<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(4)</volume><submitter>Su H</submitter><pubmed_abstract>NSCLC is common and is the primary cause of cancer-related deaths due to a lack of early diagnosis and its propensity for metastasis. The pathogenesis of NSCLC is still unclear. Here, we explored the molecular mechanisms underlying NSCLC development, focusing on the HOXC-AS3/YBX1/HOXC8 axis. Human NSCLC specimens and cell lines were used. qRT-PCR and western blotting were utilised to examine the levels of HOXC-AS3/YBX1/HOXC8. CCK-8, colony formation, scratch wound healing and Transwell assays were performed to evaluate cancer cell proliferation, migration and invasion. A nude mouse xenograft model was used to examine tumour growth and metastasis in vivo. RNA pull-down, chromatin immunoprecipitation, coimmunoprecipitation and dual-luciferase assays were applied to validate the interactions </pubmed_abstract><journal>Cell death &amp; disease</journal><pagination>307</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8986809</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>LncRNA HOXC-AS3 promotes non-small-cell lung cancer growth and metastasis through upregulation of YBX1.</pubmed_title><pmcid>PMC8986809</pmcid><pubmed_authors>Fan G</pubmed_authors><pubmed_authors>Qiu X</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Su H</pubmed_authors></additional><is_claimable>false</is_claimable><name>LncRNA HOXC-AS3 promotes non-small-cell lung cancer growth and metastasis through upregulation of YBX1.</name><description>NSCLC is common and is the primary cause of cancer-related deaths due to a lack of early diagnosis and its propensity for metastasis. The pathogenesis of NSCLC is still unclear. Here, we explored the molecular mechanisms underlying NSCLC development, focusing on the HOXC-AS3/YBX1/HOXC8 axis. Human NSCLC specimens and cell lines were used. qRT-PCR and western blotting were utilised to examine the levels of HOXC-AS3/YBX1/HOXC8. CCK-8, colony formation, scratch wound healing and Transwell assays were performed to evaluate cancer cell proliferation, migration and invasion. A nude mouse xenograft model was used to examine tumour growth and metastasis in vivo. RNA pull-down, chromatin immunoprecipitation, coimmunoprecipitation and dual-luciferase assays were applied to validate the interactions </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-05T00:29:01.997Z</modification><creation>2025-04-05T00:29:01.997Z</creation></dates><accession>S-EPMC8986809</accession><cross_references><pubmed>35387975</pubmed><doi>10.1038/s41419-022-04723-x</doi></cross_references></HashMap>