Target intelligence / Profile preview

Staphylococcal nuclease domain-containing protein 1 (SND1) (SND1)

Target
SND1
Molecular classification
Enzyme, Transcriptional coactivator, Nuclease, RNA-binding protein
01

Overview

Staphylococcal nuclease domain-containing protein 1 (SND1), also known as Tudor-SN or p100, is a multifunctional protein that plays a critical role in gene expression regulation at both transcriptional and post-transcriptional levels (UniProt KB - Q7KZF4). It is characterized by four staphylococcal nuclease (SN) domains and a Tudor domain, which facilitate its interactions with DNA, RNA, and proteins (PubMed: 24510034). SND1 acts as a transcriptional coactivator and is a key component of the RNA-induced silencing complex (RISC), where it promotes the degradation of hyper-edited miRNA precursors (PubMed: 30143548). In oncology, SND1 is frequently overexpressed and correlates with poor prognosis in various malignancies, including hepatocellular carcinoma and colon cancer, by promoting cell proliferation, metastasis, and chemoresistance (PubMed: 24510034). Therapeutic strategies focus on small molecule inhibitors that target the active site of the SN domains to block its nuclease activity and protein-protein interactions (PubMed: 25103497). While no drugs are currently FDA-approved, experimental inhibitors like 3',5'-deoxythymidine bisphosphate (pdTp) and its derivatives have shown promise in preclinical models by disrupting the oncogenic signaling pathways mediated by SND1 (PubMed: 25103497).

Other names
Tudor-SNp100Tudor domain-containing protein 11TDRD11100 kDa coactivator
02

Mechanism of action

Competitive inhibition of the staphylococcal nuclease (SN) domain active site, which prevents RNA binding and cleavage, thereby disrupting the RNA-induced silencing complex (RISC) and oncogenic transcriptional coactivation.

03

Biological functions

Transcription regulationRNA interferencemRNA splicingmRNA degradationStress granule formationRNA-induced silencing complex (RISC) activity
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Disease associations

CancerHepatocellular carcinomaColon cancerBreast cancerProstate cancerInflammation
05

Safety considerations

Potential disruption of normal RNA metabolism and mRNA stabilityImpairment of cellular stress response due to role in stress granule formationPotential off-target effects on other cellular nucleases
06

Interacting drugs

3',5'-deoxythymidine bisphosphate (pdTp)

2 more in the full profile.

07

Biomarkers

SND1 protein expression levelsSND1 mRNA levelsmiR-221 expression

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