Solid pseudopapillary carcinoma of pancreas

disease
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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:

TypeClassValueGeographyValidation
Annual incidence<1 / 1 000 0000.003EuropeValidated
Annual incidence<1 / 1 000 0000.003AustriaValidated
Annual incidence<1 / 1 000 0000.008BelgiumValidated
Annual incidence<1 / 1 000 0000.003CroatiaValidated
Annual incidence<1 / 1 000 0000.011Czech RepublicValidated
Annual incidence<1 / 1 000 0000.005FranceValidated
Annual incidence<1 / 1 000 0000.004GermanyValidated
Annual incidence<1 / 1 000 0000.005ItalyValidated
Annual incidence<1 / 1 000 0000.003NorwayValidated
Annual incidence<1 / 1 000 0000.009SpainValidated
Annual incidence<1 / 1 000 0000.002NetherlandsValidated
Annual incidence<1 / 1 000 0000.001United KingdomValidated

Identifiers

Disease identifiers

FieldValue
Canonical namesolid pseudopapillary carcinoma of pancreas
Mondo IDMONDO:0018525
Orphanet424065
DOIDDOID:6827
NCITC5728
UMLSC1336029
MedGen236832
GARD0021780
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 disorderdigestive system cancermalignant pancreatic neoplasmmalignant exocrine pancreas neoplasmexocrine pancreatic carcinomasolid 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)

GeneintOGen roleCancer typesCIViC
CTNNB1ActACC,COAD,COADREAD,ESCA,HCC,LIHB,LUAD,MBL,MEL,NSCLC,OVT,PAST,PRAD,PROSTATE,RMS,SKIN,SOFT_TISSUE,STAD,UCEC,WTCIViC #1290

Orphanet rare-disease linkage (cohort genes)

GeneOrphanet IDRare disease
CTNNB1Orphanet:1501Adrenocortical carcinoma
CTNNB1Orphanet:210159Adult hepatocellular carcinoma
CTNNB1Orphanet:2780Osteopathia striata-cranial sclerosis syndrome
CTNNB1Orphanet:33402Pediatric hepatocellular carcinoma
CTNNB1Orphanet:404473Intellectual disability-eye abnormalities-microcephaly-peripheral spasticity syndrome
CTNNB1Orphanet:54595Craniopharyngioma
CTNNB1Orphanet:569248Microcystic stromal tumor
CTNNB1Orphanet:689430Adenoid ameloblastoma
CTNNB1Orphanet:873Desmoid tumor
CTNNB1Orphanet:891Familial exudative vitreoretinopathy
CTNNB1Orphanet:91414Pilomatrixoma
CTNNB1Orphanet:952Acrofacial dysostosis, Weyers type

Cohort genes → proteins

1 cohort genes, 1 distinct canonical proteins.

Evidence partition

SubsetGenes
civic_only1

Cohort genes (full)

SymbolHGNCEnsemblUniProtNameEvidence
CTNNB1HGNC:2514ENSG00000168036P35222Catenin beta-1civic_evidence

Cohort function summary

Lead sentence per gene, UniProt-curated.

SymbolProtein nameFunction (lead sentence)
CTNNB1Catenin beta-1Key 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.

FamilyGenesFoldFDR
Other/Unknown11.8×0.558

Per-gene assignment

SymbolFamilyDruggable?ECInterPro (top 3)
CTNNB1Other/UnknownnoArmadillo, 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)

BucketGenes
narrow (1-5 tissues)0
moderate (6-20)0
broad (>20)1
unknown0

Top tissues across cohort

TissueCohort genes
adrenal tissue1
periodontal ligament1
ventricular zone1

Per-gene tissue summary (top 30)

SymbolBgee breadthFANTOM5 breadthSCXATop tissues
CTNNB1295ubiquitousmarkeradrenal tissue, ventricular zone, periodontal ligament

Protein interactions among cohort

Intra-cohort edges: 0.

Hub genes (top 10 by interactor count)

SymbolInteractor count
CTNNB115,668

Structural data

PDB: 1 · AlphaFold-only: 0 · No structure: 0

Cohort genes with PDB structures (top 30)

SymbolUniProtPDB entries
CTNNB1P3522250

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.

PathwayCohort genesFoldFDRSample cohort genes
LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production12284.0×0.004CTNNB1
CDH11 homotypic and heterotypic interactions11631.4×0.004CTNNB1
Regulation of CDH19 Expression and Function11427.5×0.004CTNNB1
InlA-mediated entry of Listeria monocytogenes into host cells11268.9×0.004CTNNB1
Binding of TCF/LEF:CTNNB1 to target gene promoters11142.0×0.004CTNNB1
RUNX3 regulates WNT signaling11142.0×0.004CTNNB1
Apoptotic cleavage of cell adhesion proteins11038.2×0.004CTNNB1
Regulation of CDH11 function11038.2×0.004CTNNB1
Regulation of CDH1 Function1951.7×0.004CTNNB1
Formation of axial mesoderm1815.7×0.004CTNNB1
Signaling by GSK3beta mutants1761.3×0.004CTNNB1
CTNNB1 S33 mutants aren’t phosphorylated1761.3×0.004CTNNB1
CTNNB1 S37 mutants aren’t phosphorylated1761.3×0.004CTNNB1
CTNNB1 S45 mutants aren’t phosphorylated1761.3×0.004CTNNB1
CTNNB1 T41 mutants aren’t phosphorylated1761.3×0.004CTNNB1
Formation of definitive endoderm1713.8×0.004CTNNB1
Beta-catenin phosphorylation cascade1671.8×0.004CTNNB1
Germ layer formation at gastrulation1671.8×0.004CTNNB1
Formation of the nephric duct1634.4×0.004CTNNB1
Specification of the neural plate border1634.4×0.004CTNNB1
Regulation of MITF-M-dependent genes involved in cell cycle and proliferation1571.0×0.004CTNNB1
Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1)1519.1×0.004CTNNB1
SRC activates STAT3 in a quantitative manner, through Cadherin-11 (CDH11), RAC1 and gp130 (IL6ST)1496.5×0.004CTNNB1
Cardiogenesis1423.0×0.004CTNNB1
VEGFR2 mediated vascular permeability1407.9×0.004CTNNB1
Formation of paraxial mesoderm1407.9×0.004CTNNB1
Myogenesis1380.7×0.004CTNNB1
Disassembly of the destruction complex and recruitment of AXIN to the membrane1356.9×0.005CTNNB1
RHO GTPases activate IQGAPs1346.1×0.005CTNNB1
Regulation of CDH1 posttranslational processing and trafficking to plasma membrane1335.9×0.005CTNNB1

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 termCohort genesFoldFDRSample cohort genes
glial cell fate determination116852.0×0.001CTNNB1
canonical Wnt signaling pathway involved in mesenchymal stem cell differentiation116852.0×0.001CTNNB1
cranial ganglion development116852.0×0.001CTNNB1
neural plate development18426.0×0.001CTNNB1
negative regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis18426.0×0.001CTNNB1
regulation of centriole-centriole cohesion18426.0×0.001CTNNB1
negative regulation of mitotic cell cycle, embryonic18426.0×0.001CTNNB1
regulation of timing of anagen18426.0×0.001CTNNB1
positive regulation of branching involved in lung morphogenesis18426.0×0.001CTNNB1
renal vesicle formation18426.0×0.001CTNNB1
renal inner medulla development18426.0×0.001CTNNB1
renal outer medulla development18426.0×0.001CTNNB1
nephron tubule formation18426.0×0.001CTNNB1
regulation of nephron tubule epithelial cell differentiation18426.0×0.001CTNNB1
mesenchymal stem cell differentiation18426.0×0.001CTNNB1
positive regulation of determination of dorsal identity18426.0×0.001CTNNB1
astrocyte-dopaminergic neuron signaling15617.3×0.001CTNNB1
regulation of fibroblast proliferation15617.3×0.001CTNNB1
oviduct development15617.3×0.001CTNNB1
lung induction15617.3×0.001CTNNB1
positive regulation of epithelial cell proliferation involved in prostate gland development15617.3×0.001CTNNB1
fungiform papilla formation15617.3×0.001CTNNB1
regulation of centromeric sister chromatid cohesion15617.3×0.001CTNNB1
regulation of secondary heart field cardioblast proliferation14213.0×0.001CTNNB1
metanephros morphogenesis14213.0×0.001CTNNB1
positive regulation of heparan sulfate proteoglycan biosynthetic process14213.0×0.001CTNNB1
embryonic skeletal limb joint morphogenesis14213.0×0.001CTNNB1
central nervous system vasculogenesis13370.4×0.001CTNNB1
genitalia morphogenesis13370.4×0.001CTNNB1
epithelial cell differentiation involved in prostate gland development13370.4×0.001CTNNB1

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.

SymbolExample approved molecule
CTNNB1DITHIAZANINE IODIDE

Top cohort targets by molecule count

SymbolMoleculesMax phase
CTNNB144

Drugs targeting cohort genes (top 30)

MoleculeMax phaseTargets in cohort
DITHIAZANINE IODIDE4CTNNB1
QUERCETIN3CTNNB1
SALINOMYCIN2CTNNB1
DALOSIRVAT2CTNNB1

Bioactivity and enzyme data

Enzyme cohort genes (≥1 EC): 0.

Cohort genes with ChEMBL bioactivity (full, sorted by assay count)

SymbolAssaysType breakdown
CTNNB1361Binding:358, Functional:3

Cohort genes with high screening signal

≥100 ChEMBL assays — a studied-ness signal; see Therapeutics for approved-drug status.

SymbolChEMBL assays
CTNNB1361

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.

CompoundMax phaseCohort target (bioactivity)
DITHIAZANINE IODIDE4CTNNB1
QUERCETIN3CTNNB1
SALINOMYCIN2CTNNB1
DALOSIRVAT2CTNNB1

Druggability pyramid

Cohort genes binned by druggability tier (high → low):

TierDefinitionGenesSymbols
AApproved (phase 4 drug)1CTNNB1
BPhased (≥1) drug, not yet approved0
CDruggable family + PDB, no drug0
DDruggable family + AlphaFold only, no drug0
EDifficult family or no structure, no drug0

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)

PhaseTrials
Not specified3
PHASE1/PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04851119PHASE1/PHASE2RECRUITINGTegavivint for the Treatment of Recurrent or Refractory Solid Tumors, Including Lymphomas and Desmoid Tumors
NCT06753318Not specifiedNOT_YET_RECRUITINGValidation of Joint-AI in Diagnosing Pancreatic Solid Lesions
NCT07183280Not specifiedRECRUITINGMulticentric Database for Solid Pseudopapillary Neoplasm of the Pancreas
NCT04728750Not specifiedCOMPLETEDLaparoscopic Enucleation of Frantz’s Tumor of the Pancreas

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
TEGAVIVINT21
CHEMBL608312901