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PXD018673

PXD018673 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleN-glycomic profiling of colorectal cancer according to tumor stage and location
DescriptionAlterations in glycosylation are seen in many types of cancer, including colorectal cancer (CRC). CRC is known to display glycosylation alterations. Glycans, the sugar moieties of glycoconjugates, are involved in many important functions relevant to cancer, such as cell signaling and adhesion, and may can be of value as biomarkers. In this study, we have used mass spectrometry to analyze the N-glycan profiles of 35 CRC tissue samples from patients with tumors in the right or left colon and 10 healthy tissue samples from non-CRC patients who underwent operations for other reasons. The tumor samples were divided into groups depending on tumor location (right or left colon) and stage (II or III), while the healthy samples were divided into right or left side of the colon. The levels of neutral and acidic N-glycan compositions and glycan classes were analyzed in a total of ten different groups. Surprisingly, there were no significant differences in glycan levels when all right- and left-sided CRC samples were compared, and few differences (such as in the abundance of the neutral N-glycan H3N5) were seen when the samples were divided according to both location and stage. Multiple significant differences were found in the levels of glycans and glycan classes when stage II and III samples were compared, and these glycans could be of value as candidates for new markers of cancer progression. In order to validate our findings, we analyzed healthy tissue samples from the right and left colon and found no significant differences in the levels of any of the glycans analyzed, confirming that our findings when comparing CRC samples from the right and left colon are not due to normal variations in the levels of glycans between the healthy right and left colon. Additionally, the levels of the acidic glycans H4N3F1P1, H5N4F1P1, and S1H5N4F1 were found to change in a cancer-specific but colon location-nonspecific manner, indicating that CRC affects glycan levels in similar ways, regardless of tumor location.
HostingRepositoryPRIDE
AnnounceDate2020-06-10
AnnouncementXMLSubmission_2020-07-05_22:22:33.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterTero Satomaa
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListmonosodium salt
Instrumentultraflex
Dataset History
RevisionDatetimeStatusChangeLog Entry
02020-04-20 06:25:17ID requested
12020-06-09 23:22:57announced
22020-07-05 22:22:34announced2020-07-06: Updated publication reference for PubMed record(s): 32598367.
Publication List
Holm M, Nummela P, Heiskanen A, Satomaa T, Kaprio T, Mustonen H, Ristim, รค, ki A, Haglund C, N-glycomic profiling of colorectal cancer according to tumor stage and location. PLoS One, 15(6):e0234989(2020) [pubmed]
Keyword List
submitter keyword: N-glycan cancer MALDI-TOF mass spectrometry
Contact List
Tero Satomaa
contact affiliationGlykos Finland Ltd., Helsinki, Finland
contact emailtero.satomaa@glykos.fi
lab head
Tero Satomaa
contact affiliationGlykos Finland Ltd.
contact emailtero.satomaa@glykos.fi
dataset submitter
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Dataset FTP location
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PRIDE project URI
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