Risk factors for malignant oral mucosal lesion development (literature review). Part 2. Exogenous factors
https://doi.org/10.33925/1683-3031-2023-624
Abstract
Relevance. Cancer stands as a prominent cause of untimely mortality in young and middle-aged individuals (aged 20-64 years). The inquiry into the extent of influence exerted by external risk factors on the emergence of oral mucosal oncopathology remains pertinent. Equally crucial is understanding the intricate interplay among different groups of factors and their effects.
Research objective. To determine the extent of influence exerted by various endogenous and exogenous risk factors on the development of malignant oral mucosal lesions, based on contemporary literature data, and to assess their interrelationships.
Materials and methods. The research material was the analysis of literary data from bibliographic sources – Elsevier, PubMed, Elibrary, Google Academy, Medline, Cyberleninka. The study included literature sources in Russian and English. The second part of the review combines studies devoted to the study of the influence of exogenous controlled factors on the risk of developing malignant neoplasms of the oral mucosa.
Results. Through contemporary literature analysis, the potential and scale of influence attributed to controllable exogenous risk factors in the development of malignant oral mucosal lesions have been established. Notably, significant impact has been associated with smoking and alcohol consumption. Additionally, adverse socio-economic conditions, environmental factors, and dietary habits have been identified as contributors to an elevated cancer risk. Throughout this investigation, it became evident that literature sources frequently highlight the influence of individual factors without adequately considering potential synergies, antagonistic effects, or interactions with endogenous factors. Moreover, certain factors pivotal to the carcinogenesis of oral cavity tumors remain inadequately researched.
Conclusion. To facilitate efficient primary and secondary prevention measures, it is imperative to advance and refine a multidisciplinary research methodology. This approach should aim to comprehensively identify the collective impact of diverse groups of risk factors on the progression of malignant oral mucosal lesions.
About the Authors
Yu. V. LunitsynaRussian Federation
Yulia V. Lunitsyna, DMD, PhD, Associate Professor, Department of Operative Dentistry
Barnaul
A. F. Lazarev
Russian Federation
Alexander F. Lazarev, MD, PhD, DSc, Professor, Department of Oncology and Radiation Therapy with the Course of Continuing Professional Education
Barnaul
S. I. Tokmakova
Russian Federation
Svetlana I. Tokmakova, DMD, PhD, DSc, Professor, Head of the Department of Operative Dentistry
Barnaul
O. V. Bondarenko
Russian Federation
Olga V. Bondarenko, DMD, PhD, Associate Professor, Department of Operative Dentistry
Barnaul
References
1. O'Grady I, Anderson A, O'Sullivan J. The interplay of the oral microbiome and alcohol consumption in oral squamous cell carcinomas. Oral Oncol. 2020;110:105011. doi: 10.1016/j.oraloncology.2020.105011
2. Kirtayeva AV, Gazhva SI, Trofimova IN, Ilyina SP. The effect of alcohol on the oral cavity. Zdravooxranenie Chuvashii. 2020;1:60 (In Russ.). doi: 10.25589/GIDUV.2020.63.67.007
3. Goryainova GN, Litvinova ES. Characteristics of risk factors and pathomorphology of cancer of the oral mucosa. Regional`ny`j vestnik. 2020;(10):30-31. (In Russ.). Available from: https://elibrary.ru/item.asp?id=43090485
4. Gormley M, Dudding T, Sanderson E, Martin RM, Thomas S, Tyrrell J, et al. A multivariable Mendelian randomization analysis investigating smoking and alcohol consumption in oral and oropharyngeal cancer. Nat Commun. 2020;11(1):6071. doi: 10.1038/s41467-020-19822-6.
5. Hashibe M, Brennan P, Benhamou S, Martin RM, Thomas S, Tyrrell J, et al. Alcohol drinking in never users of tobacco, igarette smoking in never drinkers, and the risk of head and neck cancer: pooled analysis in the International Head and Neck Cancer Epidemiology Consortium. J Natl Cancer Inst. 2007;99(10):777-89. doi: 10.1093/jnci/djk179.
6. Berthiller J, Straif K, Agudo A, Ahrens W, Dos Santos AB, Boccia S, et al. Low frequency of cigarette smoking and the risk of head and neck cancer in the INHANCE consortium pooled analysis. Int J Epidemiol. 2016;45(3):835-45. doi: 10.1093/ije/dyv146
7. Lubin JH, Purdue M, Kelsey K, Zhang ZF, Winn D, Wei Q, et al. Total exposure and exposure rate effects for alcohol and smoking and risk of head and neck cancer: a pooled analysis of case-control studies. Am J Epidemiol. 2009;170(8):937-47. doi: 10.1093/aje/kwp222.
8. Conway DI, Purkayastha M, Chestnutt IG. The changing epidemiology of oral cancer: definitions, trends, and risk factors. Br Dent J. 2018;225(9):867-873. doi: 10.1038/sj.bdj.2018.922
9. Anders WM, Bull R, Cantor K, Chakraborti D, Chen C, DeAngelo AB. IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. 1987. Available from: https://www.researchgate.net/publication/37621754_IARC_Monographs_on_the_Evaluation_of_Carcinogenic_Risks_to_Humans
10. Balbo S, Brooks PJ, editors. Implications of Acetaldehyde-Derived DNA Adducts for Understanding Alcohol-Related Carcinogenesis. Biological Basis of Alcohol Induced Cancer. 2015. doi: 10.1007/978-3-319-09614-8_5.
11. Balbo S, Juanes RC, Khariwala S, Baker EJ, Daunais JB, Grant KA. Increased levels of the acetaldehyde-derived DNA adduct N 2-ethyldeoxyguanosine in oral mucosa DNA from Rhesus monkeys exposed to alcohol. Mutagenesis. 2016;31(5):553–558. doi: 10.1093/mutage/gew016.
12. Hashibe M, Brennan P, Chuang SC, Boccia S, Castellsgue X, Chen Ch, et al. Interaction between tobacco and alcohol use and the risk of head and neck cancer: pooled analysis in the International Head and Neck Cancer Epidemiology Consortium. Cancer Epidemiol Biomarkers Prev. 2009;18(2):541-550. doi: 10.1158/1055-9965.EPI-08-0347
13. Speight PM, Khurram SA, Kujan O. Oral potentially malignant disorders: risk of progression to malignancy. Oral Surg Oral Med Oral Pathol Oral Radiol. 2018;125(6):612-627. doi: 10.1016/j.oooo.2017.12.011
14. Edirisinghe ST, Weerasekera M, De Silva DK, Liyanage I, Niluka M, Madushika K, et al. The Risk of Oral Cancer among Different Categories of Exposure to Tobacco Smoking in Sri Lanka. Asian Pac J Cancer Prev. 2022;23(9):2929-2935. doi: 10.31557/APJCP.2022.23.9.2929.
15. Croucher R, Dahiya M, Gowda KK. Contents and price of vendor assembled paan quid with tobacco in five London localities: a cross-sectional study. Tob Control. 2013;22(2):141-143. doi: 10.1136/tobaccocontrol-2012-050564
16. Siddiqi K, Gupta PC, Prasad VM, Croucher R, Sheikh A. Smokeless tobacco use by south Asians. Lancet Glob Health. 2013;1(2):e71. doi: 10.1016/S2214-109X(13)70021-4
17. Wyss AB, Hashibe M, Lee YA, Chuang ShCh, Muscat J, Chen C, et al. Smokeless tobacco use and the risk of head and neck cancer: pooled analysis of US studies in the INHANCE Consortium. Am J Epidemiol. 2016;184(10):703-716. doi: 10.1093/aje/kww075
18. Conway DI, Brenner D R, McMahon AD, Macpherson LMD, Agudo A, Ahrens W, et al. Estimating and explaining the effect of education and income on head and neck cancer risk: INHANCE consortium pooled analysis of 31 case-control studies from 27 countries. Int J Cancer. 2015;136(5):1125-1139. doi: 10.1002/ijc.29063
19. Aleksandrovich OV. Socio-cultural assessment cancer incidence. Law and global society. 2016;(3):65-72 (In Russ.). Available from: https://www.elibrary.ru/item.asp?id=27692189
20. Mikhalkina, EV, Skachkova, LS, Kit OI, Fomenko YuA. Socio-economic predictors of cancers. Journal of Institutional Studies. 2020;12(3),122-141 (In Russ.). doi: 10.17835/2076-6297.2020.12.3.122-141
21. Freire AR, Freire DEWG, Araújo ECF, de Lucena EHG, Cavalcanti YW. Influence of Public Oral Health Services and Socioeconomic Indicators on the Frequency of Hospitalization and Deaths due to Oral Cancer in Brazil, between 2002-2017. Int J Environ Res Public Health. 2020;18(1):238. doi: 10.3390/ijerph18010238.
22. Azimi S, Rafieian N, Manifar S, Ghorbani Z, Tennant M, Kruger E. Socioeconomic determinants as risk factors for squamous cell carcinoma of the head and neck: a case-control study in Iran. Br J Oral Maxillofac Surg. 2018;56(4):304-309. doi: 10.1016/j.bjoms.2018.02.014.
23. Edefonti V, Hashibe M, Ambrogi F, Parpinel M, Bravi F, Talamini R, et al. Nutrient-based dietary patterns and the risk of head and neck cancer: a pooled analysis in the International Head and Neck Cancer Epidemiology consortium. Ann Oncol. 2012;3(7):1869-1880 doi:10.1093/annonc/mdr548
24. Rodríguez-Molinero J, Migueláñez-Medrán BDC, Puente-Gutiérrez C, Delgado-Somolinos E, Martín Carreras-Presas C, Fernández-Farhall J, et al. Association between Oral Cancer and Diet: An Update. Nutrients. 2021;13(4):1299. doi: 10.3390/nu13041299
25. Leoncini E, Edefonti V, Hashibe M, Parpinel M, Cadoni G, Ferraroni M, et al. Carotenoid intake and head and neck cancer: a pooled analysis in the International Head and Neck Cancer Epidemiology Consortium. Eur J Epidemiol. 2016;31(4):369-383 doi: 10.1007/s10654-015-0036-3
26. Zakrevskiy VV, Liflyandskiy VG. Vegetables and fruits in the prevention and treatment of cancer in the light of evidence-based medicine (part 1). Bulletin of St. Petersburg University. Medicine. 2017;12(4):407-418 (In Russ.). Available from: https://medicine-journal.spbu.ru/article/view/5846
27. Tapia J L, Goldberg L J. The challenges of defining oral cancer: Analysis of an ontological approach. Head Neck Pathol. 2011;5(4):376-384. doi: 10.1007/s12105-011-0300-0
28. Modenese A, Korpinen L, Gobba F. Solar Radiation Exposure and Outdoor Work: An Underestimated Occupational Risk. Int J Environ Res Public Health. 2018;15(10):2063. doi: 10.3390/ijerph15102063
Review
For citations:
Lunitsyna Yu.V., Lazarev A.F., Tokmakova S.I., Bondarenko O.V. Risk factors for malignant oral mucosal lesion development (literature review). Part 2. Exogenous factors. Pediatric dentistry and dental prophylaxis. 2023;23(4):397-404. (In Russ.) https://doi.org/10.33925/1683-3031-2023-624