<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fan T</submitter><funding>National Natural Science Foundation of China</funding><pagination>369</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10514036</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>Histone H3 lysine 4 trimethylation (H3K4me3) is a canonical chromatin modification associated with active gene transcription, playing a pivotal role in regulating various cellular functions. Components of the H3K4me3 methyltransferase complex, known as the proteins associated with SET1 (COMPASS), have been implicated in exerting cancer-protective or cancer-inhibitory effects through inducive H3K4me3 modification. However, the role of the indispensable non-catalytic component of COMPASS CXXC-type zinc finger protein 1 (CFP1) in malignant progression remains unclear. We have unveiled that CFP1 promote lung adenocarcinoma (LUAD) cell proliferation, migration, and invasion while impairing cell apoptosis through in vitro and in vivo models. In addition, high CFP1 expression was identified as em</pubmed_abstract><journal>Signal transduction and targeted therapy</journal><pubmed_title>CXXC finger protein 1 (CFP1) bridges the reshaping of genomic H3K4me3 signature to the advancement of lung adenocarcinoma.</pubmed_title><pmcid>PMC10514036</pmcid><funding_grant_id>81972196</funding_grant_id><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Tian H</pubmed_authors><pubmed_authors>Xiao C</pubmed_authors><pubmed_authors>Fan T</pubmed_authors><pubmed_authors>Wang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>CXXC finger protein 1 (CFP1) bridges the reshaping of genomic H3K4me3 signature to the advancement of lung adenocarcinoma.</name><description>Histone H3 lysine 4 trimethylation (H3K4me3) is a canonical chromatin modification associated with active gene transcription, playing a pivotal role in regulating various cellular functions. Components of the H3K4me3 methyltransferase complex, known as the proteins associated with SET1 (COMPASS), have been implicated in exerting cancer-protective or cancer-inhibitory effects through inducive H3K4me3 modification. However, the role of the indispensable non-catalytic component of COMPASS CXXC-type zinc finger protein 1 (CFP1) in malignant progression remains unclear. We have unveiled that CFP1 promote lung adenocarcinoma (LUAD) cell proliferation, migration, and invasion while impairing cell apoptosis through in vitro and in vivo models. In addition, high CFP1 expression was identified as em</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Sep</publication><modification>2025-04-04T21:02:54.303Z</modification><creation>2025-04-04T21:02:54.303Z</creation></dates><accession>S-EPMC10514036</accession><cross_references><pubmed>37735441</pubmed><doi>10.1038/s41392-023-01612-3</doi></cross_references></HashMap>