Solid pseudopapillary carcinoma of pancreas
diseaseOn this page
Also known as pancreatic solid pseudopapillary carcinomasolid pseudopapillary carcinoma of the pancreassolid pseudopapillary neoplasm of the pancreas
Summary
Solid pseudopapillary carcinoma of pancreas (MONDO:0018525) is a cancer with 1 cohort gene (1 CIViC-evidence somatic driver) and 4 clinical trials. Top therapeutic interventions include tegavivint.
At a glance
- Classification: Cancer
- Prevalence: <1 / 1 000 000 (Europe) [Orphanet-validated]
- Cohort genes: 1
- Clinical trials: 4
Clinical features
Epidemiology
Prevalence records
12 prevalence record(s), Orphanet:
| Type | Class | Value | Geography | Validation |
|---|---|---|---|---|
| Annual incidence | <1 / 1 000 000 | 0.003 | Europe | Validated |
| Annual incidence | <1 / 1 000 000 | 0.003 | Austria | Validated |
| Annual incidence | <1 / 1 000 000 | 0.008 | Belgium | Validated |
| Annual incidence | <1 / 1 000 000 | 0.003 | Croatia | Validated |
| Annual incidence | <1 / 1 000 000 | 0.011 | Czech Republic | Validated |
| Annual incidence | <1 / 1 000 000 | 0.005 | France | Validated |
| Annual incidence | <1 / 1 000 000 | 0.004 | Germany | Validated |
| Annual incidence | <1 / 1 000 000 | 0.005 | Italy | Validated |
| Annual incidence | <1 / 1 000 000 | 0.003 | Norway | Validated |
| Annual incidence | <1 / 1 000 000 | 0.009 | Spain | Validated |
| Annual incidence | <1 / 1 000 000 | 0.002 | Netherlands | Validated |
| Annual incidence | <1 / 1 000 000 | 0.001 | United Kingdom | Validated |
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | solid pseudopapillary carcinoma of pancreas |
| Mondo ID | MONDO:0018525 |
| Orphanet | 424065 |
| DOID | DOID:6827 |
| NCIT | C5728 |
| UMLS | C1336029 |
| MedGen | 236832 |
| GARD | 0021780 |
| Is cancer (heuristic) | yes |
Also known as: pancreatic solid pseudopapillary carcinoma · solid pseudopapillary carcinoma of pancreas · solid pseudopapillary carcinoma of the pancreas · solid pseudopapillary neoplasm of the pancreas
Disease family
Classification path: disease › human disease › disease by body system or component › digestive system disorder › digestive system cancer › malignant pancreatic neoplasm › malignant exocrine pancreas neoplasm › exocrine pancreatic carcinoma › solid pseudopapillary carcinoma of pancreas
Related subtypes (7): pancreatic intraductal papillary-mucinous carcinoma, pancreatic adenocarcinoma, pancreatic large cell neuroendocrine carcinoma, familial pancreatic carcinoma, squamous cell carcinoma of pancreas, pancreatic mucinous cystadenoma, pancreatic carcinoma with mixed differentiation
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
Mendelian disease overlap and somatic drivers
GenCC: 0 · Orphanet: 12 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0
Somatic driver evidence (intOGen + CIViC, cohort fanout)
| Gene | intOGen role | Cancer types | CIViC |
|---|---|---|---|
| CTNNB1 | Act | ACC,COAD,COADREAD,ESCA,HCC,LIHB,LUAD,MBL,MEL,NSCLC,OVT,PAST,PRAD,PROSTATE,RMS,SKIN,SOFT_TISSUE,STAD,UCEC,WT | CIViC #1290 |
Orphanet rare-disease linkage (cohort genes)
| Gene | Orphanet ID | Rare disease |
|---|---|---|
| CTNNB1 | Orphanet:1501 | Adrenocortical carcinoma |
| CTNNB1 | Orphanet:210159 | Adult hepatocellular carcinoma |
| CTNNB1 | Orphanet:2780 | Osteopathia striata-cranial sclerosis syndrome |
| CTNNB1 | Orphanet:33402 | Pediatric hepatocellular carcinoma |
| CTNNB1 | Orphanet:404473 | Intellectual disability-eye abnormalities-microcephaly-peripheral spasticity syndrome |
| CTNNB1 | Orphanet:54595 | Craniopharyngioma |
| CTNNB1 | Orphanet:569248 | Microcystic stromal tumor |
| CTNNB1 | Orphanet:689430 | Adenoid ameloblastoma |
| CTNNB1 | Orphanet:873 | Desmoid tumor |
| CTNNB1 | Orphanet:891 | Familial exudative vitreoretinopathy |
| CTNNB1 | Orphanet:91414 | Pilomatrixoma |
| CTNNB1 | Orphanet:952 | Acrofacial dysostosis, Weyers type |
Cohort genes → proteins
1 cohort genes, 1 distinct canonical proteins.
Evidence partition
| Subset | Genes |
|---|---|
| civic_only | 1 |
Cohort genes (full)
| Symbol | HGNC | Ensembl | UniProt | Name | Evidence |
|---|---|---|---|---|---|
| CTNNB1 | HGNC:2514 | ENSG00000168036 | P35222 | Catenin beta-1 | civic_evidence |
Cohort function summary
Lead sentence per gene, UniProt-curated.
| Symbol | Protein name | Function (lead sentence) |
|---|---|---|
| CTNNB1 | Catenin beta-1 | Key downstream component of the canonical Wnt signaling pathway. |
Protein-family classification
Druggable: 0 · Difficult: 0 · Unknown: 1 · Druggable fraction: 0.0
Family distribution
Cohort families vs a genome-wide background (hypergeometric, BH-FDR; fold = observed/expected). Counts kept; sorted by enrichment, so the catch-all Other/Unknown bucket no longer leads.
| Family | Genes | Fold | FDR |
|---|---|---|---|
| Other/Unknown | 1 | 1.8× | 0.558 |
Per-gene assignment
| Symbol | Family | Druggable? | EC | InterPro (top 3) |
|---|---|---|---|---|
| CTNNB1 | Other/Unknown | no | Armadillo, ARM-like, Beta-catenin |
Expression context
Cohort genes with no expression data: 0.
1 cohort gene are a single-cell marker in ≥1 SCXA experiment.
Breadth distribution (Bgee present_calls)
| Bucket | Genes |
|---|---|
| narrow (1-5 tissues) | 0 |
| moderate (6-20) | 0 |
| broad (>20) | 1 |
| unknown | 0 |
Top tissues across cohort
| Tissue | Cohort genes |
|---|---|
| adrenal tissue | 1 |
| periodontal ligament | 1 |
| ventricular zone | 1 |
Per-gene tissue summary (top 30)
| Symbol | Bgee breadth | FANTOM5 breadth | SCXA | Top tissues |
|---|---|---|---|---|
| CTNNB1 | 295 | ubiquitous | marker | adrenal tissue, ventricular zone, periodontal ligament |
Protein interactions among cohort
Intra-cohort edges: 0.
Hub genes (top 10 by interactor count)
| Symbol | Interactor count |
|---|---|
| CTNNB1 | 15,668 |
Structural data
PDB: 1 · AlphaFold-only: 0 · No structure: 0
Cohort genes with PDB structures (top 30)
| Symbol | UniProt | PDB entries |
|---|---|---|
| CTNNB1 | P35222 | 50 |
Function
Pathway analysis
Distinct Reactome pathways touched by cohort: 46. Enrichment computed across 1 evidence-associated genes (1 with Reactome annotation).
Pathways by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| Pathway | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production | 1 | 2284.0× | 0.004 | CTNNB1 |
| CDH11 homotypic and heterotypic interactions | 1 | 1631.4× | 0.004 | CTNNB1 |
| Regulation of CDH19 Expression and Function | 1 | 1427.5× | 0.004 | CTNNB1 |
| InlA-mediated entry of Listeria monocytogenes into host cells | 1 | 1268.9× | 0.004 | CTNNB1 |
| Binding of TCF/LEF:CTNNB1 to target gene promoters | 1 | 1142.0× | 0.004 | CTNNB1 |
| RUNX3 regulates WNT signaling | 1 | 1142.0× | 0.004 | CTNNB1 |
| Apoptotic cleavage of cell adhesion proteins | 1 | 1038.2× | 0.004 | CTNNB1 |
| Regulation of CDH11 function | 1 | 1038.2× | 0.004 | CTNNB1 |
| Regulation of CDH1 Function | 1 | 951.7× | 0.004 | CTNNB1 |
| Formation of axial mesoderm | 1 | 815.7× | 0.004 | CTNNB1 |
| Signaling by GSK3beta mutants | 1 | 761.3× | 0.004 | CTNNB1 |
| CTNNB1 S33 mutants aren’t phosphorylated | 1 | 761.3× | 0.004 | CTNNB1 |
| CTNNB1 S37 mutants aren’t phosphorylated | 1 | 761.3× | 0.004 | CTNNB1 |
| CTNNB1 S45 mutants aren’t phosphorylated | 1 | 761.3× | 0.004 | CTNNB1 |
| CTNNB1 T41 mutants aren’t phosphorylated | 1 | 761.3× | 0.004 | CTNNB1 |
| Formation of definitive endoderm | 1 | 713.8× | 0.004 | CTNNB1 |
| Beta-catenin phosphorylation cascade | 1 | 671.8× | 0.004 | CTNNB1 |
| Germ layer formation at gastrulation | 1 | 671.8× | 0.004 | CTNNB1 |
| Formation of the nephric duct | 1 | 634.4× | 0.004 | CTNNB1 |
| Specification of the neural plate border | 1 | 634.4× | 0.004 | CTNNB1 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | 1 | 571.0× | 0.004 | CTNNB1 |
| Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | 1 | 519.1× | 0.004 | CTNNB1 |
| SRC activates STAT3 in a quantitative manner, through Cadherin-11 (CDH11), RAC1 and gp130 (IL6ST) | 1 | 496.5× | 0.004 | CTNNB1 |
| Cardiogenesis | 1 | 423.0× | 0.004 | CTNNB1 |
| VEGFR2 mediated vascular permeability | 1 | 407.9× | 0.004 | CTNNB1 |
| Formation of paraxial mesoderm | 1 | 407.9× | 0.004 | CTNNB1 |
| Myogenesis | 1 | 380.7× | 0.004 | CTNNB1 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | 1 | 356.9× | 0.005 | CTNNB1 |
| RHO GTPases activate IQGAPs | 1 | 346.1× | 0.005 | CTNNB1 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | 1 | 335.9× | 0.005 | CTNNB1 |
GO biological processes by enrichment
Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.
| GO term | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| glial cell fate determination | 1 | 16852.0× | 0.001 | CTNNB1 |
| canonical Wnt signaling pathway involved in mesenchymal stem cell differentiation | 1 | 16852.0× | 0.001 | CTNNB1 |
| cranial ganglion development | 1 | 16852.0× | 0.001 | CTNNB1 |
| neural plate development | 1 | 8426.0× | 0.001 | CTNNB1 |
| negative regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis | 1 | 8426.0× | 0.001 | CTNNB1 |
| regulation of centriole-centriole cohesion | 1 | 8426.0× | 0.001 | CTNNB1 |
| negative regulation of mitotic cell cycle, embryonic | 1 | 8426.0× | 0.001 | CTNNB1 |
| regulation of timing of anagen | 1 | 8426.0× | 0.001 | CTNNB1 |
| positive regulation of branching involved in lung morphogenesis | 1 | 8426.0× | 0.001 | CTNNB1 |
| renal vesicle formation | 1 | 8426.0× | 0.001 | CTNNB1 |
| renal inner medulla development | 1 | 8426.0× | 0.001 | CTNNB1 |
| renal outer medulla development | 1 | 8426.0× | 0.001 | CTNNB1 |
| nephron tubule formation | 1 | 8426.0× | 0.001 | CTNNB1 |
| regulation of nephron tubule epithelial cell differentiation | 1 | 8426.0× | 0.001 | CTNNB1 |
| mesenchymal stem cell differentiation | 1 | 8426.0× | 0.001 | CTNNB1 |
| positive regulation of determination of dorsal identity | 1 | 8426.0× | 0.001 | CTNNB1 |
| astrocyte-dopaminergic neuron signaling | 1 | 5617.3× | 0.001 | CTNNB1 |
| regulation of fibroblast proliferation | 1 | 5617.3× | 0.001 | CTNNB1 |
| oviduct development | 1 | 5617.3× | 0.001 | CTNNB1 |
| lung induction | 1 | 5617.3× | 0.001 | CTNNB1 |
| positive regulation of epithelial cell proliferation involved in prostate gland development | 1 | 5617.3× | 0.001 | CTNNB1 |
| fungiform papilla formation | 1 | 5617.3× | 0.001 | CTNNB1 |
| regulation of centromeric sister chromatid cohesion | 1 | 5617.3× | 0.001 | CTNNB1 |
| regulation of secondary heart field cardioblast proliferation | 1 | 4213.0× | 0.001 | CTNNB1 |
| metanephros morphogenesis | 1 | 4213.0× | 0.001 | CTNNB1 |
| positive regulation of heparan sulfate proteoglycan biosynthetic process | 1 | 4213.0× | 0.001 | CTNNB1 |
| embryonic skeletal limb joint morphogenesis | 1 | 4213.0× | 0.001 | CTNNB1 |
| central nervous system vasculogenesis | 1 | 3370.4× | 0.001 | CTNNB1 |
| genitalia morphogenesis | 1 | 3370.4× | 0.001 | CTNNB1 |
| epithelial cell differentiation involved in prostate gland development | 1 | 3370.4× | 0.001 | CTNNB1 |
Therapeutics
Drug target analysis
Approved (phase 4): 1 · Phase ≥3: 1 · Phased (≥1): 1 · Undrugged: 0
Druggability breadth: 1 of 1 evidence-associated genes (100%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).
Genes with an approved drug
The molecule shown is one approved compound that hits the gene — not necessarily a drug of choice or one indicated for this disease.
| Symbol | Example approved molecule |
|---|---|
| CTNNB1 | DITHIAZANINE IODIDE |
Top cohort targets by molecule count
| Symbol | Molecules | Max phase |
|---|---|---|
| CTNNB1 | 4 | 4 |
Drugs targeting cohort genes (top 30)
| Molecule | Max phase | Targets in cohort |
|---|---|---|
| DITHIAZANINE IODIDE | 4 | CTNNB1 |
| QUERCETIN | 3 | CTNNB1 |
| SALINOMYCIN | 2 | CTNNB1 |
| DALOSIRVAT | 2 | CTNNB1 |
Bioactivity and enzyme data
Enzyme cohort genes (≥1 EC): 0.
Cohort genes with ChEMBL bioactivity (full, sorted by assay count)
| Symbol | Assays | Type breakdown |
|---|---|---|
| CTNNB1 | 361 | Binding:358, Functional:3 |
Cohort genes with high screening signal
≥100 ChEMBL assays — a studied-ness signal; see Therapeutics for approved-drug status.
| Symbol | ChEMBL assays |
|---|---|
| CTNNB1 | 361 |
Pharmacogenomics
Cohort genes with a PharmGKB record: 1; with CPIC/DPWG dosing guidelines: 0.
No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).
Drug repurposing candidates
4 approved/phased drugs hit cohort targets but don’t yet appear in disease-level clinical trials. Target-inhibition rationale is strongest for cancer driver genes; a bioactivity hit is a screening signal, not a treatment claim.
| Compound | Max phase | Cohort target (bioactivity) |
|---|---|---|
| DITHIAZANINE IODIDE | 4 | CTNNB1 |
| QUERCETIN | 3 | CTNNB1 |
| SALINOMYCIN | 2 | CTNNB1 |
| DALOSIRVAT | 2 | CTNNB1 |
Druggability pyramid
Cohort genes binned by druggability tier (high → low):
| Tier | Definition | Genes | Symbols |
|---|---|---|---|
| A | Approved (phase 4 drug) | 1 | CTNNB1 |
| B | Phased (≥1) drug, not yet approved | 0 | |
| C | Druggable family + PDB, no drug | 0 | |
| D | Druggable family + AlphaFold only, no drug | 0 | |
| E | Difficult family or no structure, no drug | 0 |
Undrugged target profiles
0 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).
Clinical trials & evidence
Clinical trials
Clinical trials: 4.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 3 |
| PHASE1/PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04851119 | PHASE1/PHASE2 | RECRUITING | Tegavivint for the Treatment of Recurrent or Refractory Solid Tumors, Including Lymphomas and Desmoid Tumors |
| NCT06753318 | Not specified | NOT_YET_RECRUITING | Validation of Joint-AI in Diagnosing Pancreatic Solid Lesions |
| NCT07183280 | Not specified | RECRUITING | Multicentric Database for Solid Pseudopapillary Neoplasm of the Pancreas |
| NCT04728750 | Not specified | COMPLETED | Laparoscopic Enucleation of Frantz’s Tumor of the Pancreas |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| TEGAVIVINT | 2 | 1 |
| CHEMBL6083129 | 0 | 1 |
Related Atlas pages
- Cohort genes: CTNNB1