Global transcriptional response of oral squamous cell carcinoma cell lines to health-associated oral bacteria - an in vitro study
dc.creator | Baraniya, Divyashri | |
dc.creator | Chitrala, Kumaraswamy naidu | |
dc.creator | Al-hebshi, Nezar | |
dc.date.accessioned | 2024-01-23T15:32:21Z | |
dc.date.available | 2024-01-23T15:32:21Z | |
dc.date.issued | 2022-05-16 | |
dc.identifier.citation | Divyashri Baraniya, Kumaraswamy Naidu Chitrala & Nezar Noor Al-Hebshi (2022) Global transcriptional response of oral squamous cell carcinoma cell lines to health-associated oral bacteria - an in vitro study, Journal of Oral Microbiology, 14:1, DOI: 10.1080/20002297.2022.2073866 | |
dc.identifier.issn | 2000-2297 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12613/9634 | |
dc.description.abstract | 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. | |
dc.format.extent | 10 pages | |
dc.language | English | |
dc.language.iso | eng | |
dc.relation.ispartof | Faculty/ Researcher Works | |
dc.relation.haspart | Journal of Oral Microbiology, Vol. 14, Iss. 1 | |
dc.relation.isreferencedby | Taylor and Francis Group | |
dc.rights | Attribution CC BY | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Mouth neoplasms | |
dc.subject | Cell line | |
dc.subject | Bacteria | |
dc.subject | Microarray analysis | |
dc.subject | Transcriptome | |
dc.title | Global transcriptional response of oral squamous cell carcinoma cell lines to health-associated oral bacteria - an in vitro study | |
dc.type | Text | |
dc.type.genre | Journal article | |
dc.contributor.group | Oral Microbiome Research Laboratory (Temple University) | |
dc.contributor.group | Fels Cancer Institute for Personalized Medicine (Temple University) | |
dc.contributor.group | Fox Chase Cancer Center (Temple University) | |
dc.relation.doi | http://dx.doi.org/10.1080/20002297.2022.2073866 | |
dc.ada.note | For Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu | |
dc.description.schoolcollege | Kornberg School of Dentistry | |
dc.description.schoolcollege | Lewis Katz School of Medicine | |
dc.creator.orcid | Baraniya|0000-0002-6231-131X | |
dc.creator.orcid | Chitrala|0000-0003-0663-9529 | |
dc.creator.orcid | Al-Hebshi|0000-0003-1841-9304 | |
dc.temple.creator | Baraniya, Divyashri | |
dc.temple.creator | Chitrala, Kumaraswamy Naidu | |
dc.temple.creator | Al-Hebshi, Nezar Noor | |
refterms.dateFOA | 2024-01-23T15:32:21Z |