<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2022</volume><submitter>Sun Q</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>The purpose of this study was to explore the role of the lncRNA MNX1-AS1 and its related downstream signaling pathways in colorectal adenocarcinoma (COAD).&lt;h4>Methods&lt;/h4>COAD tissues and cells were prepared and treated with sh-MNX1-AS1, pcDNA-MNX1-AS1, sh-PPFIA4, LY29004, and their controls. CCK8 and colony formation assays were undertaken for evaluating cell proliferation. Tumor cell migratory ability was detected by transwell assay. Apoptosis detection was processed by YO-PRO-1/PI Staining. The regulated relationship between lncRNA MNX1-AS1 and PPFIA4 was confirmed by RIP-ChIP assay. Q-PCR was applied to detect genes related to tumor cell stemness, proliferation, migration, and apoptosis in each group. Finally, a xenograft tumor model was constructed to verify the result</pubmed_abstract><journal>Journal of oncology</journal><pagination>8303409</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9550508</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Overexpression of LncRNA MNX1-AS1/PPFIA4 Activates AKT/HIF-1&lt;i>α&lt;/i> Signal Pathway to Promote Stemness of Colorectal Adenocarcinoma Cells.</pubmed_title><pmcid>PMC9550508</pmcid><pubmed_authors>Zhu J</pubmed_authors><pubmed_authors>Sun Q</pubmed_authors><pubmed_authors>Hu H</pubmed_authors><pubmed_authors>Zhao W</pubmed_authors><pubmed_authors>Gui Z</pubmed_authors><pubmed_authors>Zhao Z</pubmed_authors><pubmed_authors>Xu W</pubmed_authors><pubmed_authors>Gao C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Overexpression of LncRNA MNX1-AS1/PPFIA4 Activates AKT/HIF-1&lt;i>α&lt;/i> Signal Pathway to Promote Stemness of Colorectal Adenocarcinoma Cells.</name><description>&lt;h4>Purpose&lt;/h4>The purpose of this study was to explore the role of the lncRNA MNX1-AS1 and its related downstream signaling pathways in colorectal adenocarcinoma (COAD).&lt;h4>Methods&lt;/h4>COAD tissues and cells were prepared and treated with sh-MNX1-AS1, pcDNA-MNX1-AS1, sh-PPFIA4, LY29004, and their controls. CCK8 and colony formation assays were undertaken for evaluating cell proliferation. Tumor cell migratory ability was detected by transwell assay. Apoptosis detection was processed by YO-PRO-1/PI Staining. The regulated relationship between lncRNA MNX1-AS1 and PPFIA4 was confirmed by RIP-ChIP assay. Q-PCR was applied to detect genes related to tumor cell stemness, proliferation, migration, and apoptosis in each group. Finally, a xenograft tumor model was constructed to verify the result</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-21T16:53:17.931Z</modification><creation>2025-04-21T16:53:17.931Z</creation></dates><accession>S-EPMC9550508</accession><cross_references><pubmed>36226248</pubmed><doi>10.1155/2022/8303409</doi></cross_references></HashMap>