<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE174nnn/GSE174160/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE174160</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>SFPQ rescues F508del-CFTR expression and function in cystic fibrosis bronchial epithelial cells</name><description>Here, we investigated the role of SFPQ in the regulation of expression and function of F508del-CFTR in CF lung epithelial cells. We find that the expression of SFPQ is reduced in F508del-CFTR CF epithelial cells compared to WT-CFTR control cells. Interestingly, the overexpression of SFPQ in CF cells increases the expression as well as rescues the function of F508del­CFTR. Further, comprehensive transcriptome analyses indicate that SFPQ plays a key role in activating the mutant F508del-CFTR by modulating several cellular signaling pathways. This is the first report on the role of SFPQ in the regulation of expression and function of F508del-CFTR in CF lung disease.</description><dates><publication>2026/04/21</publication></dates><accession>GSE174160</accession><cross_references><GSM>GSM5288125</GSM><GSM>GSM5288126</GSM><GSM>GSM5288130</GSM><GSM>GSM5288127</GSM><GSM>GSM5288128</GSM><GSM>GSM5288129</GSM><GPL>16791</GPL><SRA>SRP319174</SRA><GSE>174160</GSE><taxon>Homo sapiens</taxon><PMID>[34404863]</PMID></cross_references></HashMap>