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Global transcriptional response of oral squamous cell carcinoma cell lines to health-associated oral bacteria - an in vitro study

BACKGROUND: We have recently demonstrated that health-associated oral bacteria Streptococcus mitis, Neisseria flavescens, and Haemophilus parainfluenzae induce cytotoxicity in oral squamous cell carcinoma (OSCC) cell lines and downregulate CD36, a cancer-assocaited gene. AIM: To explore the effect o...

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Detalles Bibliográficos
Autores principales: Baraniya, Divyashri, Chitrala, Kumaraswamy Naidu, Al-Hebshi, Nezar Noor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116255/
https://www.ncbi.nlm.nih.gov/pubmed/35600164
http://dx.doi.org/10.1080/20002297.2022.2073866
Descripción
Sumario:BACKGROUND: We have recently demonstrated that health-associated oral bacteria Streptococcus mitis, Neisseria flavescens, and Haemophilus parainfluenzae induce cytotoxicity in oral squamous cell carcinoma (OSCC) cell lines and downregulate CD36, a cancer-assocaited gene. AIM: To explore the effect of these three species on global transcriptome of OSCC cell lines. METHODS: Gene expression of cell lines CAL27, SCC4 and SCC25 cocultured with the test species was assessed with Clariom-S Human microarray. Porphyromonas gingivalis was included as a pathogenic control. Data were analyzed using Ingenuity Pathway Analysis. RESULTS: The results differed by species and cell line. Overall, the transcriptional changes by S. mitis were predominantly anti-cancer including inhibition of HOTAIR regulatory pathway, JAK/Stat signaling, cyclins/cyclin-dependent kinases, and endothelin1 signaling. H. parainfluenzae and N. flavescens resulted in a mix of pro- and anti-cancer responses including activation of acute phase response, pro-inflammatory interleukins signaling, TREM-1 signaling, and tumor microenvironment pathway; but downregulation of cell cycle by inhibition of cyclins and cyclin-dependent kinases. P. gingivalis had a predominantly pro-cancer effect limited to SCC4, including upregulation of inflammatory pathways, phospholipases and PI3K signaling. CONCLUSION: These findings provide a new insight into the role of commensal oral bacteria in OSCC. Animal studies are required to further explore them.