<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ku J</submitter><funding>Ministry of Science, ICT and Future Planning</funding><funding>This research was also supported with the computing resources by Global Science experimental Data hub Center (GSDC) &amp;amp; Korea Research Environment Open NETwork (KREONET).</funding><pagination>630</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7599330</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>3(1)</volume><pubmed_abstract>Aminoacyl-tRNA synthetase-interacting multifunctional protein 2 (AIMP2) is a non-enzymatic component required for the multi-tRNA synthetase complex. While exon 2 skipping alternatively spliced variant of AIMP2 (AIMP2-DX2) compromises AIMP2 activity and is associated with carcinogenesis, its clinical potential awaits further validation. Here, we found that AIMP2-DX2/AIMP2 expression ratio is strongly correlated with major cancer signaling pathways and poor prognosis, particularly in acute myeloid leukemia (AML). Analysis of a clinical patient cohort revealed that AIMP2-DX2 positive AML patients show decreased overall survival and progression-free survival. We also developed targeted RNA-sequencing and single-molecule RNA-FISH tools to quantitatively analyze AIMP2-DX2/AIMP2 ratios at the sin</pubmed_abstract><journal>Communications biology</journal><pubmed_title>Single-cell analysis of AIMP2 splice variants informs on drug sensitivity and prognosis in hematologic cancer.</pubmed_title><pmcid>PMC7599330</pmcid><funding_grant_id>NRF-2014M3A6A4074727</funding_grant_id><funding_grant_id>NRF-2019R1C1C1006672</funding_grant_id><pubmed_authors>Kim S</pubmed_authors><pubmed_authors>Kim D</pubmed_authors><pubmed_authors>Kim R</pubmed_authors><pubmed_authors>Lee N</pubmed_authors><pubmed_authors>Ku J</pubmed_authors><pubmed_authors>Yoon SS</pubmed_authors><pubmed_authors>Song S</pubmed_authors><pubmed_authors>Lee K</pubmed_authors><pubmed_authors>Koh Y</pubmed_authors><pubmed_authors>Kim Y</pubmed_authors><pubmed_authors>Kwon NH</pubmed_authors><pubmed_authors>Kim M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-cell analysis of AIMP2 splice variants informs on drug sensitivity and prognosis in hematologic cancer.</name><description>Aminoacyl-tRNA synthetase-interacting multifunctional protein 2 (AIMP2) is a non-enzymatic component required for the multi-tRNA synthetase complex. While exon 2 skipping alternatively spliced variant of AIMP2 (AIMP2-DX2) compromises AIMP2 activity and is associated with carcinogenesis, its clinical potential awaits further validation. Here, we found that AIMP2-DX2/AIMP2 expression ratio is strongly correlated with major cancer signaling pathways and poor prognosis, particularly in acute myeloid leukemia (AML). Analysis of a clinical patient cohort revealed that AIMP2-DX2 positive AML patients show decreased overall survival and progression-free survival. We also developed targeted RNA-sequencing and single-molecule RNA-FISH tools to quantitatively analyze AIMP2-DX2/AIMP2 ratios at the sin</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Oct</publication><modification>2025-06-01T03:53:32.805Z</modification><creation>2025-06-01T03:53:32.805Z</creation></dates><accession>S-EPMC7599330</accession><cross_references><pubmed>33128014</pubmed><doi>10.1038/s42003-020-01353-x</doi></cross_references></HashMap>