Is Candida albicans an opportunistic oncogenic pathogen?
[...]although correlative, these studies have undoubtedly demonstrated increased Candida colonization, as the epithelial lining of the oral mucosa alters from normal to dysplastic epithelium [5,6]. [...]Candida recovery from the oral cavity of patients with oral epithelial dysplasia [5] and the pres...
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Published in: | PLoS pathogens Vol. 18; no. 4; p. e1010413 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
Public Library of Science
14-04-2022
Public Library of Science (PLoS) |
Subjects: | |
Online Access: | Get full text |
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Summary: | [...]although correlative, these studies have undoubtedly demonstrated increased Candida colonization, as the epithelial lining of the oral mucosa alters from normal to dysplastic epithelium [5,6]. [...]Candida recovery from the oral cavity of patients with oral epithelial dysplasia [5] and the presence of hyphae in tissue sections [6] correlated with the severity of dysplastic changes. [...]Candida was shown to display increased metabolic activity and acetaldehyde production in oral cancer compared to healthy controls, reinforcing its potential carcinogenic role [19]. ADH1, alcohol dehydrogenase 1; EGFR, epidermal growth factor receptor; G-CSF, granulocyte colony-stimulating factor; IFNγ, interferon gamma; IL, interleukin; NFκΒ, nuclear factor kappa B; OSCC, oral squamous cell carcinoma; ROS, reactive oxygen species; Th, T helper. https://doi.org/10.1371/journal.ppat.1010413.g001 On the other hand, some studies described C. albicans as a promoter or “facilitator” of cancer development, rather than initiators; in one study, oral inoculation with C. albicans or administration of the carcinogen 4NQO [21] failed to cause dysplastic changes in animal models; however, in combination, oral epithelial dysplasia occured, indicating that C. albicans may have promoted dysplastic changes [21–23]. [...]other cytokines of the Th17 family, such as IL-23, promote angiogenesis and tumor growth [29]. [...]type 17 responses antagonize IL-12 and interferon gamma (IFNγ), both of which are crucial in Th1-type antitumor immune responses [29]. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 The authors have declared that no competing interests exist. |
ISSN: | 1553-7374 1553-7366 1553-7374 |
DOI: | 10.1371/journal.ppat.1010413 |