<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tu CF</submitter><funding>Institute of Biomedical Sciences</funding><funding>Ministry of Science and Technology, Taiwan</funding><funding>Academia Sinica, Taiwan</funding><pagination>21</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8932202</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>We recently showed that fucosyltransferase 8 (FUT8)-mediated core fucosylation of transforming growth factor-β receptor enhances its signaling and promotes breast cancer invasion and metastasis. However, the complete FUT8 target glycoproteins and their downstream signaling networks critical for breast cancer progression remain largely unknown.&lt;h4>Method&lt;/h4>We performed quantitative glycoproteomics with two highly invasive breast cancer cell lines to unravel a comprehensive list of core-fucosylated glycoproteins by comparison to parental wild-type and FUT8-knockout counterpart cells. In addition, ingenuity pathway analysis (IPA) was performed to highlight the most enriched biological functions and signaling pathways mediated by FUT8 targets. Novel FUT8 target glycoprotei</pubmed_abstract><journal>Breast cancer research : BCR</journal><pubmed_title>Quantitative glycoproteomics analysis identifies novel FUT8 targets and signaling networks critical for breast cancer cell invasiveness.</pubmed_title><pmcid>PMC8932202</pmcid><funding_grant_id>MOST 110-2320-B-001-019-MY3</funding_grant_id><funding_grant_id>IBMS-CRC110-P04</funding_grant_id><funding_grant_id>AS-KPQ-111-KNT</funding_grant_id><funding_grant_id>MOST 107-2320-B-001-015-MY3</funding_grant_id><funding_grant_id>MOST 109-2320-B-001-012-MY3</funding_grant_id><funding_grant_id>AS-GC-111-L04</funding_grant_id><pubmed_authors>Li LH</pubmed_authors><pubmed_authors>Li FA</pubmed_authors><pubmed_authors>Yang RB</pubmed_authors><pubmed_authors>Tu CF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Quantitative glycoproteomics analysis identifies novel FUT8 targets and signaling networks critical for breast cancer cell invasiveness.</name><description>&lt;h4>Background&lt;/h4>We recently showed that fucosyltransferase 8 (FUT8)-mediated core fucosylation of transforming growth factor-β receptor enhances its signaling and promotes breast cancer invasion and metastasis. However, the complete FUT8 target glycoproteins and their downstream signaling networks critical for breast cancer progression remain largely unknown.&lt;h4>Method&lt;/h4>We performed quantitative glycoproteomics with two highly invasive breast cancer cell lines to unravel a comprehensive list of core-fucosylated glycoproteins by comparison to parental wild-type and FUT8-knockout counterpart cells. In addition, ingenuity pathway analysis (IPA) was performed to highlight the most enriched biological functions and signaling pathways mediated by FUT8 targets. Novel FUT8 target glycoprotei</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-26T18:31:30.425Z</modification><creation>2025-04-06T15:49:28.44Z</creation></dates><accession>S-EPMC8932202</accession><cross_references><pubmed>35303925</pubmed><doi>10.1186/s13058-022-01513-3</doi></cross_references></HashMap>