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PXD057700

PXD057700 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleUncovering biological heterogeneity in endometrial carcinoma molecular subtypes by proteomic analysis
DescriptionWhile endometrial cancer (EC) has an overall favorable prognosis, some patients do poorly and may benefit from refinements of current classification systems. Molecular classification stratifies ECs into four prognostic groups: POLEmut, MMRd (mismatch repair deficient), p53abn, and NSMP (no specific molecular profile), where POLEmut has the best prognosis and p53abn has the worst prognosis. We used proteomic profiling to provide additional prognostic or predictive information for EC patients, across or within molecular subtypes. Global proteome profiling of formalin fixed, paraffin embedded samples, that had clinicopathologic and outcome data, was performed on 184 ECs encompassing all four molecular subtypes, including replicate samples of the same tumor, and both biopsy and final hysterectomy specimens. To ensure representation of each subtype, we profiled an approximately equal distribution in the 148 unique tumors; 34 (23%) POLEmut, 40 (23%) MMRd, 35 (24%) p53abn and 39 (26%) NSMP, rather than the population-based distributions. There was high reproducibility in the proteomic profiles of intra-tumor replicate samples, and between matched biopsy and hysterectomy tumor samples. Consensus clustering identified four clusters with different prognosis, named ‘Adhesion’, ‘Immune’, ‘Proliferation’, and ‘Metabolic’ based on proteins enriched in each cluster. We correlated protein expression with common mutations, molecular subtypes, and outcomes. Proteomic analysis of EC identified candidate prognostic markers that may further refine current molecular classification and help guide treatment decisions. These data offer insights into new therapeutic interventions that could be developed to target proteins and pathways identified by EC proteomic profiling.
HostingRepositoryPRIDE
AnnounceDate2025-10-07
AnnouncementXMLSubmission_2025-10-06_16:30:05.950.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterGian Luca Negri
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606;
ModificationListTMT6plex-126 reporter+balance reagent acylated residue
InstrumentOrbitrap Fusion
Dataset History
RevisionDatetimeStatusChangeLog Entry
02024-11-09 13:11:47ID requested
12025-10-06 16:30:06announced
Publication List
10.1016/j.neo.2025.101229;
Cochrane DR, Negri GL, Huvila J, Kalantari F, Farnell DA, Mohammad N, Thompson E, Yang W, Lum A, Spencer SE, Riley R, Jamieson A, Leung S, Chiu D, Chow C, Lim JLP, K, ö, bel M, Kommoss S, Kommoss F, Gilks B, Hoang L, Huntsman DG, Morin GB, McAlpine JN, Proteomic analysis uncovers biological diversity in molecularly defined endometrial carcinomas. Neoplasia, 69():101229(2025) [pubmed]
Keyword List
submitter keyword: ffpe,endometrial carcinoma, tmt
Contact List
Gregg Morin
contact affiliationCanada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver V5Z 1L3, Canada.
contact emailgmorin@bcgsc.ca
lab head
Gian Luca Negri
contact affiliationCanada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver V5Z 1L3, Canada.
contact emailgnegri@bcgsc.ca
dataset submitter
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Dataset FTP location
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