<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Boss MK</submitter><funding>NCATS NIH HHS</funding><funding>Boehringer Ingelheim</funding><funding>College of Veterinary Medicine and Biomedical Sciences, Colorado State University</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>1033704</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9868558</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Improving outcomes for oral squamous cell carcinoma (OSCC) patients has been hindered by a lack of effective predictive animal models. Spontaneously occurring canine OSCC could help fill this gap. The objective of this study was to characterize the immune landscape of canine OSCC to advance understanding of how dogs could serve as a surrogate for human OSCC.&lt;h4>Methods/results&lt;/h4>Canine OSCC contains a heterogenous tumor immune microenvironment. CD3+ T cells were the predominant tumor infiltrating immune cell population; however, there was a wide range CD3+ T cell density across samples. The most common CD3+ T cell micro-anatomical distribution was defined as "pre-existing immunity", but the remaining 20% of tumors were characterized as "immunologically ignorant" or "</pubmed_abstract><journal>Frontiers in oncology</journal><pubmed_title>Canine oral squamous cell carcinoma as a spontaneous, translational model for radiation and immunology research.</pubmed_title><pmcid>PMC9868558</pmcid><funding_grant_id>K01 OD031809</funding_grant_id><funding_grant_id>K01 OD022982</funding_grant_id><funding_grant_id>K01 OD022982, L30 TR002126, K01 OD031809</funding_grant_id><funding_grant_id>L30 TR002126</funding_grant_id><pubmed_authors>Harrison LG</pubmed_authors><pubmed_authors>Gold A</pubmed_authors><pubmed_authors>Regan DP</pubmed_authors><pubmed_authors>Boss MK</pubmed_authors><pubmed_authors>Karam SD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Canine oral squamous cell carcinoma as a spontaneous, translational model for radiation and immunology research.</name><description>&lt;h4>Introduction&lt;/h4>Improving outcomes for oral squamous cell carcinoma (OSCC) patients has been hindered by a lack of effective predictive animal models. Spontaneously occurring canine OSCC could help fill this gap. The objective of this study was to characterize the immune landscape of canine OSCC to advance understanding of how dogs could serve as a surrogate for human OSCC.&lt;h4>Methods/results&lt;/h4>Canine OSCC contains a heterogenous tumor immune microenvironment. CD3+ T cells were the predominant tumor infiltrating immune cell population; however, there was a wide range CD3+ T cell density across samples. The most common CD3+ T cell micro-anatomical distribution was defined as "pre-existing immunity", but the remaining 20% of tumors were characterized as "immunologically ignorant" or "</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-07-14T21:16:59.67Z</modification><creation>2025-04-06T11:11:50.536Z</creation></dates><accession>S-EPMC9868558</accession><cross_references><pubmed>36698398</pubmed><doi>10.3389/fonc.2022.1033704</doi></cross_references></HashMap>