{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,25]],"date-time":"2026-09-25T03:04:13Z","timestamp":1790305453806,"version":"4.1.0"},"reference-count":78,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2026,2,22]],"date-time":"2026-02-22T00:00:00Z","timestamp":1771718400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,2,22]],"date-time":"2026-02-22T00:00:00Z","timestamp":1771718400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"DOI":"10.13039\/100018065","name":"EveryCat Health Foundation","doi-asserted-by":"publisher","award":["W21"],"award-info":[{"award-number":["W21"]}],"id":[{"id":"10.13039\/100018065","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000051","name":"National Human Genome Research Institute","doi-asserted-by":"publisher","award":["R00HG007940"],"award-info":[{"award-number":["R00HG007940"]}],"id":[{"id":"10.13039\/100000051","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000054","name":"National Cancer Institute","doi-asserted-by":"publisher","award":["K22CA188163"],"award-info":[{"award-number":["K22CA188163"]}],"id":[{"id":"10.13039\/100000054","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100014571","name":"Alvin J. 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In humans, despite surgery, radiation therapy, and chemotherapy, 1\/3 of patients develop loco\u2010regional recurrence within 5\u2009years. FOSCC has commonly been proposed as a model for HNSCC since FOSCC is a spontaneous model and exhibits similar biologic behaviour, treatment course, and outcome to the human disease. The objective of this study was to identify genetic similarities and differences with HNSCC, therapeutic targets, and possible causes of FOSCC through whole exome sequencing. Thirty\u2010six matched normal FOSCC tumours and three matched normal chronic gingivostomatitis lesions were sequenced with a previously validated custom Roche Nimblegen exome reagent, based on the Felis_catus_9.0 genome assembly, covering 35.7\u2009Mb. The exome libraries were pooled and sequenced on the Illumina Novaseq6000 as 2\u2009\u00d7\u2009150\u2009bp reads. The data was analysed with the McDonnell Genome Institute's (MGI) cancer informatics pipelines, namely the Genome Modelling System (GMS), which was adapted to the feline genome.\n                    <jats:italic>TP53<\/jats:italic>\n                    harboured consequential variants in 71% of the FOSCC tumours and was the most commonly mutated gene. Consequential variants in\n                    <jats:italic>TTN<\/jats:italic>\n                    were seen in 18% tumours and consequential variants in\n                    <jats:italic>FSIP2, LRP1B, RYR2<\/jats:italic>\n                    were seen 9% of tumours. Genes with highly recurrent copy number variants (CNVs) included\n                    <jats:italic>CKDN2A, PTEN,<\/jats:italic>\n                    and\n                    <jats:italic>MYC<\/jats:italic>\n                    . TMB was very low, 0\u20131.6 (mean 0.66). Six cats had a history of chronic gingivostomatitis for years before the diagnosis of FOSCC. Despite the low TMB, the genomic landscape of FOSCC parallels HPV\u2010negative HNSCC. Aside from\n                    <jats:italic>TP53,<\/jats:italic>\n                    recurrent small\u2010scale mutations in FOSCC were uncommon, but recurrent CNVs were common. FOSCC is a genetically and clinically heterogenous cancer. A multifactorial cause is suspected. Chronic gingivostomatitis, immunosuppression, and\/or viral infection may be associated with FOSCC in young cats.\n                  <\/jats:p>","DOI":"10.1111\/vco.70054","type":"journal-article","created":{"date-parts":[[2026,2,23]],"date-time":"2026-02-23T04:26:14Z","timestamp":1771820774000},"page":"300-312","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":2,"title":["Whole Exome Sequencing of Feline Oral Squamous Cell Carcinoma Reveals Genomic Parallels With Human Head and Neck Squamous Cell Carcinoma"],"prefix":"10.1111","volume":"24","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8164-7268","authenticated-orcid":false,"given":"Shirley","family":"Chu","sequence":"first","affiliation":[{"name":"Department of Veterinary Medicine and Surgery University of Missouri  Columbia Missouri 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