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Candida albicans Enhances the Progression of Oral Squamous Cell Carcinoma In Vitro and In Vivo

Oral squamous cell carcinoma (OSCC) is associated with oral Candida albicans infection, although it is unclear whether the fungus promotes the genesis and progression of OSCC or whether cancer facilitates fungal growth. In this study, we investigated whether C. albicans can potentiate OSCC tumor dev...

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Detalles Bibliográficos
Autores principales: Vadovics, Máté, Ho, Jemima, Igaz, Nóra, Alföldi, Róbert, Rakk, Dávid, Veres, Éva, Szücs, Balázs, Horváth, Márton, Tóth, Renáta, Szücs, Attila, Csibi, Andrea, Horváth, Péter, Tiszlavicz, László, Vágvölgyi, Csaba, Nosanchuk, Joshua D., Szekeres, András, Kiricsi, Mónika, Henley-Smith, Rhonda, Moyes, David L., Thavaraj, Selvam, Brown, Rhys, Puskás, László G., Naglik, Julian R., Gácser, Attila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725587/
https://www.ncbi.nlm.nih.gov/pubmed/35089096
http://dx.doi.org/10.1128/mBio.03144-21
Descripción
Sumario:Oral squamous cell carcinoma (OSCC) is associated with oral Candida albicans infection, although it is unclear whether the fungus promotes the genesis and progression of OSCC or whether cancer facilitates fungal growth. In this study, we investigated whether C. albicans can potentiate OSCC tumor development and progression. In vitro, the presence of live C. albicans, but not Candida parapsilosis, enhanced the progression of OSCC by stimulating the production of matrix metalloproteinases, oncometabolites, protumor signaling pathways, and overexpression of prognostic marker genes associated with metastatic events. C. albicans also upregulated oncogenes in nonmalignant cells. Using a newly established xenograft in vivo mouse model to investigate OSCC-C. albicans interactions, oral candidiasis enhanced the progression of OSCC through inflammation and induced the overexpression of metastatic genes and significant changes in markers of the epithelial-mesenchymal transition. Finally, using the 4-nitroquinoline 1-oxide (4NQO) murine model, we directly correlate these in vitro and short-term in vivo findings with the progression of oncogenesis over the long term. Taken together, these data indicate that C. albicans upregulates oncogenes, potentiates a premalignant phenotype, and is involved in early and late stages of malignant promotion and progression of oral cancer.