<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu L</submitter><funding>Beijing Jingjian Pathology Development Foundation</funding><funding>the Natural Science Foundation of Shandong Province</funding><funding>the National Natural Science Foundation of China</funding><pagination>1481</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11610093</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Tongue squamous cell carcinoma (TSCC) is one of the most common malignant tumors with high mortality and poor prognosis. Its incidence rate is increasing gradually. Tumor necrosis factor receptor-associated factor interacting protein (TRAIP), as a factor related to several tumors, reveals that its gene expression is different between normal tissue and primary tumor of head and neck squamous cell carcinoma using bioinformatics analysis.&lt;h4>Method&lt;/h4>In our study, TCGA database, immunohistochemistry, proliferation assay, colony formation, wound healing assay, Transwell, cell cycle analysis and tumor xenografts model were used to determine the expression and functions of TRAIP in TSCC.&lt;h4>Result&lt;/h4>We found that TRAIP may promote the proliferation, migration and invasion </pubmed_abstract><journal>BMC cancer</journal><pubmed_title>TRAIP enhances progression of tongue squamous cell carcinoma through EMT and Wnt/β-catenin signaling by interacting with DDX39A.</pubmed_title><pmcid>PMC11610093</pmcid><funding_grant_id>No.81672606</funding_grant_id><funding_grant_id>JJlXA2022-008</funding_grant_id><funding_grant_id>ZR2022MH206</funding_grant_id><pubmed_authors>Song L</pubmed_authors><pubmed_authors>Zheng Y</pubmed_authors><pubmed_authors>Wang P</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Qi H</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Xing X</pubmed_authors><pubmed_authors>Guo C</pubmed_authors></additional><is_claimable>false</is_claimable><name>TRAIP enhances progression of tongue squamous cell carcinoma through EMT and Wnt/β-catenin signaling by interacting with DDX39A.</name><description>&lt;h4>Background&lt;/h4>Tongue squamous cell carcinoma (TSCC) is one of the most common malignant tumors with high mortality and poor prognosis. Its incidence rate is increasing gradually. Tumor necrosis factor receptor-associated factor interacting protein (TRAIP), as a factor related to several tumors, reveals that its gene expression is different between normal tissue and primary tumor of head and neck squamous cell carcinoma using bioinformatics analysis.&lt;h4>Method&lt;/h4>In our study, TCGA database, immunohistochemistry, proliferation assay, colony formation, wound healing assay, Transwell, cell cycle analysis and tumor xenografts model were used to determine the expression and functions of TRAIP in TSCC.&lt;h4>Result&lt;/h4>We found that TRAIP may promote the proliferation, migration and invasion </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2025-04-04T02:20:07.377Z</modification><creation>2025-04-04T02:20:07.377Z</creation></dates><accession>S-EPMC11610093</accession><cross_references><pubmed>39623306</pubmed><doi>10.1186/s12885-024-13130-8</doi></cross_references></HashMap>