<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu Z</submitter><funding>China National Funds for Distinguished Young Scientists</funding><funding>Shanghai Science and Technology Committee Program</funding><funding>National Natural Science Foundation of China</funding><pagination>j.issn.2095-3941.2020.0343</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8763008</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(1)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>The dysregulation of ribosome biogenesis is associated with the progression of numerous tumors, including hepatocellular carcinoma (HCC). Small nucleolar RNAs (snoRNAs) regulate ribosome biogenesis by guiding the modification of ribosomal RNAs (rRNAs). However, the underlying mechanism of this process in HCC remains elusive.&lt;h4>Methods&lt;/h4>RNA immunoprecipitation and sequencing were used to analyze RNAs targeted by ribosome proteins. The biological functions of SNORA23 were examined in HCC cells and a xenograft mouse model. To elucidate the underlying mechanisms, the 2'-O-ribose methylation level of rRNAs was evaluated by qPCR, and the key proteins in the PI3K/Akt/mTOR pathway were detected using Western blot.&lt;h4>Results&lt;/h4>Twelve snoRNAs were found to co-exist in 4 canc</pubmed_abstract><journal>Cancer biology &amp; medicine</journal><pubmed_title>SNORA23 inhibits HCC tumorigenesis by impairing the 2'-O-ribose methylation level of 28S rRNA.</pubmed_title><pmcid>PMC8763008</pmcid><funding_grant_id>81425019</funding_grant_id><funding_grant_id>32001786</funding_grant_id><funding_grant_id>18XD1405300</funding_grant_id><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Qin Q</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Jing J</pubmed_authors><pubmed_authors>Wang R</pubmed_authors><pubmed_authors>Jia Y</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Pang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>SNORA23 inhibits HCC tumorigenesis by impairing the 2'-O-ribose methylation level of 28S rRNA.</name><description>&lt;h4>Objective&lt;/h4>The dysregulation of ribosome biogenesis is associated with the progression of numerous tumors, including hepatocellular carcinoma (HCC). Small nucleolar RNAs (snoRNAs) regulate ribosome biogenesis by guiding the modification of ribosomal RNAs (rRNAs). However, the underlying mechanism of this process in HCC remains elusive.&lt;h4>Methods&lt;/h4>RNA immunoprecipitation and sequencing were used to analyze RNAs targeted by ribosome proteins. The biological functions of SNORA23 were examined in HCC cells and a xenograft mouse model. To elucidate the underlying mechanisms, the 2'-O-ribose methylation level of rRNAs was evaluated by qPCR, and the key proteins in the PI3K/Akt/mTOR pathway were detected using Western blot.&lt;h4>Results&lt;/h4>Twelve snoRNAs were found to co-exist in 4 canc</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2026-05-31T09:47:10.549Z</modification><creation>2025-04-21T17:10:25.319Z</creation></dates><accession>S-EPMC8763008</accession><cross_references><pubmed>33710804</pubmed><doi>10.20892/j.issn.2095-3941.2020.0343</doi></cross_references></HashMap>