<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(24)</volume><submitter>Cao X</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Lung adenocarcinoma (LUAD) is the most common type of lung cancer, and its pathogenesis is still unclear. The present study aimed to investigate the role of &lt;i>miR-202-3p&lt;/i> and its downstream target gene, ribonucleotide reductase regulatory subunit M2 (&lt;i>RRM2&lt;/i>), in the occurrence and development of LUAD and elucidate the correlation between &lt;i>RRM2&lt;/i> and the clinicopathological stage and prognosis of LUAD.&lt;h4>Methods&lt;/h4>The expression of &lt;i>miR-202-3p&lt;/i> was analyzed using the CancerMIRNome database and quantitative polymerase chain reaction (qPCR). The effects of &lt;i>miR-202-3p&lt;/i> and &lt;i>RRM2&lt;/i> on the proliferation, migration, and invasion of A549 cells were analyzed. A dual luciferase reporter assay was used to verify the targeting of &lt;i>miR-202-3p&lt;/i> and </pubmed_abstract><journal>Annals of translational medicine</journal><pagination>1374</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9843311</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>MiR-202-3p inhibits the proliferation and metastasis of lung adenocarcinoma cells by targeting RRM2.</pubmed_title><pmcid>PMC9843311</pmcid><pubmed_authors>Xue F</pubmed_authors><pubmed_authors>Shen L</pubmed_authors><pubmed_authors>Huang F</pubmed_authors><pubmed_authors>Cao X</pubmed_authors><pubmed_authors>Zong Y</pubmed_authors><pubmed_authors>Chen H</pubmed_authors><pubmed_authors>Yuan X</pubmed_authors><pubmed_authors>Zhong L</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>MiR-202-3p inhibits the proliferation and metastasis of lung adenocarcinoma cells by targeting RRM2.</name><description>&lt;h4>Background&lt;/h4>Lung adenocarcinoma (LUAD) is the most common type of lung cancer, and its pathogenesis is still unclear. The present study aimed to investigate the role of &lt;i>miR-202-3p&lt;/i> and its downstream target gene, ribonucleotide reductase regulatory subunit M2 (&lt;i>RRM2&lt;/i>), in the occurrence and development of LUAD and elucidate the correlation between &lt;i>RRM2&lt;/i> and the clinicopathological stage and prognosis of LUAD.&lt;h4>Methods&lt;/h4>The expression of &lt;i>miR-202-3p&lt;/i> was analyzed using the CancerMIRNome database and quantitative polymerase chain reaction (qPCR). The effects of &lt;i>miR-202-3p&lt;/i> and &lt;i>RRM2&lt;/i> on the proliferation, migration, and invasion of A549 cells were analyzed. A dual luciferase reporter assay was used to verify the targeting of &lt;i>miR-202-3p&lt;/i> and </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-04T08:29:20.217Z</modification><creation>2025-04-04T08:29:20.217Z</creation></dates><accession>S-EPMC9843311</accession><cross_references><pubmed>36660663</pubmed><doi>10.21037/atm-22-6089</doi></cross_references></HashMap>