<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu X</submitter><funding>China Postdoctoral Science Foundation</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>802</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11549417</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(11)</volume><pubmed_abstract>Glioblastoma is one of the most common and aggressive primary brain tumors. The aberration of metabolism is the important character of GBM cells and is tightly related to the malignancy of GBM. We mainly verified the regulatory effects of KHDRBS1, SNORD51 and ZBED6 on pentose phosphate pathway and malignant biological behavior in glioblastoma cells, such as proliferation, migration and invasion. KHDRBS1 and SNORD51 were upregulated in GBM tissues and cells. But ZBED6 had opposite tendency in GBM tissues and cells. KHDRBS1 may improve the stability of SNORD51 by binding to SNORD51, thus elevating the expression of SNORD51. More importantly, SNORD51 can competitively bind to WDR33 with 3'UTR of ZBED6 pre-mRNA which can inhibit the 3' end processing of ZBED6 pre-mRNA, thereby inhibiting the e</pubmed_abstract><journal>Cell death &amp; disease</journal><pubmed_title>KHDRBS1 regulates the pentose phosphate pathway and malignancy of GBM through SNORD51-mediated polyadenylation of ZBED6 pre-mRNA.</pubmed_title><pmcid>PMC11549417</pmcid><funding_grant_id>82173071</funding_grant_id><funding_grant_id>82272846</funding_grant_id><funding_grant_id>2022M723519</funding_grant_id><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Dong W</pubmed_authors><pubmed_authors>Wang P</pubmed_authors><pubmed_authors>Ruan X</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>E T</pubmed_authors><pubmed_authors>Lin H</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Xue Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>KHDRBS1 regulates the pentose phosphate pathway and malignancy of GBM through SNORD51-mediated polyadenylation of ZBED6 pre-mRNA.</name><description>Glioblastoma is one of the most common and aggressive primary brain tumors. The aberration of metabolism is the important character of GBM cells and is tightly related to the malignancy of GBM. We mainly verified the regulatory effects of KHDRBS1, SNORD51 and ZBED6 on pentose phosphate pathway and malignant biological behavior in glioblastoma cells, such as proliferation, migration and invasion. KHDRBS1 and SNORD51 were upregulated in GBM tissues and cells. But ZBED6 had opposite tendency in GBM tissues and cells. KHDRBS1 may improve the stability of SNORD51 by binding to SNORD51, thus elevating the expression of SNORD51. More importantly, SNORD51 can competitively bind to WDR33 with 3'UTR of ZBED6 pre-mRNA which can inhibit the 3' end processing of ZBED6 pre-mRNA, thereby inhibiting the e</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-07-16T21:46:03.907Z</modification><creation>2025-04-04T18:56:07.788Z</creation></dates><accession>S-EPMC11549417</accession><cross_references><pubmed>39516455</pubmed><doi>10.1038/s41419-024-07163-x</doi></cross_references></HashMap>