<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8</volume><submitter>Yin Z</submitter><pubmed_abstract>Acute myeloid leukemia (AML) represents a frequently occurring adulthood acute leukemia (AL). Great progresses have been achieved in the treatment of AML, but its pathogenic mechanism remains unclear. This study reported the biological functions of lncRNA &lt;i>DUBR&lt;/i> in AML pathogenic mechanism. As a result, lncRNA &lt;i>DUBR&lt;/i> showed high expression level within AML, resulting in poor prognosis, especially in M4 AML. &lt;i>In vitro&lt;/i> studies elucidated that knockdown of &lt;i>DUBR&lt;/i> with small interfering RNA (siRNA) resulted in the suppression of survival and colony formation ability, as well as induction of apoptosis, in AML cells. RNA pull-down assay and computational revealed that &lt;i>DUBR&lt;/i> could sponge with miRNA-142-3P and interact with FUS protein. MiRNA-142-3P have a negative corre</pubmed_abstract><journal>Frontiers in molecular biosciences</journal><pagination>754936</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8570042</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>MiRNA-142-3P and FUS can be Sponged by Long Noncoding RNA &lt;i>DUBR&lt;/i> to Promote Cell Proliferation in Acute Myeloid Leukemia.</pubmed_title><pmcid>PMC8570042</pmcid><pubmed_authors>Gu CM</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Shen H</pubmed_authors><pubmed_authors>Zhang MQ</pubmed_authors><pubmed_authors>Wu F</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors><pubmed_authors>Yin Z</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Zhong Q</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Ou R</pubmed_authors></additional><is_claimable>false</is_claimable><name>MiRNA-142-3P and FUS can be Sponged by Long Noncoding RNA &lt;i>DUBR&lt;/i> to Promote Cell Proliferation in Acute Myeloid Leukemia.</name><description>Acute myeloid leukemia (AML) represents a frequently occurring adulthood acute leukemia (AL). Great progresses have been achieved in the treatment of AML, but its pathogenic mechanism remains unclear. This study reported the biological functions of lncRNA &lt;i>DUBR&lt;/i> in AML pathogenic mechanism. As a result, lncRNA &lt;i>DUBR&lt;/i> showed high expression level within AML, resulting in poor prognosis, especially in M4 AML. &lt;i>In vitro&lt;/i> studies elucidated that knockdown of &lt;i>DUBR&lt;/i> with small interfering RNA (siRNA) resulted in the suppression of survival and colony formation ability, as well as induction of apoptosis, in AML cells. RNA pull-down assay and computational revealed that &lt;i>DUBR&lt;/i> could sponge with miRNA-142-3P and interact with FUS protein. MiRNA-142-3P have a negative corre</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2025-04-04T08:33:21.782Z</modification><creation>2022-02-11T12:37:42.374Z</creation></dates><accession>S-EPMC8570042</accession><cross_references><pubmed>34746238</pubmed><doi>10.3389/fmolb.2021.754936</doi></cross_references></HashMap>