<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen X</submitter><funding>National Natural Science Foundation of China</funding><pagination>2208707</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10184595</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(1)</volume><pubmed_abstract>Glutathione peroxidase 8 (GPX8) is a key regulator of redox homoeostasis. Whether its antioxidant activity participates in the regulation of m&lt;sup>6&lt;/sup>A modification is a crucial issue, which has important application value in cancer treatment. In this study, MeRIP-seq was used to explore the characteristics of transcriptome-wide m&lt;sup>6&lt;/sup>A modification in GPX8-deficient oral cancer cells. Oxidative stress caused by the lack of GPX8 resulted in 1,279 hyper- and 2,287 hypo-methylated m&lt;sup>6&lt;/sup>A peaks and 2,036 differentially expressed genes in GPX8-KO cells. Twenty-eight differentially expressed genes were related to the cell response to oxidative stress, and half of them changed their m&lt;sup>6&lt;/sup>A modification. In GPX8-KO cells, m&lt;sup>6&lt;/sup>A regulators IGF2BP2 and IGF2BP3 we</pubmed_abstract><journal>Epigenetics</journal><pubmed_title>GPX8 deficiency-induced oxidative stress reprogrammed m6A epitranscriptome of oral cancer cells.</pubmed_title><pmcid>PMC10184595</pmcid><funding_grant_id>81873711</funding_grant_id><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>He Y</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Yuan L</pubmed_authors><pubmed_authors>Zhao W</pubmed_authors><pubmed_authors>Yu D</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Chen S</pubmed_authors></additional><is_claimable>false</is_claimable><name>GPX8 deficiency-induced oxidative stress reprogrammed m6A epitranscriptome of oral cancer cells.</name><description>Glutathione peroxidase 8 (GPX8) is a key regulator of redox homoeostasis. Whether its antioxidant activity participates in the regulation of m&lt;sup>6&lt;/sup>A modification is a crucial issue, which has important application value in cancer treatment. In this study, MeRIP-seq was used to explore the characteristics of transcriptome-wide m&lt;sup>6&lt;/sup>A modification in GPX8-deficient oral cancer cells. Oxidative stress caused by the lack of GPX8 resulted in 1,279 hyper- and 2,287 hypo-methylated m&lt;sup>6&lt;/sup>A peaks and 2,036 differentially expressed genes in GPX8-KO cells. Twenty-eight differentially expressed genes were related to the cell response to oxidative stress, and half of them changed their m&lt;sup>6&lt;/sup>A modification. In GPX8-KO cells, m&lt;sup>6&lt;/sup>A regulators IGF2BP2 and IGF2BP3 we</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2025-04-25T22:33:29.563Z</modification><creation>2025-04-06T09:03:59.741Z</creation></dates><accession>S-EPMC10184595</accession><cross_references><pubmed>37170591</pubmed><doi>10.1080/15592294.2023.2208707</doi></cross_references></HashMap>