{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,7]],"date-time":"2025-11-07T09:33:43Z","timestamp":1762508023441,"version":"3.41.2"},"reference-count":39,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2020,4,18]],"date-time":"2020-04-18T00:00:00Z","timestamp":1587168000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["The Journal of Gene Medicine"],"published-print":{"date-parts":[[2020,7]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Head and neck squamous cell carcinoma (HNSCC) has attracted the attention of researchers as a result of its high incidence around the world. This malignancy occurs in the oral cavity, pharynx and larynx in most cases. A number of lncRNAs have been revealed to regulate the malignant neoplasia of several cancers. Nevertheless, the effects of lncRNA LINC00467 in HNSCC have not yet been reported.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>The expression of LINC00467, miR\u2010299\u20105p and ubiquitin specific protease\u201048 (USP48) in HNSCC cells was quantified by a quantitative reverse transcriptase\u2010polymerase chain reaction. The influences of LINC00467 deficiency on HNSCC progression were reflected by cell counting kit\u20108, colony formation, ethynyl\u20102\u2010deoxyuridine, wound healing and western blot assays. RIP and luciferase reporter assays were conducted to confirm the interaction among LINC00467, miR\u2010299\u20105p and USP48.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>LINC00467 was considerably upregulated in HNSCC cells, and an absence of LINC00467 suppressed cell growth, cell migration and the epithelial\u2013mesenchymal process in HNSCC. In addition, miR\u2010299\u20105p expression was notably downregulated in HNSCC cells, and miR\u2010299\u20105p could bind with LINC00467. Furthermore, USP48 was conspicuously overexpressed in HNSCC cells and capable of binding with miR\u2010299\u20105p. LINC00467 could upregulate USP48 expression via sponging miR\u2010299\u20105p. Finally, rescue assays proved that USP48 overexpression could compensate for the suppressive effects on HNSCC progression mediated by LINC00467 deficiency.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>LINC00467 enhances HNSCC progression by serving as a sponge of miR\u2010299\u20105p to increase USP48 expression.<\/jats:p><\/jats:sec>","DOI":"10.1002\/jgm.3184","type":"journal-article","created":{"date-parts":[[2020,3,11]],"date-time":"2020-03-11T10:02:17Z","timestamp":1583920937000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":18,"title":["LINC00467 enhances head and neck squamous cell carcinoma progression and the epithelial\u2013mesenchymal transition process via miR\u2010299\u20105p\/ubiquitin specific protease\u201048 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