{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:10:28Z","timestamp":1787015428290,"version":"build-2736575974"},"reference-count":79,"publisher":"Wiley","issue":"14","license":[{"start":{"date-parts":[[2024,7,19]],"date-time":"2024-07-19T00:00:00Z","timestamp":1721347200000},"content-version":"vor","delay-in-days":18,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2024,7,1]],"date-time":"2024-07-01T00:00:00Z","timestamp":1719792000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["J Cellular Molecular Medi"],"published-print":{"date-parts":[[2024,7]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    The pathogenesis of ankylosing spondylitis (AS) remains unclear, and while recent studies have implicated necroptosis in various autoimmune diseases, an investigation of its relationship with AS has not been reported. In this study, we utilized the Gene Expression Omnibus database to compare gene expressions between AS patients and healthy controls, identifying 18 differentially expressed necroptosis\u2010related genes (DENRGs), with 8 upregulated and 10 downregulated. Through the application of three machine learning algorithms\u2014least absolute shrinkage and selection operation, support vector machine\u2010recursive feature elimination and random forest\u2014two hub genes, FASLG and TARDBP, were pinpointed. These genes demonstrated high specificity and sensitivity for AS diagnosis, as evidenced by receiver operating characteristic curve analysis. These findings were further supported by external datasets and cellular experiments, which confirmed the downregulation of FASLG and upregulation of TARDBP in AS patients. Immune cell infiltration analysis suggested that CD4\n                    <jats:sup>+<\/jats:sup>\n                    T cells, CD8\n                    <jats:sup>+<\/jats:sup>\n                    T cells, NK cells and neutrophils may be associated with the development of AS. Notably, in the group with high FASLG expression, there was a significant infiltration of CD8\n                    <jats:sup>+<\/jats:sup>\n                    T cells, memory\u2010activated CD4\n                    <jats:sup>+<\/jats:sup>\n                    T cells and resting NK cells, with relatively less infiltration of memory\u2010resting CD4\n                    <jats:sup>+<\/jats:sup>\n                    T cells and neutrophils. Conversely, in the group with high TARDBP expression, there was enhanced infiltration of na\u00efve CD4\n                    <jats:sup>+<\/jats:sup>\n                    T cells and M0 macrophages, with a reduced presence of memory\u2010resting CD4\n                    <jats:sup>+<\/jats:sup>\n                    T cells. In summary, FASLG and TARDBP may contribute to AS pathogenesis by regulating the immune microenvironment and immune\u2010related signalling pathways. These findings offer new insights into the molecular mechanisms of AS and suggest potential new targets for therapeutic strategies.\n                  <\/jats:p>","DOI":"10.1111\/jcmm.18557","type":"journal-article","created":{"date-parts":[[2024,7,19]],"date-time":"2024-07-19T09:04:17Z","timestamp":1721379857000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Identification of necroptosis\u2010related genes in ankylosing spondylitis by bioinformatics and experimental validation"],"prefix":"10.1111","volume":"28","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8873-5172","authenticated-orcid":false,"given":"Pengfei","family":"Wen","sequence":"first","affiliation":[{"name":"Department of Joint Surgery, Honghui Hospital Xi'an Jiaotong University  Shaanxi China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yan","family":"Zhao","sequence":"additional","affiliation":[{"name":"Department of Laboratory, Honghui Hospital Xi'an Jiaotong University  Shaanxi China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mingyi","family":"Yang","sequence":"additional","affiliation":[{"name":"Department of Joint Surgery, Honghui Hospital Xi'an Jiaotong University  Shaanxi China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peng","family":"Yang","sequence":"additional","affiliation":[{"name":"Department of Joint Surgery, Honghui Hospital Xi'an Jiaotong University  Shaanxi China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0007-2498-1535","authenticated-orcid":false,"given":"Kai","family":"Nan","sequence":"additional","affiliation":[{"name":"Department of Joint Surgery, Honghui Hospital Xi'an Jiaotong University  Shaanxi China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lin","family":"Liu","sequence":"additional","affiliation":[{"name":"Department of Joint Surgery, Honghui Hospital Xi'an 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