|DENTAL SCIENCE - REVIEW ARTICLE
|Year : 2015 | Volume
| Issue : 5 | Page : 162-164
Candida in potentially malignant oral disorders
S Leena Sankari, K Gayathri, N Balachander, L Malathi
Department of Oral Pathology and Microbiology, Sree Balaji Dental College and Hospitals, Bharath University, Chennai, Tamil Nadu, India
|Date of Submission||31-Oct-2014|
|Date of Decision||31-Oct-2014|
|Date of Acceptance||09-Nov-2014|
|Date of Web Publication||30-Apr-2015|
Department of Oral Pathology and Microbiology, Sree Balaji Dental College and Hospitals, Bharath University, Chennai, Tamil Nadu
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Oro-pharyngeal cancer is a significant component in the global burden of cancer. A considerable proportion of oral squamous carcinomas develop from preexsiting potentially malignant disorder of the oral cavity. The term potentially malignant oral disorders (PMD) were proposed for the precancerous lesions and conditions by World Health Organization in 2007. PMD are considered an in-between clinical state, which showed increased risk for cancer development. Etiology of PMD is multifactorial. Tobacco and alcohol are the major risk factors. In recent years, role of candidal infection is recognized as a significant factor in the development of PMD. There is an enduring discussion whether Candida infection can be a cause of PMD or a superimposed infection in a preexisting lesion. This article highlights the association between Candida and PMD.
Keywords: Candida , carcinogen, potentially malignant oral disorders
|How to cite this article:|
Sankari S L, Gayathri K, Balachander N, Malathi L. Candida in potentially malignant oral disorders. J Pharm Bioall Sci 2015;7, Suppl S1:162-4
Oro-pharyngeal cancer is a significant component of the global burden of cancer. The occurrence of oral cancer is particularly high among men and is the eighth most common cancer worldwide.  A considerable proportion of oral squamous carcinomas develop from preexisting potentially malignant disorder of the oral cavity.  World Health Organization (WHO) in 2007 proposed the term potentially malignant oral disorders (PMD) for precancerous lesions and conditions.  Oral precancer is considered intermediate clinical state that showed increased risk for cancer development. If recognized and treated early they show better prognosis. , Etiology of potentially malignant disorders are multifactorial. Tobacco and alcohol are considered a major risk factors but increasingly the role of viral and candidal infection are recognized as being significant in cancer development. 
Candida spp. is normal commensal fungi that are found colonizing the oral mucosa frequently. Oral Candida is "opportunistic pathogens". Depending on the host defense mechanisms or local oral microenvironment, Candida can transform from a harmless commensal to the pathogenic organism causing oral mucosal infection. , This article highlights the association between Candida and PMD.
| Candida|| |
Candida is a yeast-like fungi. Candida is derived from Latin word where toga Candida was a white robe worn by Roman Senators.  Candida comes under the phylum, Ascomycota and order, Saccharomycetales. It is a pathogenic dimorphic yeast-like fungi. In host tissues or cultures at 37°C, they occur as yeasts. In soil and in culture at 22°C, they appear as molds.  Currently, there are some 200 organism species within the genus Candida. Of the nearly 200 species, six species, Candida albicans, Candida glabrata, Candida tropicalis, Candida parapsilosis, Candida krusei, and Candida lusitaniae are the most commonly associated with human infection.  Diagnosis can be done using methods like microscopic examination, culture methods, proteomic and genomic studies.
Depending on the host defense mechanisms or local oral microenvironment Candida can transform from a harmless commensal to the pathogenic organism causing oral mucosal infection. Some conditions in which Candida can become pathogenic are old age, smoking, diabetes, malignancies, radiation exposure and immunocompromised states like HIV.
Phenotypic switching of Candida is noticed when they become pathogenic and invade the tissues. Yeast cells adhere to both oral and intestinal epithelia and then rapidly switch to hyphal growth. Adherence is mediated by a range of cell wall proteins that are expressed on the surface of hyphal cells.  Two mechanisms are proposed for phenotypic switching. First mechanism is by secretion of degradative enzymes by the fungus-like proteases that might digest epithelial cell surface components. This in turn allows the physical movement of hyphae into/between the host cells. The second mechanism is by the initiation of epithelial cell endocytosis. 
| Potentially Malignant Oral Disorders|| |
World Health Organization proposed in 1978  defined precancerous lesions as a morphologically altered tissue in which oral cancer is more likely to occur than in its apparently normal counterpart' and precancerous condition as a generalized state associated with a significantly increased risk of cancer'. Precancerous lesions include leukoplakia, erythroplakia, palatal lesions in reverse smokers.
Precancerous conditions are oral submucous fibrosis (OSMF), lichen planus, discoid lupus erythematosus, sideropenic dysphagia, syphilis, xeroderma pigmentosum, epidermolysis bullosa (WHO 1997).  WHO collaborating center for oral precancerous lesions in 2007 recommend the term "potentially malignant disorders," as it conveys that not all lesions and conditions described under this term may transform to cancer.  Among them frequently associated lesions with Candida is leukoplakia. Others are erythroplakia, OSMF, and lichen planus.
Leukoplakia means a "white patch", which is derived from Greek words "leucos" means white and "plakia" means patch. It was defined as "a white patch or plaque that cannot be characterized clinically or pathologically as any other disease". Tobacco has been incriminated as a major etiological agent in the development of potentially malignant lesions. The role of C. albicans as a possible etiological factor in leukoplakia and its possible role in malignant transformation is still unclear.
Two main clinical types of leukoplakia are homogeneous and nonhomogeneous leukoplakia . Homogeneous lesions are uniformly thin, flat and show shallow cracks on the surface keratin. Nonhomogeneous varieties comprise speckled, nodular and verrucous types.  The current way for predicting the malignant potential of premalignant lesions is the by looking for the presence and degree of dysplasia.
Oral submucous fibrosis
Oral submucous fibrosis is an insidious chronic disease affecting any part of the oral cavity and sometimes pharynx. It is constantly associated with juxta-epithelial inflammatory reaction followed by fibro-elastic change in lamina propria and epithelial atrophy; which leads to stiffness of the oral mucosa, causing trismus and inability to eat. 
A multifactorial model for the pathogenesis of OSMF is postulated. Tobacco, lime, betel quid, iron and nutritional deficiencies, chronic candidiasis, genetic abnormalities, viral infections, autoimmunity etc., are considered to have either direct effect in causing OSMF or an indirect effect by intervening the immune system which is compromised in OSMF. 
Lichen planus is an autoimmune immune disease of unknown etiology. There is the accumulation of T lymphocytes beneath the epithelium of the oral mucosa and increase in the rate of differentiation of stratified squamous epithelium, causing hyperkeratosis and erythema with or without ulceration.  Clinically it was originally classified into six forms: Reticular, plaque, papular, bullous, atrophic, ulcerative . Role of Candida in lichen planus is still unclear.
| Role of Candida in Potentially Malignant Oral Disorders|| |
Studies on the association of Candida and leukoplakia date back to 1970s. There is a longstanding discussion whether Candida infection is a cause of leukoplakia or if it is a superimposed infection in a preexisting lesion. Leukoplakia on clinical ground that were histologically chronic hyperplastic candidiasis showed a higher rate of malignant transformation on follow-up.  Animal studies have shown that Candida can cause epithelial hyperplasia and cellular atypia. It has been shown that, upon treatment, nonhomogeneous Candida infected leukoplakia convert into a homogeneous lesion, and some lesions even regressed. 
Leukoplakia with candidal infection has a higher rate of malignant transformation than uninfected leukoplakia. The ability of C. albicans to colonize, penetrate, and damage host tissues depend on the imbalance between C. albicans virulence factors and host defenses, often due to specific defects in the immune system.  Several cell surface proteins called adhesins recognizing host molecules are identified. They adhere to the cell surface and then phenotypic switching from the yeast form to hyphae form occurs by two mechanisms as described above.
Candida can then produce carcinogenic compounds, like nitrosamines, N-nitrosobenzylmethylamine. Strains with high nitrosation potential were isolated from lesions with more advanced precancerous changes. The yeast cells in such cases extends from the mucosal surface to the deeper epithelial cell layers representing transport and deposition of precursors like nitrosamines to deeper layers. This showed that certain strains of C. albicans play a key role in the development of dysplasia. 
Carcinogenic compounds then can bind with DNA to form adducts causing miscoding or irregularities with DNA replication. Thus results in oncogene formation and initiating cancer development. , All these findings suggest that there is a strong association between leukoplakia and Candida sp.
Few studies relating Candida and OSMF showed significantly high oral yeast carriage when compared to normal.  Candida dubliniensis was isolated from oral rinse samples in some studies.  In the case of lichen planus significant results are not obtained. 
| Conclusion|| |
Although Candida spp. particularly C. albicans has been considered an etiologic factor for potentially malignant disorders, the pathogenesis is not clearly understood and is still a field under extensive research. C. albicans being a normal commensal in the oral cavity, its presence alone cannot be related to the etiology of PMD. On the other hand, its frequent presence in advanced leukoplakia cases and ability to produce potent carcinogens should also be considered. Thus, PMD lesions associated with Candida should be treated with great caution as its shows a higher rate of malignant transformation.
| References|| |
Petersen PE. Oral cancer prevention and control - The approach of the World Health Organization. Oral Oncol 2009;45:454-60.
Silverman S Jr, Gorsky M, Lozada F. Oral leukoplakia and malignant transformation. A follow-up study of 257 patients. Cancer 1984;53:563-8.
Warnakulasuriya S, Johnson NW, van der Waal I. Nomenclature and classification of potentially malignant disorders of the oral mucosa. J Oral Pathol Med 2007;36:575-80.
Amagasa T, Yamashiro M, Uzawa N. Oral premalignant lesions: From a clinical perspective. Int J Clin Oncol 2011;16:5-14.
Bouquot NDA. Oral and Maxillofacial Pathology. 2 nd
ed. Philadelphia: Saunders Elsevier; 2002. p. 5055-08.
Bouza E, Muñoz P. Epidemiology of candidemia in intensive care units. Int J Antimicrob Agents 2008;32 Suppl 2:S87-91.
Marol S, Yücesoy M. Molecular epidemiology of Candida species isolated from clinical specimens of intensive care unit patients. Mycoses 2008;51:40-9.
Martin DS, Jones CP. Further Studies on the Practical Classification of the Monilias. J Bacteriol 1940;39:609-30.
Lim DV. Microbiology. 2 nd
ed. the University of Michigan: WBC/McGraw-Hill; 1998, 2008. [E-book].
McCool L. The Discovery and Naming of Candida albicans. [Reprint]. Available from: http://www.antimicrobe.org. [Last accessed on 2008 May 12]
Sudbery PE. Growth of Candida albicans hyphae. Nat Rev Microbiol 2011 16;9:737-48.
Phan QT, Myers CL, Fu Y, Sheppard DC, Yeaman MR, Welch WH, et al. Als3 is a Candida albicans invasin that binds to cadherins and induces endocytosis by host cells. PLoS Biol 2007;5:e64.
Kramer IR, Lucas RB, Pindborg JJ, Sobin LH. Definition of leukoplakia and related lesions: An aid to studies on oral precancer. Oral Surg Oral Med Oral Pathol 1978;46:518-39.
Pindborg JJ, Reichart PA, Smith CJ, Van Der Waal I. Histological Typing of the Cancer and Precancer of Oral Mucosa. 2 nd
ed. Tokyo: Springer; 1997.
Sudarshan R, Annigeri RG, Sree Vijayabala G. Pathogenesis of oral submucous fibrosis: The past and current concept. International Journal of Oral and Maxillofacial Pathology 2012;3:27-36.
Sudarshan R, Annigeri RG, Sree Vijayabala G. Pathogenesis of oral submucous fibrosis. Int J Oral Maxillofac Pathol 2012;3:27-36.
Epstein JB, Wan LS, Gorsky M, Zhang L. Oral lichen planus: Progress in understanding its malignant potential and the implications for clinical management. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2003;96:32-7.
Russell C, Jones JH. The histology of prolonged candidal infection of the rat's tongue. J Oral Pathol 1975;4:330-9.
Cawson RA, Binnie WH. Candida, leukoplakia and carcinoma: A possible relationship. In: Mackenzie I, Dabelsteen E, Squier CA, editors. Oral Premalignancy. Proceedings of the First Dows Symposium. Iowa: University of Iowa Press; 1980. p. 59-66.
Krogh P, Hald B, Holmstrup P. Possible mycological etiology of oral mucosal cancer: Catalytic potential of infecting Candida albicans and other yeasts in production of N-nitrosobenzylmethylamine. Carcinogenesis 1987;8:1543-8.
O'Grady JF, Reade PC. Candida albicans as a promoter of oral mucosal neoplasia. Carcinogenesis 1992;13:783-6.
Ariyawardana A, Panagoda GJ, Fernando HN, Ellepola AN, Tilakaratne WM, Samaranayake LP. Oral submucous fibrosis and oral yeast carriage-A case control study in Sri Lankan patients. Mycoses 2007;50:116-20.
Mehdipour M, Taghavi Zenouz A, Hekmatfar S, Adibpour M, Bahramian A, Khorshidi R. Prevalence of Candida species in erosive oral lichen planus. J Dent Res Dent Clin Dent Prospects 2010;4:14-6.
|This article has been cited by|
||The Mycobiome: Cancer Pathogenesis, Diagnosis, and Therapy
| ||Ahmed Gamal, Mohammed Elshaer, Mayyadah Alabdely, Ahmed Kadry, Thomas S. McCormick, Mahmoud Ghannoum |
| ||Cancers. 2022; 14(12): 2875 |
|[Pubmed] | [DOI]|
||Single-Cell RNA Sequencing Analysis for Oncogenic Mechanisms Underlying Oral Squamous Cell Carcinoma Carcinogenesis with Candida albicans Infection
| ||Yi-Ping Hsieh, Yu-Hsueh Wu, Siao-Muk Cheng, Fang-Kuei Lin, Daw-Yang Hwang, Shih-Sheng Jiang, Ken-Chung Chen, Meng-Yen Chen, Wei-Fan Chiang, Ko-Jiunn Liu, Nam Cong-Nhat Huynh, Wen-Tsung Huang, Tze-Ta Huang |
| ||International Journal of Molecular Sciences. 2022; 23(9): 4833 |
|[Pubmed] | [DOI]|
||Evaluation of the Distribution of Candida Species in Patients with Dysplastic and Nondysplastic Oral Lichen Planus Lesions
| ||Fahimeh Rezazadeh, Morteza Beirami, Zahra Zareshahrabadi, Hossein Sedarat, Kamiar Zomorodian, Luca Fiorillo |
| ||BioMed Research International. 2022; 2022: 1 |
|[Pubmed] | [DOI]|
||Proto-Oncogenes and Cell Cycle Gene Expression in Normal and Neoplastic Oral Epithelial Cells Stimulated With Soluble Factors From Single and Dual Biofilms of Candida albicans and Staphylococcus aureus
| ||María Isabel Amaya Arbeláez, Ana Carolina Alves de Paula e Silva, Geovana Navegante, Valeria Valente, Paula Aboud Barbugli, Carlos Eduardo Vergani |
| ||Frontiers in Cellular and Infection Microbiology. 2021; 11 |
|[Pubmed] | [DOI]|
||Candida albicans and Oral Carcinogenesis. A Brief Review
| ||Michele Di Cosola, Angela Pia Cazzolla, Ioannis Alexandros Charitos, Andrea Ballini, Francesco Inchingolo, Luigi Santacroce |
| ||Journal of Fungi. 2021; 7(6): 476 |
|[Pubmed] | [DOI]|
||Higher Number of EBI3 Cells in Mucosal Chronic Hyperplastic Candidiasis May Serve to Regulate IL-17-Producing Cells
| ||Ailish Williams, Helen Rogers, David Williams, Xiao-Qing Wei, Damian Farnell, Sue Wozniak, Adam Jones |
| ||Journal of Fungi. 2021; 7(7): 533 |
|[Pubmed] | [DOI]|
||Oral Potentially Malignant Disorders: A Proposal of a Novel Disease Concept in Japan
| ||Daisuke ITO, Hatsuhiko MAEDA |
| ||Journal of Japanese Society of Oral Medicine. 2020; 26(1): 1 |
|[Pubmed] | [DOI]|