Drug pipeline
Full profile accessExplore the programs pursuing this target and their development progress.
- Drug candidates
- Developers
- Development stage
Target intelligence / Profile preview
SENP3-EIF4A1 is a long non-coding RNA formed by readthrough transcription or a fusion event between the SUMO-specific peptidase 3 (SENP3) and Eukaryotic translation initiation factor 4A1 (EIF4A1) genes located on chromosome 17. This transcript is typically targeted for nonsense-mediated decay and does not encode a functional protein. Recent research implicates SENP3-EIF4A1 as a competing endogenous RNA (ceRNA) in triple-negative breast cancer, where it acts as a sponge for miR-195-5p and regulates expression of Cyclin E1 (CCNE1), thereby promoting cell proliferation and cancer progression. Its expression correlates with poor prognosis in TNBC. The molecule is being investigated as a potential diagnostic biomarker and therapeutic target, especially as part of the SENP3-EIF4A1/miR-195-5p/CCNE1 axis, but its full biological function and disease spectrum remain incompletely characterized.
For 5-Aza-DC: Demethylation leads to upregulation of miR-195-5p, which downregulates CCNE1 expression, disrupting the oncogenic SENP3-EIF4A1/miR-195-5p/CCNE1 axis
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Explore the programs pursuing this target and their development progress.
Follow the clinical studies evaluating therapies directed at this target.
Compare approaches across drug candidates, modalities, and indications.
Investigate the research and source evidence behind target biology and development.
Explore patent activity around therapies and technologies addressing this target.
Connect target biology, drug development, and emerging evidence in your research.
See how Gosset can support your research on SENP3-EIF4A1 readthrough (NMD candidate) (SENP3-EIF4A1).