<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gao S</submitter><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Institute of Dental and Craniofacial Research</funding><funding>NIDCR NIH HHS</funding><funding>National Science Foundation of China | National Natural Science Foundation of China-Yunnan Joint Fund</funding><funding>NIGMS NIH HHS</funding><pagination>433-444</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8329259</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>125(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The effect of Porphyromonas gingivalis (Pg) infection on oesophageal squamous cell carcinoma (ESCC) prognosis, chemotherapeutic efficacy, and oesophageal cancer cell apoptosis resistance and proliferation remain poorly understood.&lt;h4>Methods&lt;/h4>Clinicopathological data from 312 ESCC oesophagectomy patients, along with the computed tomography imaging results and longitudinal cancerous tissue samples from a patient subset (n = 85) who received neoadjuvant chemotherapy (NACT), were analysed. Comparison of overall survival and response rate to NACT between Pg-infected and Pg-uninfected patients was made by multivariate Cox analysis and Response Evaluation Criteria in Solid Tumours v.1.1 criteria. The influence of Pg on cell proliferation and drug-induced apoptosis was examined in ESCC patients and validated in vitro and in vivo.&lt;h4>Results&lt;/h4>The 5-year overall survival was lower in Pg-positive patients, and infection was associated with multiple clinicopathological factors and pathologic tumour, node, metastasis stage. Of the 85 patients who received NACT, Pg infection was associated with a lower response rate and 5-year overall survival. Infection with Pg resulted in apoptosis resistance in ESCC and promoted ESCC cell viability, which was confirmed in longitudinal cancerous tissue samples. Pg-induced apoptosis resistance was dependent on fimbriae and STAT3.&lt;h4>Conclusions&lt;/h4>Pg infection is associated with a worse ESCC prognosis, reduced chemotherapy efficacy, and can potentiate the aggressive behaviour of ESCC cells.</pubmed_abstract><journal>British journal of cancer</journal><pubmed_title>Porphyromonas gingivalis infection exacerbates oesophageal cancer and promotes resistance to neoadjuvant chemotherapy.</pubmed_title><pmcid>PMC8329259</pmcid><funding_grant_id>R01 DE026727</funding_grant_id><funding_grant_id>R01 DE026963</funding_grant_id><funding_grant_id>DE 026Lamont727</funding_grant_id><funding_grant_id>P20 GM125504</funding_grant_id><funding_grant_id>GS 81472234</funding_grant_id><funding_grant_id>DE 0Lamont26727</funding_grant_id><funding_grant_id>DE 026727</funding_grant_id><pubmed_authors>Liang S</pubmed_authors><pubmed_authors>Liu K</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Gu Z</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Lamont RJ</pubmed_authors><pubmed_authors>Mohammed M</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Yakoumatos L</pubmed_authors><pubmed_authors>Lu L</pubmed_authors><pubmed_authors>Scott DA</pubmed_authors><pubmed_authors>Ren J</pubmed_authors><pubmed_authors>Zhou F</pubmed_authors><pubmed_authors>Yuan X</pubmed_authors><pubmed_authors>Gao S</pubmed_authors><pubmed_authors>Duan X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Porphyromonas gingivalis infection exacerbates oesophageal cancer and promotes resistance to neoadjuvant chemotherapy.</name><description>&lt;h4>Background&lt;/h4>The effect of Porphyromonas gingivalis (Pg) infection on oesophageal squamous cell carcinoma (ESCC) prognosis, chemotherapeutic efficacy, and oesophageal cancer cell apoptosis resistance and proliferation remain poorly understood.&lt;h4>Methods&lt;/h4>Clinicopathological data from 312 ESCC oesophagectomy patients, along with the computed tomography imaging results and longitudinal cancerous tissue samples from a patient subset (n = 85) who received neoadjuvant chemotherapy (NACT), were analysed. Comparison of overall survival and response rate to NACT between Pg-infected and Pg-uninfected patients was made by multivariate Cox analysis and Response Evaluation Criteria in Solid Tumours v.1.1 criteria. The influence of Pg on cell proliferation and drug-induced apoptosis was examined in ESCC patients and validated in vitro and in vivo.&lt;h4>Results&lt;/h4>The 5-year overall survival was lower in Pg-positive patients, and infection was associated with multiple clinicopathological factors and pathologic tumour, node, metastasis stage. Of the 85 patients who received NACT, Pg infection was associated with a lower response rate and 5-year overall survival. Infection with Pg resulted in apoptosis resistance in ESCC and promoted ESCC cell viability, which was confirmed in longitudinal cancerous tissue samples. Pg-induced apoptosis resistance was dependent on fimbriae and STAT3.&lt;h4>Conclusions&lt;/h4>Pg infection is associated with a worse ESCC prognosis, reduced chemotherapy efficacy, and can potentiate the aggressive behaviour of ESCC cells.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Aug</publication><modification>2025-04-05T10:04:06.629Z</modification><creation>2025-04-05T10:04:06.629Z</creation></dates><accession>S-EPMC8329259</accession><cross_references><pubmed>33981017</pubmed><doi>10.1038/s41416-021-01419-5</doi></cross_references></HashMap>