PXD019425 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Altered N-linked Glycosylation in Endometrial Cancer |
Description | It has been recognised for a long time that cell surface glycans plays a vital role in the biological process and their altered form can lead to cancer. However, the molecular details and regulatory mechanism between the glycans and cancer is yet not clear. Over the past decade mass spectrometry-based techniques has become a prominent method for analysing glycans especially N-glycan matrix assisted laser desorption/ionisation mass spectrometry imaging (MALDI MSI). It is a powerful technique that combines mass spectrometry with histology, enabling the visualisation and label free detection of N-linked glycans on a single tissue section. Here, we carried out N-glycan MALDI MSI on six endometrial cancer (EC) formalin fixed paraffin embedded (FFPE) tissue sections including the adjacent normal endometrium, and tissue microarrays (TMA) consisting of 8 EC patients with lymph node metastasis (LNM) and 20 without LNM. By doing that several m/z values were detected that can significantly distinguish normal endometrium from cancerous. Also, detected a m/z value that can discriminate the primary tumour with LNM from those without. Identification of those discriminative m/z values was performed using porous graphitized carbon liquid chromatography tandem mass spectrometry (PGC-LC-MS/MS). Overall, we observed higher abundance of oligomannose in tumour regions compared to normal with AUC ranges from 0.85-0.99. Whereas, complex N-glycans were detected in lower abundance with AUC ranges from 0.03-0.28. Comparison of N-glycans between the primary tumours with LNM and without LNM indicates reduced abundance of a complex core-fucosylated N-glycan in patients with metastasis relative to without. In summary, N-glycan MALDI MSI can be used to characterize the cancerous endometrium from the normal, also patients with LNM from those without. Identification of those discriminative m/z values was performed using porous graphitized carbon liquid chromatography tandem mass spectrometry (PGC-LC-MS/MS). |
HostingRepository | PRIDE |
AnnounceDate | 2020-11-27 |
AnnouncementXML | Submission_2020-11-27_07:54:22.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Parul Mittal |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | No PTMs are included in the dataset |
Instrument | ultraflex |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2020-05-27 17:11:50 | ID requested | |
⏵ 1 | 2020-11-27 07:54:22 | announced | |
Publication List
Mittal P, Briggs M, Klingler-Hoffmann M, Kaur G, Packer NH, Oehler MK, Hoffmann P, Altered N-linked glycosylation in endometrial cancer. Anal Bioanal Chem, 413(10):2721-2733(2021) [pubmed] |
Keyword List
submitter keyword: Biomarker, Endometrial cancer, Lymph node metastasis, Glycan Imaging |
Contact List
Prof Peter Hoffmann |
contact affiliation | Future Industries Institute, Mawson Lakes Campus, University of South Australia, Adelaide, South Australia, 5095 |
contact email | peter.hoffmann@unisa.edu.au |
lab head | |
Parul Mittal |
contact affiliation | Research associate |
contact email | pearl106@gmail.com |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD019425
- Label: PRIDE project
- Name: Altered N-linked Glycosylation in Endometrial Cancer