PXD037033 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | What do the transcriptome and proteome of menstrual blood derived mesenchymal stem cells tell us about endometriosis? |
Description | Given the importance of menstrual blood in the pathogenesis of endometriosis and the multifunctional roles of menstrual mesenchymal stem cells (MenSCs) in regenerative medicine, this issue has gained prominence in the scientific community. Moreover, recent reviews highlight how robust the integrated assessment of omics data is for endometriosis. To our knowledge, no study has applied the multi-omics approaches to endometriosis MenSCs. It is a case-control study at a university-affiliated hospital. MenSCs transcriptome and proteome data were obtained by RNA-seq and UHPLC- MS/MS detection. Among the differentially expressed proteins and genes, we emphasize ATF3, ID1, ID3, FOSB, SNAI1, NR4A1, EGR1, LAMC3, and ZFP36 genes and MT2A, TYMP, COL1A1, COL6A2, and NID2 proteins that were already reported in the endometriosis. Our functional enrichment analysis reveals integrated modulating signaling pathways such as epithelial-mesenchymal transition (↑) and PI3K signaling via AKT to mTORC1 (↓in proteome), mTORC1 signaling, TGF beta signaling, TNFA signaling via NFkB, and response to hypoxia via HIF1A targets (↑in transcriptome). Our findings highlight primary changes in the endometriosis MenSCs, suggesting that the chronic inflammatory endometrial microenvironment can modulate these cells, providing opportunities for endometriosis etiopathogenesis. Moreover, they identify challenges for future research leveraging knowledge for regenerative and precision medicine in endometriosis. |
HostingRepository | PRIDE |
AnnounceDate | 2023-11-14 |
AnnouncementXML | Submission_2023-11-14_08:36:11.288.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Vitor Faca |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | iodoacetamide derivatized residue |
Instrument | Q Exactive HF |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2022-09-27 11:27:19 | ID requested | |
1 | 2023-03-10 19:53:15 | announced | |
⏵ 2 | 2023-11-14 08:36:13 | announced | 2023-11-14: Updated project metadata. |
Publication List
Penariol LBC, Thom, é CH, Tozetti PA, Paier CRK, Buono FO, Peronni KC, Orellana MD, Covas DT, Moraes MEA, Silva WA, Rosa-E-Silva JC, Ferriani RA, Fa, ç, a VM, Poli-Neto OB, Tiezzi DG, Meola J, What Do the Transcriptome and Proteome of Menstrual Blood-Derived Mesenchymal Stem Cells Tell Us about Endometriosis? Int J Mol Sci, 23(19):(2022) [pubmed] |
Keyword List
submitter keyword: Endometriosis, mesenchymal cells |
Contact List
Juliana Meola |
contact affiliation | Department of Gynecology and Obstetrics - Ribeirao Preto Medical School - University of Sao Paulo |
contact email | jumeola@usp.br |
lab head | |
Vitor Faca |
contact affiliation | University of Sao Paulo |
contact email | vitor.faca@fmrp.usp.br |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD037033
- Label: PRIDE project
- Name: What do the transcriptome and proteome of menstrual blood derived mesenchymal stem cells tell us about endometriosis?