<HashMap><database>JPOST Repository</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Xlsx>https://storage.jpostdb.org/JPST003855/files/Analyzed%20data.xlsx</Xlsx><Other>https://storage.jpostdb.org/JPST003855/files/siOGT_OXA-2_GC3_1_7867.d.zip</Other><Other>https://storage.jpostdb.org/JPST003855/files/siOGT-2_GB8_1_7863.d.zip</Other><Other>https://storage.jpostdb.org/JPST003855/files/SC-1_GB1_1_7854.d.zip</Other><Other>https://storage.jpostdb.org/JPST003855/files/siOGT-3_GC1_1_7864.d.zip</Other><Other>https://storage.jpostdb.org/JPST003855/files/SC_OXA-2_GB5_1_7859.d.zip</Other><Other>https://storage.jpostdb.org/JPST003855/files/siOGT_OXA-3_GC4_1_7868.d.zip</Other><Other>https://storage.jpostdb.org/JPST003855/files/SC_OXA-3_GB6_1_7860.d.zip</Other><Other>https://storage.jpostdb.org/JPST003855/files/SC-2_GB2_1_7855.d.zip</Other><Other>https://storage.jpostdb.org/JPST003855/files/SC_OXA-1_GB4_1_7858.d.zip</Other><Other>https://storage.jpostdb.org/JPST003855/files/SC-3_GB3_1_7856.d.zip</Other><Other>https://storage.jpostdb.org/JPST003855/files/siOGT_OXA-1_GC2_1_7866.d.zip</Other><Other>https://storage.jpostdb.org/JPST003855/files/siOGT-1_GB7_1_7862.d.zip</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Proteomics</omics_type><submitter>Voraratt Champattanachai</submitter><species>Homo Sapiens (human)</species><full_dataset_link>https://repository.jpostdb.org/entry/JPST003855</full_dataset_link><submitter_affiliation>Chulabhorn Research Institute</submitter_affiliation><sample_protocol></sample_protocol><repository>jPOST</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Reducing OGT and O-GlcNAcylation enhance the anticancer effects of oxaliplatin in SW620 metastatic colorectal cancer cells</name><description>The proteins and biological processes affected by OGT knockdown and oxaliplatin in CRC SW620 cells were identified and quantified by mass spectrometry-based proteomics (LC-TIMS-MS/MS and PEAKS Studio). We found that proteins involved in several pathways such as ribosomal biosynthesis and cell cycle process were altered by these treatments.</description><dates><publication>Tue Feb 10 00:00:00 GMT 2026</publication></dates><accession>PXD064741</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>