<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang L</submitter><funding>National Natural Science Foundation of China for Young Scholars</funding><pagination>111</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11334498</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(1)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Colorectal cancer (CRC) is a form of malignancy that exhibits a comparatively elevated occurrence and fatality rate. Given the relatively slower progress in diagnostic and therapeutic approaches for CRC, there is a need to investigate more accurate and efficient biomarkers.&lt;h4>Methods&lt;/h4>Core regulatory genes were screened using the TCGA database, and the expression of neurexophilin 4 (NXPH4) and its prognostic implications were validated using tissue microarray staining. The assessment of NXPH4 functions involved a range of experiments, including cellular, organoid, and murine models. Furthermore, a regulatory network between m&lt;sup>5&lt;/sup>C, NXPH4, and HIF1A was established through several in vitro experiments.&lt;h4>Results&lt;/h4>The overexpression of NXPH4 is associated wi</pubmed_abstract><journal>Cellular &amp; molecular biology letters</journal><pubmed_title>NXPH4 mediated by m&lt;sup>5&lt;/sup>C contributes to the malignant characteristics of colorectal cancer via inhibiting HIF1A degradation.</pubmed_title><pmcid>PMC11334498</pmcid><funding_grant_id>82303877</funding_grant_id><pubmed_authors>Xu L</pubmed_authors><pubmed_authors>Lian Z</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>He G</pubmed_authors><pubmed_authors>Xu H</pubmed_authors><pubmed_authors>Wu H</pubmed_authors><pubmed_authors>Miao K</pubmed_authors><pubmed_authors>Yin H</pubmed_authors><pubmed_authors>Sun P</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Shi J</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Zhong M</pubmed_authors></additional><is_claimable>false</is_claimable><name>NXPH4 mediated by m&lt;sup>5&lt;/sup>C contributes to the malignant characteristics of colorectal cancer via inhibiting HIF1A degradation.</name><description>&lt;h4>Objective&lt;/h4>Colorectal cancer (CRC) is a form of malignancy that exhibits a comparatively elevated occurrence and fatality rate. Given the relatively slower progress in diagnostic and therapeutic approaches for CRC, there is a need to investigate more accurate and efficient biomarkers.&lt;h4>Methods&lt;/h4>Core regulatory genes were screened using the TCGA database, and the expression of neurexophilin 4 (NXPH4) and its prognostic implications were validated using tissue microarray staining. The assessment of NXPH4 functions involved a range of experiments, including cellular, organoid, and murine models. Furthermore, a regulatory network between m&lt;sup>5&lt;/sup>C, NXPH4, and HIF1A was established through several in vitro experiments.&lt;h4>Results&lt;/h4>The overexpression of NXPH4 is associated wi</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-06-03T01:00:17.105Z</modification><creation>2024-10-18T19:42:10.299Z</creation></dates><accession>S-EPMC11334498</accession><cross_references><pubmed>39164641</pubmed><doi>10.1186/s11658-024-00630-5</doi></cross_references></HashMap>