Novel Diagnostic Biomarker BST2 Identified by Integrated Transcriptomics Promotes the Development of Endometriosis via the TNF-α/NF-κB Signaling Pathway

article OA: closed CC0 ⤵ 4 in-corpus citations
Limited metadata. Only one source feed has indexed this record so far — no abstract, full text, or open-access copy is available through Endo Lab. The publisher's page (linked below) is the canonical location for the actual content. If you have institutional access, use "Find at my library".
AI-generated summary by claude@2026-06+body, 2026-06-07

Integrated transcriptomics identified BST2 as a potential diagnostic biomarker in endometriosis, with its overexpression promoted by TNF-α and potentially driving disease via the TNF-α/NF-κB pathway.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-06, 2026-06-07

This study used integrated transcriptomics on multiple public endometriosis expression datasets (34 normal, 127 eutopic, and 46 ectopic endometrium samples) followed by in vitro experiments in primary endometrial stromal cells to investigate mechanisms and biomarker candidates. Bioinformatic analyses highlighted dysregulated immune-inflammation and tissue remolding pathways, and among upregulated genes, BST2 was selected as a potential diagnostic biomarker associated with r-AFS stage and immune-inflammation processes; BST2 was also confirmed to be upregulated at RNA and protein levels in endometriosis tissues. TNF-α increased BST2 expression in stromal cells, and BST2 knockdown reduced migration, invasion, adhesion, and inflammatory readouts (while not affecting proliferation), suggesting involvement of the TNF-α/NF-κB pathway. This paper explicitly focuses on endometriosis (not adenomyosis) by identifying BST2 as a diagnostic/therapeutic target linked to TNF-α/NF-κB-driven immune-inflammation and tissue remodeling.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

My notes (saved in your browser only)

Condition tags

mesh:D004715endometriosis

MeSH descriptors

Antigens, CD Antigens, CD Antigens, CD Antigens, CD Antigens, CD Antigens, CD Antigens, CD Antigens, CD Antigens, CD Antigens, CD Antigens, CD Antigens, CD Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis Endometriosis

Citation neighborhood

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.

References (65)

Cited by (4)

Source provenance

europepmc
last seen: 2026-06-04T01:30:01.192114+00:00
openalex
last seen: 2026-06-10T17:14:06.276822+00:00
pubmed
last seen: 2026-05-27T00:32:57.245422+00:00
License: CC0 · commercial use OK