<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/GSE107nnn/GSE107200/</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 array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE107200</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Regional heterogeneity in response of airway epithelial cells to cigarette smoke</name><description>To investigate the biochemical and genetic alterations that occur in response to cigarette smoke exposure among airway epithelial cells from different sites in the lungs, we performed microarray-based analysis using small airway epithelial cells (SAEC) and normal human bronchial epithelial cells (NHBE) following 24 h of cigarette smoke extract (CSE). In microarray-based analysis, the small airway showed higher susceptibility to CS compared to the large airway, such as enhanced expression of inflammatory-related pathways including the TNF signaling pathway. Among the TNF-related genes, PTGS2, also known as COX-2, showed the greatest difference in expression levels, with higher CSE-induced increments of both mRNA and protein expression in SAEC compared to NHBE.</description><dates><publication>2018/01/16</publication></dates><accession>GSE107200</accession><cross_references><GSM>GSM2862522</GSM><GSM>GSM2862523</GSM><GSM>GSM2862524</GSM><GSM>GSM2862525</GSM><GSM>GSM2862526</GSM><GSM>GSM2862527</GSM><GSM>GSM2862528</GSM><GSM>GSM2862529</GSM><GPL>4133</GPL><GSE>107200</GSE><taxon>Homo sapiens</taxon><PMID>[30180847]</PMID></cross_references></HashMap>