<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>61(5)</volume><submitter>Scicluna P</submitter><pubmed_abstract>Abnormalities of the insulin‑like growth factor 2 &lt;i>(IGF2)‑H19&lt;/i> locus with the overexpression of &lt;i>IGF2&lt;/i> are frequent findings in adrenocortical carcinoma (ACC). The present study assessed the expression of RNAs and microRNAs (miRNAs/miRs) from the &lt;i>IGF2‑H19&lt;/i> locus using PCR‑based methods in ACC and adrenocortical adenoma (ACA). The results were associated with proteomics data. &lt;i>IGF2&lt;/i> was overexpressed in ACC, and its expression correlated with that of &lt;i>miR‑483‑3p&lt;/i> and &lt;i>miR‑483‑5p&lt;/i> hosted by &lt;i>IGF2&lt;/i>. The downregulated expression of &lt;i>H19&lt;/i> in ACC compared to ACA correlated with &lt;i>miR‑675&lt;/i> expression hosted by &lt;i>H19&lt;/i>. Several proteins exhibited an inverse correlation in expression and were predicted as targets of &lt;i>miR‑483‑3p&lt;/i>, &lt;i>miR‑483‑5p&lt;/i> or &lt;i>miR‑675&lt;/i>. Subsets of these proteins were differentially expressed between ACC and ACA. These included several proteins involved in mitochondrial metabolism. Among the mitochondrial respiratory complexes, complex I and IV were significantly decreased in ACC compared to ACA. The protein expression of NADH:ubiquinone oxidoreductase subunit C1 (NDUFC1), a subunit of mitochondrial respiratory complex I, was further validated as being lower in ACC compared to ACA and normal adrenals. The silencing of &lt;i>miR‑483‑5p&lt;/i> increased NDUFC1 protein expression and reduced both oxygen consumption and glycolysis rates. On the whole, the findings of the present study reveal the dysregulation of the &lt;i>IGF2‑H19&lt;/i> locus and mitochondrial respiration in ACC. These findings may provide a basis for the further understanding of the pathogenesis of ACC and may have potential values for diagnostics and treatment.</pubmed_abstract><journal>International journal of oncology</journal><pagination>140</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9529429</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Altered expression of the &lt;i>IGF2‑H19&lt;/i> locus and mitochondrial respiratory complexes in adrenocortical carcinoma.</pubmed_title><pmcid>PMC9529429</pmcid><pubmed_authors>Caramuta S</pubmed_authors><pubmed_authors>Xu C</pubmed_authors><pubmed_authors>Gao J</pubmed_authors><pubmed_authors>Lui WO</pubmed_authors><pubmed_authors>Kjellman M</pubmed_authors><pubmed_authors>Scicluna P</pubmed_authors><pubmed_authors>Hoog A</pubmed_authors><pubmed_authors>Larsson C</pubmed_authors><pubmed_authors>Frobom R</pubmed_authors><pubmed_authors>Branstrom R</pubmed_authors><pubmed_authors>Akhtar M</pubmed_authors><pubmed_authors>Ekstrom TJ</pubmed_authors><pubmed_authors>Almgren M</pubmed_authors><pubmed_authors>Kjellin H</pubmed_authors><pubmed_authors>Shi H</pubmed_authors><pubmed_authors>Zedenius J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Altered expression of the &lt;i>IGF2‑H19&lt;/i> locus and mitochondrial respiratory complexes in adrenocortical carcinoma.</name><description>Abnormalities of the insulin‑like growth factor 2 &lt;i>(IGF2)‑H19&lt;/i> locus with the overexpression of &lt;i>IGF2&lt;/i> are frequent findings in adrenocortical carcinoma (ACC). The present study assessed the expression of RNAs and microRNAs (miRNAs/miRs) from the &lt;i>IGF2‑H19&lt;/i> locus using PCR‑based methods in ACC and adrenocortical adenoma (ACA). The results were associated with proteomics data. &lt;i>IGF2&lt;/i> was overexpressed in ACC, and its expression correlated with that of &lt;i>miR‑483‑3p&lt;/i> and &lt;i>miR‑483‑5p&lt;/i> hosted by &lt;i>IGF2&lt;/i>. The downregulated expression of &lt;i>H19&lt;/i> in ACC compared to ACA correlated with &lt;i>miR‑675&lt;/i> expression hosted by &lt;i>H19&lt;/i>. Several proteins exhibited an inverse correlation in expression and were predicted as targets of &lt;i>miR‑483‑3p&lt;/i>, &lt;i>miR‑483‑5p&lt;/i> or &lt;i>miR‑675&lt;/i>. Subsets of these proteins were differentially expressed between ACC and ACA. These included several proteins involved in mitochondrial metabolism. Among the mitochondrial respiratory complexes, complex I and IV were significantly decreased in ACC compared to ACA. The protein expression of NADH:ubiquinone oxidoreductase subunit C1 (NDUFC1), a subunit of mitochondrial respiratory complex I, was further validated as being lower in ACC compared to ACA and normal adrenals. The silencing of &lt;i>miR‑483‑5p&lt;/i> increased NDUFC1 protein expression and reduced both oxygen consumption and glycolysis rates. On the whole, the findings of the present study reveal the dysregulation of the &lt;i>IGF2‑H19&lt;/i> locus and mitochondrial respiration in ACC. These findings may provide a basis for the further understanding of the pathogenesis of ACC and may have potential values for diagnostics and treatment.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-26T15:36:30.297Z</modification><creation>2025-04-06T14:57:07.233Z</creation></dates><accession>S-EPMC9529429</accession><cross_references><pubmed>36169175</pubmed><doi>10.3892/ijo.2022.5430</doi></cross_references></HashMap>