Skip to main content
Cancers logoLink to Cancers
editorial
. 2023 Mar 13;15(6):1736. doi: 10.3390/cancers15061736

Periodontitis and Cancer: Beyond the Boundaries of Oral Cavity

Alessandra Amato 1
PMCID: PMC10046642  PMID: 36980622

Oral squamous cell carcinoma (OSCC) is the 16th most common cancer and the 15th leading cause of death worldwide, with an incidence of 4 cases per 100,000 people [1]. The main risk factors for OSCC are smoking and excessive alcohol consumption, associated with approximately 75% of cases [2]. Other risk factors include irritation of the mucosa due to trauma caused by dentures and rough tooth surfaces, poor nutrition, some chronic infections caused by specific microorganisms [2], such as Human Papillomavirus [3], Epstein–Barr virus [4], and Candida Albicans [5], and poor oral hygiene. The association between poor oral hygiene and oral cancer has been suspected for decades [6]. In recent years, oral dysbiosis, altering the fine equilibrium among microorganisms coexisting in the oral cavity and forming a large ecological community, with oral [7,8] and systemic health [9] relapses [10], as well as periodontitis have been implied in oral carcinogenesis [6].

Periodontitis is a microbially associated inflammatory disease [11] that commonly occurs in adulthood [12] and is characterized by periodontal tissue destruction and alveolar bone loss [13,14,15], which can lead to tooth loss [16]. According to the Global Burden of Disease Study, periodontitis prevalence has increased by 57.3% from 1990 to 2010 and currently represents the sixth most common disease worldwide, and affects about 743 million people, accounting for the 11.2% of the total world population [17], 10% of whom with severe periodontitis [18].

The association between periodontitis and OSCC may rely on periodontal and interrelated systemic inflammation, as hypothesized for several systemic inflammatory and degenerative diseases, including atherosclerosis, Alzheimer’s disease, age-related macular degeneration, and chronic bowel disease [19,20]. Indeed, chronic inflammatory processes were first linked to the development of cancer by Virchow in the 19th century. To date, 15–20% of human cancers are estimated to originate from an inflammatory process that promotes cell proliferation and malignant transformation [21]. Specifically, in animal models of periodontal biofilm-induced oral carcinogenesis, a higher incidence of epithelial dysplasia and oral carcinoma was found than in tobacco surrogate-induced carcinogenesis; a larger tumor size and a more marked reduction in the protective mechanisms of epithelial cell differentiation were also observed [6]. Moreover, more severe forms of periodontitis were correlated with a higher incidence of OSCC [22]. Most studies [23,24,25] specifically investigated the putative indirect oncogenic role of Porphyromonas gingivalis [23] in the initiation and development of OSCC [24,25,26].

Furthermore, oral dysbiosis underlying periodontitis has been associated with several malignancies [7] including lung [8], prostate [9], colon [10], pancreas [7], breast [27], head and neck [28], and oral cavity cancers [29,30]. The oral and periodontal microbiome could promote carcinogenesis at extraoral sites through systemic inflammation, indirect long-distance action of virulence factors from oral microbiota, direct translocation of microorganisms through the bloodstream, oropharyngeal, and respiratory tracts, or by influencing the response to treatments through interaction with the host immune response [31].

Periodontitis, especially in moderate or severe cases, has been associated with an increased risk of dying from cancer of the oral and digestive tract [26]. In addition, periodontitis has been reported to be an independent risk factor for the occurrence of complications in cancer patients undergoing gastrointestinal surgery for cancer [32]. In addition, the finding of an association between elevated serum IgG for Porphyromonas gingivalis and higher mortality for orodigestive cancers in both periodontitis and periodontally healthy individuals suggests a possible specific role of periodontal bacteria in the development of extraoral oncogenesis, independent of the presence of periodontitis [26].

Further studies are needed to understand the potential role of periodontitis, particularly some periodontal pathogens, in developing OSCC and extraoral cancers and the impact of periodontitis on cancer progression and patient outcomes for the multidisciplinary management of cancer patients with periodontitis [33,34].

Conflicts of Interest

The author declares no conflict of interest.

Footnotes

Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

References

  • 1.Inchingolo F., Santacroce L., Ballini A., Topi S., Dipalma G., Haxhirexha K., Bottalico L., Charitos I.A. Oral Cancer: A Historical Review. Int. J. Environ. Res. Public Health. 2020;17:3168. doi: 10.3390/ijerph17093168. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Ye L., Jiang Y., Liu W., Tao H. Correlation between Periodontal Disease and Oral Cancer Risk: A Meta-Analysis. J. Cancer Res. Ther. 2016;12:237. doi: 10.4103/0973-1482.200746. [DOI] [PubMed] [Google Scholar]
  • 3.Hübbers C.U., Akgül B. HPV and Cancer of the Oral Cavity. Virulence. 2015;6:244–248. doi: 10.1080/21505594.2014.999570. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Guidry J., Birdwell C., Scott R. Epstein-Barr Virus in the Pathogenesis of Oral Cancers. Oral Dis. 2018;24:497–508. doi: 10.1111/odi.12656. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Ayuningtyas N.F., Mahdani F.Y., Pasaribu T.A.S., Chalim M., Ayna V.K.P., Santosh A.B.R., Santacroce L., Surboyo M.D.C. Role of Candida Albicans in Oral Carcinogenesis. Pathophysiology. 2022;29:650–662. doi: 10.3390/pathophysiology29040051. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Spuldaro T., Wagner V., Nör F., Gaio E., Squarize C., Carrard V., Rösing C., Castilho R. Periodontal Disease Affects Oral Cancer Progression in a Surrogate Animal Model for Tobacco Exposure. Int. J. Oncol. 2022;60:77. doi: 10.3892/ijo.2022.5367. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Bracci P.M. Oral Health and the Oral Microbiome in Pancreatic Cancer. Cancer J. 2017;23:310–314. doi: 10.1097/PPO.0000000000000287. [DOI] [PubMed] [Google Scholar]
  • 8.Wadia R. Periodontal Disease & Lung Cancer. Br. Dent. J. 2020;229:125. doi: 10.1038/s41415-020-1952-5. [DOI] [PubMed] [Google Scholar]
  • 9.Guo Z., Gu C., Li S., Gan S., Li Y., Xiang S., Gong L., Wang S. Periodontal Disease and the Risk of Prostate Cancer: A Meta-Analysis of Cohort Studies. Int. Braz. J. Urol. 2021;47:1120–1130. doi: 10.1590/s1677-5538.ibju.2020.0333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.O’Rourke K. Periodontal Disease Linked to an Increase in Colorectal Cancer. Cancer. 2022;128 doi: 10.1002/cncr.34204. [DOI] [PubMed] [Google Scholar]
  • 11.Di Spirito F., Schiavo L., Pilone V., Lanza A., Sbordone L., D’Ambrosio F. Periodontal and Peri-Implant Diseases and Systemically Administered Statins: A Systematic Review. Dent. J. 2021;9:100. doi: 10.3390/dj9090100. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Billings M., Holtfreter B., Papapanou P.N., Mitnik G.L., Kocher T., Dye B.A. Age-Dependent Distribution of Periodontitis in Two Countries: Findings from NHANES 2009 to 2014 and SHIP-TREND 2008 to 2012. J. Periodontol. 2018;89:S140–S158. doi: 10.1002/JPER.17-0670. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Sbordone C., Toti P., Brevi B., Martuscelli R., Sbordone L., Di Spirito F. Computed Tomography-Aided Descriptive Analysis of Maxillary and Mandibular Atrophies. J. Stomatol. Oral Maxillofac. Surg. 2019;120:99–105. doi: 10.1016/j.jormas.2018.12.006. [DOI] [PubMed] [Google Scholar]
  • 14.Di Spirito F., Toti P., Brevi B., Martuscelli R., Sbordone L., Sbordone C. Computed Tomography Evaluation of Jaw Atrophies before and after Surgical Bone Augmentation. Int. J. Clin. Dent. 2019;12:259–270. [Google Scholar]
  • 15.Ramaglia L., Di Spirito F., Sirignano M., la Rocca M., Esposito U., Sbordone L. A 5-year Longitudinal Cohort Study on Crown to Implant Ratio Effect on Marginal Bone Level in Single Implants. Clin. Implant Dent. Relat. Res. 2019;21:916–922. doi: 10.1111/cid.12757. [DOI] [PubMed] [Google Scholar]
  • 16.Di Spirito F., la Rocca M., de Bernardo M., Rosa N., Sbordone C., Sbordone L. Possible Association of Periodontal Disease and Macular Degeneration: A Case-Control Study. Dent. J. 2020;9:1. doi: 10.3390/dj9010001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Tonetti M.S., Jepsen S., Jin L., Otomo-Corgel J. Impact of the Global Burden of Periodontal Diseases on Health, Nutrition and Wellbeing of Mankind: A Call for Global Action. J. Clin. Periodontol. 2017;44:456–462. doi: 10.1111/jcpe.12732. [DOI] [PubMed] [Google Scholar]
  • 18.Khajavi A., Radvar M., Moeintaghavi A. Socioeconomic Determinants of Periodontitis. Periodontol 2000. 2022;90:13–44. doi: 10.1111/prd.12448. [DOI] [PubMed] [Google Scholar]
  • 19.Di Spirito F., Iandolo A., Amato A., Caggiano M., Raimondo A., Lembo S., Martina S. Prevalence, Features and Degree of Association of Oral Lesions in COVID-19: A Systematic Review of Systematic Reviews. Int. J. Environ. Res. Public Health. 2022;19:7486. doi: 10.3390/ijerph19127486. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Di Spirito F., Sbordone L., Pilone V., D’Ambrosio F. Obesity and Periodontal Disease: A Narrative Review on Current Evidence and Putative Molecular Links. Open Dent. J. 2019;13:526–536. doi: 10.2174/1874210601913010526. [DOI] [Google Scholar]
  • 21.Colonia-García A., Gutiérrez-Vélez M., Duque-Duque A., de Andrade C.R. Possible Association of Periodontal Disease with Oral Cancer and Oral Potentially Malignant Disorders: A Systematic Review. Acta Odontol. Scand. 2020;78:553–559. doi: 10.1080/00016357.2020.1774076. [DOI] [PubMed] [Google Scholar]
  • 22.de Rezende C.P., Ramos M.B., Daguíla C.H., Dedivitis R.A., Rapoport A. Oral Health Changes in Patients with Oral and Oropharyngeal Cancer. Braz. J. Otorhinolaryngol. 2008;74:596–600. doi: 10.1016/S1808-8694(15)30609-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Amato M., Di Spirito F., D’Ambrosio F., Boccia G., Moccia G., de Caro F. Probiotics in Periodontal and Peri-Implant Health Management: Biofilm Control, Dysbiosis Reversal, and Host Modulation. Microorganisms. 2022;10:2289. doi: 10.3390/microorganisms10112289. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Katz J., Onate M.D., Pauley K.M., Bhattacharyya I., Cha S. Presence of Porphyromonas Gingivalis in Gingival Squamous Cell Carcinoma. Int. J. Oral Sci. 2011;3:209–215. doi: 10.4248/IJOS11075. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Atanasova K.R., Yilmaz Ö. Looking in the Porphyromonas Gingivalis Cabinet of Curiosities: The Microbium, the Host and Cancer Association. Mol. Oral Microbiol. 2014;29:55–66. doi: 10.1111/omi.12047. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Ahn J., Segers S., Hayes R.B. Periodontal Disease, Porphyromonas Gingivalis Serum Antibody Levels and Orodigestive Cancer Mortality. Carcinogenesis. 2012;33:1055–1058. doi: 10.1093/carcin/bgs112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Söder B., Yakob M., Meurman J.H., Andersson L.C., Klinge B., Söder P.-Ö. Periodontal Disease May Associate with Breast Cancer. Breast Cancer Res. Treat. 2011;127:497–502. doi: 10.1007/s10549-010-1221-4. [DOI] [PubMed] [Google Scholar]
  • 28.Moraes R.C.d., Dias F.L., Figueredo C.M.d.S., Fischer R.G. Association between Chronic Periodontitis and Oral/Oropharyngeal Cancer. Braz. Dent. J. 2016;27:261–266. doi: 10.1590/0103-6440201600754. [DOI] [PubMed] [Google Scholar]
  • 29.Javed F., Warnakulasuriya S. Is There a Relationship between Periodontal Disease and Oral Cancer? A Systematic Review of Currently Available Evidence. Crit. Rev. Oncol. Hematol. 2016;97:197–205. doi: 10.1016/j.critrevonc.2015.08.018. [DOI] [PubMed] [Google Scholar]
  • 30.Di Spirito F., Argentino S., Martuscelli R., Sbordone L. MRONJ incidence after multiple teeth extractions in patients taking oral bisphosphonates without “drug holiday”: A retrospective chart review. Oral Implantol. 2019;12:105–110. [Google Scholar]
  • 31.Di Spirito F. Oral-Systemic Health and Disorders: Latest Prospects on Oral Antisepsis. Appl. Sci. 2022;12:8185. doi: 10.3390/app12168185. [DOI] [Google Scholar]
  • 32.Nishikawa M., Honda M., Kimura R., Kobayashi A., Yamaguchi Y., Kobayashi H., Kawamura H., Nakayama Y., Todate Y., Takano Y., et al. Clinical Impact of Periodontal Disease on Postoperative Complications in Gastrointestinal Cancer Patients. Int. J. Clin. Oncol. 2019;24:1558–1564. doi: 10.1007/s10147-019-01513-y. [DOI] [PubMed] [Google Scholar]
  • 33.Di Spirito F., Iacono V.J., Alfredo I., Alessandra A., Sbordone L., Lanza A. Evidence-Based Recommendations on Periodontal Practice and the Management of Periodontal Patients During and After the COVID-19 Era: Challenging Infectious Diseases Spread by Airborne Transmission. Open Dent. J. 2021;15:325–336. doi: 10.2174/1874210602115010325. [DOI] [Google Scholar]
  • 34.Di Spirito F., Pelella S., Argentino S., Sisalli L., Sbordone L. Oral Manifestations and the Role of the Oral Healthcare Workers in COVID-19. Oral Dis. 2022;28:1003–1004. doi: 10.1111/odi.13688. [DOI] [PubMed] [Google Scholar]

Articles from Cancers are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES