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Candida albicans Enhances the Progression of Oral Squamous Cell Carcinoma In Vitro and In Vivo.
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.
Affiliation
  • Vadovics M; Department of Microbiology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Ho J; Doctoral School of Biology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Igaz N; Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom.
  • Alföldi R; Doctoral School of Biology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Rakk D; Department of Biochemistry and Molecular Biology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Veres É; AstridBio Technologies Ltd., Szeged, Hungary.
  • Szücs B; Department of Microbiology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Horváth M; Doctoral School of Biology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Tóth R; Department of Microbiology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Szücs A; Doctoral School of Biology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Csibi A; Department of Microbiology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Horváth P; Department of Microbiology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Tiszlavicz L; Department of Microbiology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Vágvölgyi C; Department of Microbiology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Nosanchuk JD; Department of Microbiology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Szekeres A; Synthetic and System Biology Unit, Biological Research Centre (BRC), Szeged, Hungary.
  • Kiricsi M; Department of Pathology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Henley-Smith R; Department of Microbiology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Moyes DL; Division of Infectious Diseases, Department of Medicine, Albert Einstein College of Medicine, Bronx, New York, USA.
  • Thavaraj S; Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York, USA.
  • Brown R; Department of Microbiology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Puskás LG; Department of Biochemistry and Molecular Biology, University of Szegedgrid.9008.1, Szeged, Hungary.
  • Naglik JR; King's Health Partners, Head and Neck Cancer Biobank, Guy's & St Thomas' NHS Foundation Trust, London, United Kingdom.
  • Gácser A; Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, United Kingdom.
mBio ; 13(1): e0314421, 2021 02 22.
Article in En | MEDLINE | ID: mdl-35089096
ABSTRACT
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. IMPORTANCE Oral squamous cell carcinoma (OSCC) is a serious health issue worldwide that accounts for 2% to 4% of all cancer cases. Previous studies have revealed a higher yeast carriage and diversity in oral cancer patients than in healthy individuals. Furthermore, fungal colonization in the oral cavity bearing OSCC is higher on the neoplastic epithelial surface than on adjacent healthy surfaces, indicating a positive association between oral yeast carriage and epithelial carcinoma. In addition to this, there is strong evidence supporting the idea that Candida contributes to carcinogenesis events in the oral cavity. Here, we show that an increase in Candida albicans burden promotes an oncogenic phenotype in the oral cavity.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Candidiasis, Oral / Mouth Neoplasms / Carcinoma, Squamous Cell / Head and Neck Neoplasms Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: MBio Year: 2021 Document type: Article Affiliation country: Hungary

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Candidiasis, Oral / Mouth Neoplasms / Carcinoma, Squamous Cell / Head and Neck Neoplasms Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: MBio Year: 2021 Document type: Article Affiliation country: Hungary