<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang C</submitter><funding>the Modern Dental Laboratory/HKU Endowment Fund to L.J. Jin</funding><funding>the Hong Kong Research Grants Council</funding><pagination>5728</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9146424</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(10)</volume><pubmed_abstract>&lt;i>Porphyromonas gingivalis&lt;/i> as the keystone periodontopathogen plays a critical role in the pathogenesis of periodontitis, and crucially accounts for inflammatory comorbidities such as cardiovascular disease and Alzheimer's disease. We recently identified the existence of &lt;i>P. gingivalis&lt;/i> persisters and revealed the unforeseen perturbation of innate response in human gingival epithelial cells (HGECs) due to these noxious persisters. Herein, RNA sequencing revealed how &lt;i>P. gingivalis&lt;/i> persisters affected the expression profile of cytokine genes and related signaling pathways in HGECs. Results showed that metronidazole-treated &lt;i>P. gingivalis&lt;/i> persisters (M-PgPs) impaired the innate host defense of HGECs, in a similar fashion to &lt;i>P. gingivalis&lt;/i>. Notably, over one thousa</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>RNA Sequencing Reveals the Upregulation of FOXO Signaling Pathway in &lt;i>Porphyromonas gingivalis&lt;/i> Persister-Treated Human Gingival Epithelial Cells.</pubmed_title><pmcid>PMC9146424</pmcid><funding_grant_id>Nil</funding_grant_id><funding_grant_id>17122918, 17119819</funding_grant_id><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Cheng T</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Jin L</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA Sequencing Reveals the Upregulation of FOXO Signaling Pathway in &lt;i>Porphyromonas gingivalis&lt;/i> Persister-Treated Human Gingival Epithelial Cells.</name><description>&lt;i>Porphyromonas gingivalis&lt;/i> as the keystone periodontopathogen plays a critical role in the pathogenesis of periodontitis, and crucially accounts for inflammatory comorbidities such as cardiovascular disease and Alzheimer's disease. We recently identified the existence of &lt;i>P. gingivalis&lt;/i> persisters and revealed the unforeseen perturbation of innate response in human gingival epithelial cells (HGECs) due to these noxious persisters. Herein, RNA sequencing revealed how &lt;i>P. gingivalis&lt;/i> persisters affected the expression profile of cytokine genes and related signaling pathways in HGECs. Results showed that metronidazole-treated &lt;i>P. gingivalis&lt;/i> persisters (M-PgPs) impaired the innate host defense of HGECs, in a similar fashion to &lt;i>P. gingivalis&lt;/i>. Notably, over one thousa</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-05-29T14:36:24.83Z</modification><creation>2025-02-19T02:16:20.636Z</creation></dates><accession>S-EPMC9146424</accession><cross_references><pubmed>35628542</pubmed><doi>10.3390/ijms23105728</doi></cross_references></HashMap>