<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Qi TF</submitter><funding>National Institute of Environmental Health Sciences</funding><funding>NIEHS NIH HHS</funding><pagination>1525-1530</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8792366</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>94(3)</volume><pubmed_abstract>Epitranscriptomic reader, writer, and eraser (RWE) proteins recognize, install, and remove modified nucleosides in RNA, which are known to play crucial roles in RNA processing, splicing, and stability. Here, we established a liquid chromatography-parallel-reaction monitoring (LC-PRM) method for high-throughput profiling of a total of 152 epitranscriptomic RWE proteins. We also applied the LC-PRM method, in conjunction with stable isotope labeling by amino acids in cell culture (SILAC), to quantify these proteins in two pairs of matched parental/radioresistant breast cancer cells (i.e., MDA-MB-231 and MCF-7 cells and their corresponding radioresistant C5 and C6 clones), with the goal of assessing the roles of these proteins in radioresistance. We found that eight epitranscriptomic RWE prote</pubmed_abstract><journal>Analytical chemistry</journal><pubmed_title>Targeted Profiling of Epitranscriptomic Reader, Writer, and Eraser Proteins Accompanied with Radioresistance in Breast Cancer Cells.</pubmed_title><pmcid>PMC8792366</pmcid><funding_grant_id>R35 ES031707</funding_grant_id><pubmed_authors>Miao W</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Qi TF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeted Profiling of Epitranscriptomic Reader, Writer, and Eraser Proteins Accompanied with Radioresistance in Breast Cancer Cells.</name><description>Epitranscriptomic reader, writer, and eraser (RWE) proteins recognize, install, and remove modified nucleosides in RNA, which are known to play crucial roles in RNA processing, splicing, and stability. Here, we established a liquid chromatography-parallel-reaction monitoring (LC-PRM) method for high-throughput profiling of a total of 152 epitranscriptomic RWE proteins. We also applied the LC-PRM method, in conjunction with stable isotope labeling by amino acids in cell culture (SILAC), to quantify these proteins in two pairs of matched parental/radioresistant breast cancer cells (i.e., MDA-MB-231 and MCF-7 cells and their corresponding radioresistant C5 and C6 clones), with the goal of assessing the roles of these proteins in radioresistance. We found that eight epitranscriptomic RWE prote</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2026-05-27T10:51:48.809Z</modification><creation>2025-04-04T11:25:49.54Z</creation></dates><accession>S-EPMC8792366</accession><cross_references><pubmed>35021009</pubmed><doi>10.1021/acs.analchem.1c05441</doi></cross_references></HashMap>