PXD021413 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Inflammatory Signaling is Regulated by Fucosylation in Metastatic Breast Cancer Cells |
Description | N-linked glycosylation results in a large branched tree-like sugar structure composed of several types of individual carbohydrates being attached to a protein. Fucosylation is one specific type of glycosylation that is defined by the addition of α-L-fucose to a carrier protein. Although fucosylation has been relatively well defined as a biomarker for progression in some human cancers, for example, pancreatic and hepatocellular carcinoma, its role in breast cancer is much less well defined. A growing body of evidence indicates that levels of fucosylation correlate with breast cancer progression and contributes to metastatic disease. However, very little is known about the signaling and functional outcomes that are driven by fucosylation. We performed tandem- mass-tag (TMT) proteomics on 4T1 metastatic mammary tumor cells that were treated with a fucosylation inhibitor, 2-fluorofucose (2FF) or vehicle (DMSO) control. This analysis identified >400 proteins that were significantly increased or decreased in 2FF treated samples compared to the DMSO treated samples. We found that two proteins, Tollip and Bcl-10, were downregulated in 4T1 cells in response to 2FF treatment. Functionally, Tollip and Bcl10 signaling induce pro-inflammatory responses through activation of NF-κB, a transcription factor that is pro-tumorigenic and a prime target in human cancer. Our results show that treatment of 4T1 cells with 2FF leads to a reduction in NF-κB expression and activity through increased IκBα. This observation is consistent with a reduction in inflammatory response due to the loss of Tollip and Bcl-10 expression. Collectively, our results indicate that fucosylation is a key mediator of inflammatory signaling in metastatic breast cancer cells. |
HostingRepository | PRIDE |
AnnounceDate | 2020-12-21 |
AnnouncementXML | Submission_2020-12-21_03:53:32.xml |
DigitalObjectIdentifier | https://dx.doi.org/10.6019/PXD021413 |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Supported dataset by repository |
PrimarySubmitter | Emma Doud |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | TMT6plex-126 reporter+balance reagent acylated residue; iodoacetamide derivatized residue |
Instrument | Orbitrap Fusion Lumos |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2020-09-10 23:07:54 | ID requested | |
⏵ 1 | 2020-12-21 03:53:32 | announced | |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: fucosylation |
N-glycsoylation |
breast cancer, metastasis, NF-κB |
Contact List
Elizabeth Yeh |
contact affiliation | Associate Professor of Pharmacology & Toxicology, Indiana University School of Medicine, Indianapolis, IN |
contact email | esyeh@iu.edu |
lab head | |
Emma Doud |
contact affiliation | Indiana University School of Medicine |
contact email | edoud@iu.edu |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD021413
- Label: PRIDE project
- Name: Inflammatory Signaling is Regulated by Fucosylation in Metastatic Breast Cancer Cells