<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(5)</volume><submitter>Thakur C</submitter><pubmed_abstract>Identifying metastatic tumor growth at an early stage has been one of the biggest challenges in the treatment of lung cancer. By genetic lineage tracing approach in a conditional model of Non-Small Cell Lung Cancer (NSCLC) in mice, we demonstrate that cystic lesions represent an early stage of metastatic invasion. We generated a mouse model for NSCLC which incorporated a heritable DsRed fluorescent tag driven by the ubiquitous CAG promoter in the alveolar type II cells of the lung. We found early cystic lesions in a secondary organ (liver) that lacked the expression of &lt;i>bona fide&lt;/i> lung makers namely Scgb1a1 and surfactant protein C Sftpc and were DsRed positive hence identifying lung as their source of origin. This demonstrates the significant potential of alveolar type II cells in or</pubmed_abstract><journal>Oncotarget</journal><pagination>6518-6535</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5814229</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cysts mark the early stage of metastatic tumor development in non-small cell lung cancer.</pubmed_title><pmcid>PMC5814229</pmcid><pubmed_authors>Thakur C</pubmed_authors><pubmed_authors>Rudel T</pubmed_authors><pubmed_authors>Rapp UR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cysts mark the early stage of metastatic tumor development in non-small cell lung cancer.</name><description>Identifying metastatic tumor growth at an early stage has been one of the biggest challenges in the treatment of lung cancer. By genetic lineage tracing approach in a conditional model of Non-Small Cell Lung Cancer (NSCLC) in mice, we demonstrate that cystic lesions represent an early stage of metastatic invasion. We generated a mouse model for NSCLC which incorporated a heritable DsRed fluorescent tag driven by the ubiquitous CAG promoter in the alveolar type II cells of the lung. We found early cystic lesions in a secondary organ (liver) that lacked the expression of &lt;i>bona fide&lt;/i> lung makers namely Scgb1a1 and surfactant protein C Sftpc and were DsRed positive hence identifying lung as their source of origin. This demonstrates the significant potential of alveolar type II cells in or</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jan</publication><modification>2025-04-21T14:32:20.726Z</modification><creation>2019-03-26T23:03:58Z</creation></dates><accession>S-EPMC5814229</accession><cross_references><pubmed>29464089</pubmed><doi>10.18632/oncotarget.23785</doi></cross_references></HashMap>