.2023.1172340
DatabaseName CrossRef
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
Directory of Open Access Journals - May need to register for free articles
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList PubMed


CrossRef
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Biology
EISSN 1664-302X
ExternalDocumentID oai_doaj_org_article_7e22f164078746d5bbf192f1b26eba45
PMC10325785
37426027
10_3389_fmicb_2023_1172340
Genre Journal Article
GrantInformation_xml – fundername: ;
  grantid: Grant Nos 2018-06156 and 2021-01756
– fundername: National Board of Health and Welfare and Science for Life Laboratory, the National Genomics Infrastructure, NGI, and Uppmax
– fundername: ;
  grantid: Grant No. 2017-02084
– fundername: Swedish National Infrastructure for Computing (SNIC) at [SNIC CENTRE]
  grantid: 2018-05973
GroupedDBID 53G
5VS
9T4
AAFWJ
AAKDD
AAYXX
ACGFO
ACGFS
ACXDI
ADBBV
ADRAZ
AENEX
AFPKN
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BAWUL
BCNDV
CITATION
DIK
ECGQY
GROUPED_DOAJ
GX1
HYE
KQ8
M48
M~E
O5R
O5S
OK1
PGMZT
RNS
RPM
IPNFZ
NPM
RIG
7X8
5PM
ID FETCH-LOGICAL-c507t-76c0983026f6b96b3fa78b6ba55e57597fee684642368550d97833d6092fdf383
IEDL.DBID M48
ISSN 1664-302X
IngestDate Wed Aug 27 01:28:46 EDT 2025
Thu Aug 21 18:37:07 EDT 2025
Fri Jul 11 11:29:44 EDT 2025
Thu Apr 03 07:03:48 EDT 2025
Tue Jul 01 00:58:15 EDT 2025
Thu Apr 24 23:03:29 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords supragingival plaque
16S rRNA gene sequencing
cancer
malignancy
oral microbiota
periodontitis
Language English
License Copyright © 2023 Narayanan, Söder, Meurman, Lundmark, Hu, Neogi and Yucel-Lindberg.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c507t-76c0983026f6b96b3fa78b6ba55e57597fee684642368550d97833d6092fdf383
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Reviewed by: Zhenting Xiang, University of Pennsylvania, United States; Peter Allan Jorth, Cedars-Sinai Medical Center, United States
These authors have contributed equally to this work
Edited by: Lihong Peng, Hunan University of Technology, China
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.3389/fmicb.2023.1172340
PMID 37426027
PQID 2839252325
PQPubID 23479
ParticipantIDs doaj_primary_oai_doaj_org_article_7e22f164078746d5bbf192f1b26eba45
pubmedcentral_primary_oai_pubmedcentral_nih_gov_10325785
proquest_miscellaneous_2839252325
pubmed_primary_37426027
crossref_citationtrail_10_3389_fmicb_2023_1172340
crossref_primary_10_3389_fmicb_2023_1172340
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2023
PublicationDateYYYYMMDD 2023-01-01
PublicationDate_xml – year: 2023
  text: 2023
PublicationDecade 2020
PublicationPlace Switzerland
PublicationPlace_xml – name: Switzerland
PublicationTitle Frontiers in microbiology
PublicationTitleAlternate Front Microbiol
PublicationYear 2023
Publisher Frontiers Media S.A
Publisher_xml – name: Frontiers Media S.A
References Abdulamir (ref2) 2011; 30
Herlemann (ref32) 2011; 5
Ahn (ref3) 2012; 23
Anderson (ref4) 2017
Soder (ref63) 2021; 43
Buyuktimkin (ref13) 2019; 132
Michaud (ref47) 2017; 39
Andrews (ref5) 2015
Hajishengallis (ref28) 2015; 15
Van Dyke (ref65) 2009; 37
Hajishengallis (ref27) 2014; 35
Soder (ref62) 2007; 42
Segata (ref60) 2011; 12
Serhan (ref61) 2014; 510
Coussens (ref16) 2002; 420
Dye (ref20) 2012; 2000
Pollanen (ref56) 2012; 2012
Dong (ref19) 2018; 9
Li (ref41) 2021; 48
Belstrøm (ref10) 2017; 12
de Martel (ref18) 2012; 13
Sedghi (ref58) 2021; 11
Yakob (ref68) 2012; 39
Kostic (ref38) 2012; 22
Virtanen (ref67) 2014; 5
Hanke (ref30) 1990; 126
Bascones (ref9) 2005; 36
Li (ref40) 2022; 13
Yucel-Lindberg (ref69) 2013; 15
Lundin (ref43) 2010; 5
Oliveira (ref50) 2017; 8
Groeger (ref26) 2011; 216
O'Toole (ref51) 2000; 54
Bai (ref8) 2022; 12
Michaud (ref46) 2013; 34
Page (ref52) 2007; 78
Romandini (ref57) 2021; 100
Lamont (ref39) 2022; 89
Page (ref53) 1997; 14
Kechin (ref35) 2017; 24
Davanian (ref17) 2012; 57
Flemer (ref22) 2018; 67
Aas (ref1) 2005; 43
Kawamoto (ref34) 2021; 2
Perez-Chaparro (ref55) 2014; 93
Lundmark (ref44) 2019; 9
Velusamy (ref66) 2019; 116
Nwizu (ref49) 2017; 26
Hayes (ref31) 2018; 4
Liu (ref42) 2020; 32
Kim (ref37) 2022; 12
Irfan (ref33) 2020; 11
Cai (ref14) 2021; 11
Eke (ref21) 2015; 86
Gallimidi (ref23) 2015; 6
Perez-Carrasco (ref54) 2023; 56
Båge (ref7) 2011; 178
Soder (ref64) 2011; 127
Bik (ref11) 2010; 4
Bolyen (ref12) 2019; 37
Cavalla (ref15) 2015; 73
Norder Grusell (ref48) 2013; 26
Griffen (ref25) 2012; 6
Keijser (ref36) 2008; 87
Segata (ref59) 2012; 13
Asikainen (ref6) 2000
Meuric (ref45) 2017; 83
Hajishengallis (ref29) 2021; 21
Zhao (ref70) 2017; 7
Garrett (ref24) 2015; 348
References_xml – volume: 6
  start-page: 22613
  year: 2015
  ident: ref23
  article-title: Periodontal pathogens Porphyromonas gingivalis and Fusobacterium nucleatum promote tumor progression in an oral-specific chemical carcinogenesis model
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.4209
– volume: 14
  start-page: 9
  year: 1997
  ident: ref53
  article-title: The pathogenesis of human periodontitis: an introduction
  publication-title: Periodontol.
  doi: 10.1111/j.1600-0757.1997.tb00189.x
– volume: 42
  start-page: 361
  year: 2007
  ident: ref62
  article-title: Periodontitis and premature death: a 16-year longitudinal study in a Swedish urban population
  publication-title: J. Periodontal Res.
  doi: 10.1111/j.1600-0765.2006.00957.x
– volume: 2012
  start-page: 821383
  year: 2012
  ident: ref56
  article-title: Host-bacteria crosstalk at the dentogingival junction
  publication-title: Int J Dent
  doi: 10.1155/2012/821383
– volume: 4
  start-page: 962
  year: 2010
  ident: ref11
  article-title: Bacterial diversity in the oral cavity of 10 healthy individuals
  publication-title: ISME J.
  doi: 10.1038/ismej.2010.30
– volume: 39
  start-page: 256
  year: 2012
  ident: ref68
  article-title: Associations of periodontal microorganisms with salivary proteins and MMP-8 in gingival crevicular fluid
  publication-title: J. Clin. Periodontol.
  doi: 10.1111/j.1600-051X.2011.01813.x
– volume: 7
  start-page: 11773
  year: 2017
  ident: ref70
  article-title: Variations in oral microbiota associated with oral cancer
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-017-11779-9
– volume: 43
  start-page: 5721
  year: 2005
  ident: ref1
  article-title: Defining the normal bacterial flora of the oral cavity
  publication-title: J. Clin. Microbiol.
  doi: 10.1128/JCM.43.11.5721-5732.2005
– volume: 73
  start-page: 114
  year: 2015
  ident: ref15
  article-title: Matrix metalloproteinases regulate extracellular levels of SDF-1/CXCL12, IL-6 and VEGF in hydrogen peroxide-stimulated human periodontal ligament fibroblasts
  publication-title: Cytokine
  doi: 10.1016/j.cyto.2015.02.001
– volume: 15
  start-page: e7
  year: 2013
  ident: ref69
  article-title: Inflammatory mediators in the pathogenesis of periodontitis
  publication-title: Expert Rev. Mol. Med.
  doi: 10.1017/erm.2013.8
– volume: 13
  start-page: R42
  year: 2012
  ident: ref59
  article-title: Composition of the adult digestive tract bacterial microbiome based on seven mouth surfaces, tonsils, throat and stool samples
  publication-title: Genome Biol.
  doi: 10.1186/gb-2012-13-6-r42
– volume: 26
  start-page: 1255
  year: 2017
  ident: ref49
  article-title: Periodontal disease and incident Cancer risk among postmenopausal women: results from the Women's Health Initiative observational cohort
  publication-title: Cancer Epidemiol. Biomark. Prev.
  doi: 10.1158/1055-9965.EPI-17-0212
– volume: 216
  start-page: 1302
  year: 2011
  ident: ref26
  article-title: B7-H1 and B7-DC receptors of oral squamous carcinoma cells are upregulated by Porphyromonas gingivalis
  publication-title: Immunobiology
  doi: 10.1016/j.imbio.2011.05.005
– volume: 12
  start-page: R60
  year: 2011
  ident: ref60
  article-title: Metagenomic biomarker discovery and explanation
  publication-title: Genome Biol.
  doi: 10.1186/gb-2011-12-6-r60
– year: 2015
  ident: ref5
  article-title: FASTQC a quality control tool for high throughput sequence data. Babraham Institute
– volume: 24
  start-page: 1138
  year: 2017
  ident: ref35
  article-title: cutPrimers: a new tool for accurate cutting of primers from reads of targeted next generation sequencing
  publication-title: J. Comput. Biol.
  doi: 10.1089/cmb.2017.0096
– volume: 93
  start-page: 846
  year: 2014
  ident: ref55
  article-title: Newly identified pathogens associated with periodontitis: a systematic review
  publication-title: J. Dent. Res.
  doi: 10.1177/0022034514542468
– volume: 127
  start-page: 497
  year: 2011
  ident: ref64
  article-title: Periodontal disease may associate with breast cancer
  publication-title: Breast Cancer Res. Treat.
  doi: 10.1007/s10549-010-1221-4
– volume: 178
  start-page: 1676
  year: 2011
  ident: ref7
  article-title: Expression of prostaglandin E synthases in periodontitis immunolocalization and cellular regulation
  publication-title: Am. J. Pathol.
  doi: 10.1016/j.ajpath.2010.12.048
– volume: 36
  start-page: 299
  year: 2005
  ident: ref9
  article-title: Tissue destruction in periodontitis: bacteria or cytokines fault?
  publication-title: Quintessence Int.
– volume: 11
  start-page: 591088
  year: 2020
  ident: ref33
  article-title: The Oral microbiome and Cancer
  publication-title: Front. Immunol.
  doi: 10.3389/fimmu.2020.591088
– volume: 54
  start-page: 49
  year: 2000
  ident: ref51
  article-title: Biofilm formation as microbial development
  publication-title: Annu. Rev. Microbiol.
  doi: 10.1146/annurev.micro.54.1.49
– volume: 23
  start-page: 399
  year: 2012
  ident: ref3
  article-title: Oral microbiome and oral and gastrointestinal cancer risk
  publication-title: Cancer Causes Control
  doi: 10.1007/s10552-011-9892-7
– volume: 89
  start-page: 154
  year: 2022
  ident: ref39
  article-title: Role of Porphyromonas gingivalis in oral and orodigestive squamous cell carcinoma
  publication-title: Periodontol.
  doi: 10.1111/prd.12425
– volume: 11
  start-page: 766944
  year: 2021
  ident: ref58
  article-title: Periodontal disease: the good, the bad, and the unknown
  publication-title: Front. Cell. Infect. Microbiol.
  doi: 10.3389/fcimb.2021.766944
– volume: 5
  start-page: 79
  year: 2014
  ident: ref67
  article-title: History of dental infections associates with cancer in periodontally healthy subjects: a 24-year follow-up study from Sweden
  publication-title: J. Cancer
  doi: 10.7150/jca.7402
– volume: 12
  start-page: e0182992
  year: 2017
  ident: ref10
  article-title: Microbial profile comparisons of saliva, pooled and site-specific subgingival samples in periodontitis patients
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0182992
– volume: 39
  start-page: 49
  year: 2017
  ident: ref47
  article-title: Periodontal disease, tooth loss, and Cancer risk
  publication-title: Epidemiol. Rev.
  doi: 10.1093/epirev/mxx006
– volume: 37
  start-page: 852
  year: 2019
  ident: ref12
  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: 12
  start-page: 901098
  year: 2022
  ident: ref37
  article-title: Periodontal disease and cancer risk: a nationwide population-based cohort study
  publication-title: Front. Oncol.
  doi: 10.3389/fonc.2022.901098
– volume: 126
  start-page: 1625
  year: 1990
  ident: ref30
  article-title: Dual publication and manipulation of the editorial process
  publication-title: Arch. Dermatol.
  doi: 10.1111/j.1525-1470.1990.tb01035.x
– volume: 6
  start-page: 1176
  year: 2012
  ident: ref25
  article-title: Distinct and complex bacterial profiles in human periodontitis and health revealed by 16S pyrosequencing
  publication-title: ISME J.
  doi: 10.1038/ismej.2011.191
– volume: 37
  start-page: S582
  year: 2009
  ident: ref65
  article-title: Resolution of inflammation-unraveling mechanistic links between periodontitis and cardiovascular disease
  publication-title: J. Dent.
  doi: 10.1016/j.jdent.2009.05.013
– volume: 22
  start-page: 292
  year: 2012
  ident: ref38
  article-title: Genomic analysis identifies association of Fusobacterium with colorectal carcinoma
  publication-title: Genome Res.
  doi: 10.1101/gr.126573.111
– volume: 8
  start-page: 1937
  year: 2017
  ident: ref50
  article-title: Insight of genus Corynebacterium: ascertaining the role of pathogenic and non-pathogenic species
  publication-title: Front. Microbiol.
  doi: 10.3389/fmicb.2017.01937
– volume: 9
  start-page: 216
  year: 2019
  ident: ref44
  article-title: Identification of salivary microbiota and its association with host inflammatory mediators in periodontitis
  publication-title: Front. Cell. Infect. Microbiol.
  doi: 10.3389/fcimb.2019.00216
– volume: 43
  start-page: 1
  year: 2021
  ident: ref63
  article-title: Periodontal microorganisms and diagnosis of malignancy: a cross-sectional study
  publication-title: Tumour Biol.
  doi: 10.3233/TUB-200066
– volume: 35
  start-page: 3
  year: 2014
  ident: ref27
  article-title: Immunomicrobial pathogenesis of periodontitis: keystones, pathobionts, and host response
  publication-title: Trends Immunol.
  doi: 10.1016/j.it.2013.09.001
– volume: 5
  start-page: 1571
  year: 2011
  ident: ref32
  article-title: Transitions in bacterial communities along the 2000 km salinity gradient of the Baltic Sea
  publication-title: ISME J.
  doi: 10.1038/ismej.2011.41
– volume: 13
  start-page: 895537
  year: 2022
  ident: ref40
  article-title: The Oral microbiota: community composition, influencing factors, pathogenesis, and interventions
  publication-title: Front. Microbiol.
  doi: 10.3389/fmicb.2022.895537
– volume: 86
  start-page: 611
  year: 2015
  ident: ref21
  article-title: Update on prevalence of periodontitis in adults in the United States: NHANES 2009 to 2012
  publication-title: J. Periodontol.
  doi: 10.1902/jop.2015.140520
– volume: 21
  start-page: 426
  year: 2021
  ident: ref29
  article-title: Local and systemic mechanisms linking periodontal disease and inflammatory comorbidities
  publication-title: Nat. Rev. Immunol.
  doi: 10.1038/s41577-020-00488-6
– volume: 30
  start-page: 11
  year: 2011
  ident: ref2
  article-title: The association of Streptococcus bovis/gallolyticus with colorectal tumors: the nature and the underlying mechanisms of its etiological role
  publication-title: J. Exp. Clin. Cancer Res.
  doi: 10.1186/1756-9966-30-11
– volume: 12
  start-page: 864479
  year: 2022
  ident: ref8
  article-title: Oral microbiota-driven cell migration in carcinogenesis and metastasis
  publication-title: Front. Cell. Infect. Microbiol.
  doi: 10.3389/fcimb.2022.864479
– volume: 48
  start-page: 336
  year: 2021
  ident: ref41
  article-title: Is periodontal disease a risk indicator for colorectal cancer? A systematic review and meta-analysis
  publication-title: J. Clin. Periodontol.
  doi: 10.1111/jcpe.13402
– volume: 32
  start-page: 742
  year: 2020
  ident: ref42
  article-title: Oral microbiome and risk of malignant esophageal lesions in a high-risk area of China: a nested case-control study
  publication-title: Chin. J. Cancer Res.
  doi: 10.21147/j.issn.1000-9604.2020.06.07
– volume: 11
  start-page: 663756
  year: 2021
  ident: ref14
  article-title: Structure and function of Oral microbial Community in Periodontitis Based on integrated data
  publication-title: Front. Cell. Infect. Microbiol.
  doi: 10.3389/fcimb.2021.663756
– volume: 132
  start-page: 87
  year: 2019
  ident: ref13
  article-title: Comparative genomics of the transportome of ten Treponema species
  publication-title: Microb. Pathog.
  doi: 10.1016/j.micpath.2019.04.034
– volume: 87
  start-page: 1016
  year: 2008
  ident: ref36
  article-title: Pyrosequencing analysis of the oral microflora of healthy adults
  publication-title: J. Dent. Res.
  doi: 10.1177/154405910808701104
– volume: 420
  start-page: 860
  year: 2002
  ident: ref16
  article-title: Inflammation and cancer
  publication-title: Nature
  doi: 10.1038/nature01322
– volume: 348
  start-page: 80
  year: 2015
  ident: ref24
  article-title: Cancer and the microbiota
  publication-title: Science
  doi: 10.1126/science.aaa4972
– start-page: 1
  year: 2017
  ident: ref4
  article-title: Permutational multivariate analysis of variance (PERMANOVA)
  publication-title: Wiley StatsRef: Statistics Reference Online
  doi: 10.1002/9781118445112.stat07841
– volume: 13
  start-page: 607
  year: 2012
  ident: ref18
  article-title: Global burden of cancers attributable to infections in 2008: a review and synthetic analysis
  publication-title: Lancet Oncol.
  doi: 10.1016/S1470-2045(12)70137-7
– volume: 34
  start-page: 2193
  year: 2013
  ident: ref46
  article-title: Role of bacterial infections in pancreatic cancer
  publication-title: Carcinogenesis
  doi: 10.1093/carcin/bgt249
– volume: 26
  start-page: 84
  year: 2013
  ident: ref48
  article-title: Bacterial flora of the human oral cavity, and the upper and lower esophagus
  publication-title: Dis. Esophagus
  doi: 10.1111/j.1442-2050.2012.01328.x
– volume: 5
  start-page: e10029
  year: 2010
  ident: ref43
  article-title: Increased throughput by parallelization of library preparation for massive sequencing
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0010029
– volume: 2000
  start-page: 10
  year: 2012
  ident: ref20
  article-title: Global periodontal disease epidemiology
  publication-title: Periodontology
  doi: 10.1111/j.1600-0757.2011.00413.x
– volume: 116
  start-page: 22307
  year: 2019
  ident: ref66
  article-title: Aggregatibacter actinomycetemcomitans colonization and persistence in a primate model
  publication-title: Proc. Natl. Acad. Sci. U. S. A.
  doi: 10.1073/pnas.1905238116
– volume: 15
  start-page: 30
  year: 2015
  ident: ref28
  article-title: Periodontitis: from microbial immune subversion to systemic inflammation
  publication-title: Nat. Rev. Immunol.
  doi: 10.1038/nri3785
– volume: 4
  start-page: 358
  year: 2018
  ident: ref31
  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: 67
  start-page: 1454
  year: 2018
  ident: ref22
  article-title: The oral microbiota in colorectal cancer is distinctive and predictive
  publication-title: Gut
  doi: 10.1136/gutjnl-2017-314814
– volume: 56
  start-page: 622
  year: 2023
  ident: ref54
  article-title: Microbiome in paired root apices and periapical lesions and its association with clinical signs in persistent apical periodontitis using next-generation sequencing
  publication-title: Int. Endod. J.
  doi: 10.1111/iej.13893
– volume: 510
  start-page: 92
  year: 2014
  ident: ref61
  article-title: Pro-resolving lipid mediators are leads for resolution physiology
  publication-title: Nature
  doi: 10.1038/nature13479
– volume: 100
  start-page: 37
  year: 2021
  ident: ref57
  article-title: Periodontitis, Edentulism, and risk of mortality: a systematic review with Meta-analyses
  publication-title: J. Dent. Res.
  doi: 10.1177/0022034520952401
– volume: 57
  start-page: 406
  year: 2012
  ident: ref17
  article-title: Signaling pathways involved in the regulation of TNFalpha-induced toll-like receptor 2 expression in human gingival fibroblasts
  publication-title: Cytokine
  doi: 10.1016/j.cyto.2011.12.008
– volume: 78
  start-page: 1387
  year: 2007
  ident: ref52
  article-title: Case definitions for use in population-based surveillance of periodontitis
  publication-title: J. Periodontol.
  doi: 10.1902/jop.2007.060264
– volume: 83
  start-page: e00462-17
  year: 2017
  ident: ref45
  article-title: Signature of microbial Dysbiosis in periodontitis
  publication-title: Appl. Environ. Microbiol.
  doi: 10.1128/AEM.00462-17
– start-page: 65
  year: 2000
  ident: ref6
  article-title: Oral ecology and person-to-person transmission of Actinobacillus actinomycetemcomitans and Porphyromonas gingivalis
  publication-title: Periodontology
  doi: 10.1111/j.1600-0757.1999.tb00158.x
– volume: 2
  start-page: 722495
  year: 2021
  ident: ref34
  article-title: Oral Dysbiosis in severe forms of periodontitis is associated with gut Dysbiosis and correlated with salivary inflammatory mediators: a preliminary study
  publication-title: Front Oral Health
  doi: 10.3389/froh.2021.722495
– volume: 9
  start-page: 1603
  year: 2018
  ident: ref19
  article-title: Microbial similarity and preference for specific sites in healthy Oral cavity and esophagus
  publication-title: Front. Microbiol.
  doi: 10.3389/fmicb.2018.01603
SSID ssj0000402000
Score 2.376136
Snippet Periodontitis is one of the world’s most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the...
Periodontitis is one of the world's most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the...
SourceID doaj
pubmedcentral
proquest
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 1172340
SubjectTerms 16S rRNA gene sequencing
cancer
malignancy
Microbiology
oral microbiota
periodontitis
supragingival plaque
SummonAdditionalLinks – databaseName: Directory of Open Access Journals - May need to register for free articles
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1NS8QwEA0iCF7Eb9cvIniTajdtk-5RRRFBTwreQqZJdEG74u4e9uaP8Bf6S5xJusuuiF48tk3bNG_SvEkmbxg7zKBsV4UTCSC8Sa6UTcqOMgmS6zx1VqRK0N7hm1t5dZ9fPxQPU6m-KCYsygPHhjtRTgjfDstNKpe2APBISnwbhHRg8qBeimPelDMV_sHkFqVp3CWDXlgHYepWcEzJwmmdUmQ02zE1EgXB_p9Y5vdgyanR53KZLTW0kZ_G6q6wOVevsoWYSHK0xkbUrZvwK97zvD8ESj7URTPiL92otTQw3DRYOMtp_pWTyjG6pUFWtc9NbbmNkXd4hE95QY7-SIIco8_3D8PDZyT9ELtFlQnKtOvs_vLi7vwqaZIqJBVSv0GiZJV2SPRLegkdCZk3qgQJpigcJetU3jmJpARpliSxM0tzQ5mVKTa69ejPbrD5ule7LcaFFE5aCxmWQR4ApXPICKT3YCqbFdBi7XED66pRHKfEF88aPQ8CRQdQNIGiG1Ba7Ghyz2vU2_i19BnhNilJWtnhBFqQbixI_2VBLXYwRl1j36IFE1O73rCvBbFH9NQFltmMVjB5VaZI21-oFitn7GOmLrNX6u5T0O8mDUPSGNr-j9rvsEVqkTgrtMvmB29Dt4c8aQD7oUt8AfihE0U
  priority: 102
  providerName: Directory of Open Access Journals
Title Composition of subgingival microbiota associated with periodontitis and diagnosis of malignancy—a cross-sectional study
URI https://www.ncbi.nlm.nih.gov/pubmed/37426027
https://www.proquest.com/docview/2839252325
https://pubmed.ncbi.nlm.nih.gov/PMC10325785
https://doaj.org/article/7e22f164078746d5bbf192f1b26eba45
Volume 14
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1da9swFBWlZbCXsXZfWT_QYG_DxZZtyXkooy39YNA9LZA3oWtJXaB1tjiB5q0_or-wv2T3ykpoStenvhhiy7GioxudK8nnMPY1hyqrSycSQHiTQimbVH1lEiTXReqsSJWgd4cvfsrzQfFjWA7X2MLuKDZg-2RqR35Sg8nV_s3f-XcM-APKOHG8RQRGNeyTDzgtQYq8wBR-A0cmRY4GF5Huh39mSpbStHt35j-3roxPQcb_Ke75eAvlgzHp9C17E8kkP-zQ32Rrrtlirzp7yfk7Nqdgj5uy-NjzdgZkSTTCzsWvR50C09RwExFyltOsLCftY0xWg9hqy01jue324-En_JZrZO6XJNMxv7-9Mzz8jKQNO7qoMkGv9j0bnJ78Oj5PotVCUiMhnCZK1mmfpMCkl9CXkHujKpBgytKRhafyzkmkKki-JEmgWZoxyq1M-8Jbj1nuB7bejBv3iXEhhZPWQo5lkB1A5RzyBOk9mNrmJfRYtmhgXUcdcrLDuNKYjxAoOoCiCRQdQemxb8t7_nQqHM-WPiLcliVJQTucGE8udQxIrZwQPgvLmKqQtgTwSHZ9BkI6MEXZY18WqGuMOFpGMY0bz1otiFNi_i6wzMeuFywflStS_Beqx6qV_rFSl9Urzeh3UPUmZUNSHvr8ErXfZq-pRbq5oh22Pp3M3C6ypynshVkHPJ4Ns70QHv8AACUdwg
linkProvider Scholars Portal
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Composition+of+subgingival+microbiota+associated+with+periodontitis+and+diagnosis+of+malignancy%E2%80%94a+cross-sectional+study&rft.jtitle=Frontiers+in+microbiology&rft.au=Aswathy+Narayanan&rft.au=Aswathy+Narayanan&rft.au=Birgitta+S%C3%B6der&rft.au=Jukka+Meurman&rft.date=2023&rft.pub=Frontiers+Media+S.A&rft.eissn=1664-302X&rft.volume=14&rft_id=info:doi/10.3389%2Ffmicb.2023.1172340&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_7e22f164078746d5bbf192f1b26eba45
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1664-302X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1664-302X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1664-302X&client=summon