<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rojo-Pardillo M</submitter><funding>Héger-Masson Foundation</funding><funding>David et Alice Van Buuren Foundation</funding><funding>Rose et Jean Hoguet Foundation</funding><funding>Fund for Scientific Research - FRIA grant</funding><funding>King Baudouin Foundation - Fund Doctor J.P. Naets</funding><funding>Fund for Scientific Research - Research credit</funding><funding>Jaumotte-Demoulin Foundation</funding><pagination>1465</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12468101</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(18)</volume><pubmed_abstract>Beyond well-known genetic drivers, microRNA dysregulation has emerged as a key contributor to thyroid tumorigenesis. Central to this process is &lt;i>Dicer1&lt;/i>, a ribonuclease essential for microRNA maturation, whose expression is often reduced in papillary thyroid carcinoma (PTC). Evidence from previous studies suggest &lt;i>Dicer1&lt;/i> functions as a context-dependent haplo-insufficient tumor suppressor gene: partial loss may promote tumor development, whereas complete loss may disrupt essential cellular functions, causing cell death and tumor suppression. However, the effects of partial or complete &lt;i>Dicer1&lt;/i> loss in thyroid cancer remain unclear. To explore this, we genetically inactivated one (heterozygous) or both (homozygous) &lt;i>Dicer1&lt;/i> alleles specifically in thyroid follicular cel</pubmed_abstract><journal>Cells</journal><pubmed_title>&amp;lt;i&amp;gt;Dicer1&amp;lt;/i&amp;gt; Depletion Leads to DNA Damage Accumulation and Cell Death in a RET/PTC3 Papillary Thyroid Cancer Mouse Model, Thereby Inhibiting Tumor Progression.</pubmed_title><pmcid>PMC12468101</pmcid><funding_grant_id>CDR J.0150.25</funding_grant_id><funding_grant_id>FC36079</funding_grant_id><funding_grant_id>CDR J.0123.23</funding_grant_id><funding_grant_id>2023-J1813300-233020</funding_grant_id><funding_grant_id>2025-J1813300-0025101</funding_grant_id><pubmed_authors>Kero J</pubmed_authors><pubmed_authors>Rojo-Pardillo M</pubmed_authors><pubmed_authors>Robaye B</pubmed_authors><pubmed_authors>Augenlicht A</pubmed_authors><pubmed_authors>Maenhaut C</pubmed_authors><pubmed_authors>Dom G</pubmed_authors></additional><is_claimable>false</is_claimable><name>&amp;lt;i&amp;gt;Dicer1&amp;lt;/i&amp;gt; Depletion Leads to DNA Damage Accumulation and Cell Death in a RET/PTC3 Papillary Thyroid Cancer Mouse Model, Thereby Inhibiting Tumor Progression.</name><description>Beyond well-known genetic drivers, microRNA dysregulation has emerged as a key contributor to thyroid tumorigenesis. Central to this process is &lt;i>Dicer1&lt;/i>, a ribonuclease essential for microRNA maturation, whose expression is often reduced in papillary thyroid carcinoma (PTC). Evidence from previous studies suggest &lt;i>Dicer1&lt;/i> functions as a context-dependent haplo-insufficient tumor suppressor gene: partial loss may promote tumor development, whereas complete loss may disrupt essential cellular functions, causing cell death and tumor suppression. However, the effects of partial or complete &lt;i>Dicer1&lt;/i> loss in thyroid cancer remain unclear. To explore this, we genetically inactivated one (heterozygous) or both (homozygous) &lt;i>Dicer1&lt;/i> alleles specifically in thyroid follicular cel</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-01T03:22:16.717Z</modification><creation>2026-05-01T03:11:07.435Z</creation></dates><accession>S-EPMC12468101</accession><cross_references><pubmed>41002430</pubmed><doi>10.3390/cells14181465</doi></cross_references></HashMap>