| 2003 |
Purified recombinant human PAOh1/SMO (SMOX) is a flavin-dependent polyamine oxidase that oxidizes spermine (Km=1.6 µM) and N1-acetylspermine (Km=51 µM) but does not oxidize spermidine; specific oligamine analogues are potent inhibitors of spermine oxidation by PAOh1/SMO. |
In vitro enzymatic assay with purified recombinant protein; substrate kinetics determination; inhibitor screening |
Biochemical and biophysical research communications |
High |
12727196
|
| 2005 |
In polyamine analogue (BENSpm)-treated human breast cancer cells, SMO(PAOh1)/SMOX—not the peroxisomal acetylpolyamine oxidase PAO—is the exclusive source of cytotoxic H2O2 produced through polyamine catabolism; stable siRNA knockdown of SMOX rendered MDA-MB-231 cells significantly resistant to BENSpm-induced growth inhibition. |
Stable siRNA knockdown; H2O2 measurement; cell growth and polyamine pool assays; enzyme activity assays |
The Journal of biological chemistry |
High |
16207710
|
| 2003 |
PAOh1/SMO (SMOX) is induced at the mRNA and activity level by multiple antitumor polyamine analogues in human lung carcinoma cell lines, with the most potent inducers possessing multiple three-carbon linkers between nitrogens (e.g., N1,N11-bis(ethyl)norspermine). |
mRNA expression analysis; enzyme activity assays; analogue structure-activity comparison across cell lines |
Cancer chemotherapy and pharmacology |
Medium |
12827295
|
| 2005 |
Analogue (CPENSpm)-induced expression of SMOX is regulated at the levels of new mRNA synthesis, mRNA stabilization (half-life increased from ~8.8 h to ~17.1 h upon treatment), and newly synthesized protein, with a 30–90% increase in transcription demonstrated by promoter reporter constructs; protein stabilization does not play a significant role. |
Actinomycin D mRNA half-life assays; cycloheximide protein synthesis inhibition; promoter reporter constructs; enzyme activity assays |
The Biochemical journal |
High |
15496143
|
| 2019 |
SMOX downregulation by AAV-mediated RNAi in a rat MCAO model significantly reduced brain infarct volume, neuronal apoptosis, and inflammatory reactions (IL-6, TNF-α); neurons with reduced SMOX after OGD/R produced conditioned medium that caused less microglial activation, implicating SMOX-derived H2O2/oxidative products as mediators of neuroinflammatory signaling. |
AAV-RNAi knockdown in vivo (MCAO rat model); OGD/R primary neuron culture; conditioned medium transfer to microglia; cytokine measurement; infarct volume quantification |
Toxicological sciences |
Medium |
30576531
|
| 2022 |
Novel small-molecule SMOX inhibitors (compounds 6 and 7) with IC50 values of 0.54 µM and 0.23 µM, and Ki values of 1.60 µM and 0.46 µM respectively, were identified via virtual and physical screening, demonstrating that SMOX enzymatic activity is pharmacologically targetable with high selectivity. |
Virtual screening; in vitro enzyme inhibition assays (IC50, Ki determination); selectivity profiling |
Medical sciences (Basel, Switzerland) |
Medium |
36135832
|
| 2023 |
Knockdown of SMOX with siRNA lentivirus in the tMCAO stroke model protected blood-brain barrier integrity by reducing oxidative stress and activating the Nrf2 pathway; blocking Nrf2 with brusatol abolished the protective effects, placing SMOX-mediated H2O2 production upstream of Nrf2 suppression in BBB endothelial cells. |
siRNA lentivirus knockdown in vivo (tMCAO mouse model) and in vitro (bEnd.3 cells); Nrf2 pathway inhibition with brusatol; BBB permeability assays; oxidative stress markers; apoptosis markers |
International immunopharmacology |
Medium |
37984250
|
| 2025 |
SMOX promotes hepatocellular carcinoma cell proliferation, migration, and invasion by activating the AKT-mTOR signaling pathway and epithelial-mesenchymal transition (EMT); SMOX overexpression increased phosphorylation of AKT, mTOR, and downstream effectors, and upregulated EMT markers (N-cadherin, vimentin, Snail) while downregulating E-cadherin. miR-139-5p directly targets SMOX (confirmed by dual-luciferase assay) and suppresses this pathway. |
Dual-luciferase reporter assay (miR-139-5p targeting SMOX 3'UTR); Western blotting for pathway phosphorylation; overexpression and knockdown functional assays; rescue experiments |
Scientific reports |
Medium |
41444797
|
| 2026 |
SMOX elevates intracellular ROS, which transcriptionally upregulates the pseudokinase TRIB3; TRIB3 interacts with and suppresses GSK-3β activity, thereby stabilizing β-catenin and activating the Wnt/β-catenin pathway in colorectal cancer. ZNF263 was identified as a transcriptional activator of SMOX by directly binding the SMOX promoter (ChIP-qPCR). SMOX knockdown suppressed proliferation, migration, invasion, and peritoneal metastasis in vivo. |
Co-IP (TRIB3-GSK-3β interaction); ChIP-qPCR (ZNF263 binding to SMOX promoter); Western blotting; ROS measurement; in vivo xenograft and peritoneal metastasis models; SMOX knockdown/overexpression functional assays |
Apoptosis |
Medium |
42262434
|
| 2025 |
PUS1 stabilizes SMOX mRNA via pseudouridylation, promoting ccRCC cell migration; PUS1 silencing reduced cell migration, while overexpression increased it. The upstream transcription factor USF1 regulates PUS1 expression by binding to its promoter. |
PUS1 knockdown/overexpression in ccRCC cell lines; migration assays; mRNA pseudouridylation analysis; promoter binding assay for USF1 |
Cellular signalling |
Medium |
39993614
|
| 2025 |
In a Drosophila model of Parkinson's disease overexpressing human α-synuclein, RNAi knockdown of SMOX significantly affected fly lifespan and motility; overexpression of SMOX had positive enduring effects on lifespan and altered α-synuclein protein levels, implicating SMOX-mediated polyamine catabolism in modulation of α-synuclein levels. |
RNAi knockdown and transgenic overexpression in Drosophila PD model; lifespan and motility assays; α-synuclein protein level measurement |
bioRxivpreprint |
Low |
bio_10.1101_2025.03.06.641237
|
| 2025 |
Pharmacological inhibition of SMOX (in vivo) significantly alleviated tubular injury, preserved renal function, and reduced oxidative stress in acute kidney injury; in vitro SMOX inhibition maintained epithelial cell integrity and viability while suppressing oxidative damage in renal tubular cells. |
Pharmacological SMOX inhibition in vivo (AKI model) and in vitro (renal tubular cells); functional readouts (tubular injury markers, renal function, oxidative stress markers, cell viability) |
International journal of biological macromolecules |
Low |
40683494
|
| 2026 |
SMOX silencing in rheumatoid arthritis fibroblast-like synoviocytes (RA-FLS) inhibited migration, invasion, and cytokine production while inducing apoptosis; pharmacological SMOX inhibition with JNJ-9350 produced comparable anti-inflammatory effects in vitro and reduced arthritis severity in collagen antibody-induced arthritis (CAIA) mice in vivo. |
SMOX siRNA knockdown in RA-FLS; pharmacological inhibition with JNJ-9350 in vitro and in vivo (CAIA mouse model); migration/invasion assays; cytokine measurement; histopathological analysis |
Molecular immunology |
Medium |
41485416
|