<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24(1)</volume><submitter>Wang R</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Bladder cancer (BC) is one of the most common malignancies of the genitourinary system. Phosphofructokinase 1 (PFK-1) is one of member of PFK, which plays an important role in reprogramming cancer metabolism, such as lactylation modification. Zinc finger E-box-binding homeobox 1 (ZEB1) has been demonstrated to be a oncogene in many cancers. Therefore, this study was performed to explore the effects of PFK-1 on the lactylation of ZEB1 in BC development.&lt;h4>Methods&lt;/h4>Cell viability was measured using the CCK-8 kit. The glucose assay kit and lactate assay kit were used to detect glucose utilization and lactate production. The DNA was purified and quantified by qRT-PCR.&lt;h4>Results&lt;/h4>In the present study, we found that ZEB1 expression levels were significantly elevated in</pubmed_abstract><journal>BMC urology</journal><pagination>59</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10935987</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The mechanism of PFK-1 in the occurrence and development of bladder cancer by regulating ZEB1 lactylation.</pubmed_title><pmcid>PMC10935987</pmcid><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Wang R</pubmed_authors><pubmed_authors>Cao J</pubmed_authors><pubmed_authors>Xu F</pubmed_authors><pubmed_authors>Hu L</pubmed_authors><pubmed_authors>She Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>The mechanism of PFK-1 in the occurrence and development of bladder cancer by regulating ZEB1 lactylation.</name><description>&lt;h4>Background&lt;/h4>Bladder cancer (BC) is one of the most common malignancies of the genitourinary system. Phosphofructokinase 1 (PFK-1) is one of member of PFK, which plays an important role in reprogramming cancer metabolism, such as lactylation modification. Zinc finger E-box-binding homeobox 1 (ZEB1) has been demonstrated to be a oncogene in many cancers. Therefore, this study was performed to explore the effects of PFK-1 on the lactylation of ZEB1 in BC development.&lt;h4>Methods&lt;/h4>Cell viability was measured using the CCK-8 kit. The glucose assay kit and lactate assay kit were used to detect glucose utilization and lactate production. The DNA was purified and quantified by qRT-PCR.&lt;h4>Results&lt;/h4>In the present study, we found that ZEB1 expression levels were significantly elevated in</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-07-14T21:22:16.197Z</modification><creation>2026-06-24T03:12:51.19Z</creation></dates><accession>S-EPMC10935987</accession><cross_references><pubmed>38481182</pubmed><doi>10.1186/s12894-024-01444-5</doi></cross_references></HashMap>