PXD041186 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | SAA1-dependent reprogramming of adipocytes by tumor cells is associated with triple negative breast cancer aggressiveness |
Description | Cancer development and progression depend on tumor cell intrinsic factors, the tumor microenvironment and host characteristics. Despite the identification of the plasticity of adipocytes, the primary breast stromal cells, both in physiology and cancer, we lack a complete understanding of mechanisms that regulate adipocyte-tumor cell crosstalk. Here we dissected the breast cancer crosstalk with adipocytes and studied relevant molecules. We identified that the ability of breast cancer cells to dedifferentiate adipocytes is intrinsic subtype-dependent, with all breast cancer subtypes, except for HER2+ER+ subtype, capable of inducing this phenomenon. Crosstalk between breast cancer cells and adipocytes in vitro increased cancer stem-like features and recruitment of pro-tumorigenic immune cells, through chemokine production. Serum amyloid A1 (SAA1) was in vitro identified as a regulator of the adipocyte dedifferentiation program in triple-negative breast cancer (TNBC) through CD36 and P2XR7 signaling. In human TNBCs, SAA1 expression was associated with CAA infiltration, inflammation, stimulated lipolysis, stem-like properties and distinct tumor immune microenvironment. Our findings provide evidence that interaction between tumor cells and adipocytes through SAA1 release is relevant to the aggressiveness of TNBC, potentially supporting its targeting. |
HostingRepository | PRIDE |
AnnounceDate | 2024-01-15 |
AnnouncementXML | Submission_2024-01-15_08:00:08.926.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Simona Nonnis |
SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
ModificationList | acetylated residue; monohydroxylated residue; deamidated residue; iodoacetamide derivatized residue |
Instrument | Q Exactive HF |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2023-03-29 06:35:39 | ID requested | |
⏵ 1 | 2024-01-15 08:00:09 | announced | |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: Proteomics |
nanoLC-MS/MS |
Contact List
Elisa Maffioli |
contact affiliation | DIVAS University of Milan, Italy |
contact email | elisa.maffioli@unimi.it |
lab head | |
Simona Nonnis |
contact affiliation | University of Milan |
contact email | simona.nonnis@unimi.it |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2024/01/PXD041186 |
PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD041186
- Label: PRIDE project
- Name: SAA1-dependent reprogramming of adipocytes by tumor cells is associated with triple negative breast cancer aggressiveness