Basic information
Biomarker: L1CAM
Histology type: endometrial carcinoma
Cohort characteristics
Country: Netherlands/UK/Canada/Australia/France
Region: collaborating institutions within the TransPORTEC consortium.
Study type: Multicenter Study
Followed up time :
Subgroup 1 name : <10%
Subgroup 1 number: 65
Subgroup 2 name: ≥10%
Subgroup 2 number: 51
Total number | Group I | Group I number | Group II | Group II number | Group III | Group III number | Group IV | Group IV number |
---|---|---|---|---|---|---|---|---|
116 | endometrioid endometrial cancer | 86 | non-endometrioid subtype | 30 |
Sample information
Conclusion: The high frequency of L1CAM expression in high-risk endometrial cancers suggests that it may also be a promising therapeutic target in this tumor subset.
Sample type : tissue
Sample method: immunohistochemistry
Expression pattern : threshold (>50%)
Expression elevation: The percentage of positive membranous L1CAM staining within the tumor was scored as 0%, <10%, 10–50%, or >50%, according to a recently published scoring system for endometrial cancer. If the tumor stained >10%, it was considered L1CAM-positive, based on prior studies.
Disease information
Statictics: Mean
Cohort age: 66.3
Subgroup 1 age: 64.3
Subgroup 2 age: 68.7
Related information
Funtion Uniprot: Neural cell adhesion molecule involved in the dynamics of cell adhesion and in the generation of transmembrane signals at tyrosine kinase receptors. During brain development, critical in multiple processes, including neuronal migration, axonal growth and fasciculation, and synaptogenesis. In the mature brain, plays a role in the dynamics of neuronal structure and function, including synaptic plasticity.
UniProt ID: P32004
UniProt Link: https://www.uniprot.org/uniprotkb/P32004/entry
Biological function from UniProt: #Cell adhesion #Differentiation #Neurogenesis
Molecular function from UniProt:
Subcellular UniProt: #Cell membrane #Cell projection #Membrane
Recommended name: Neural cell adhesion molecule L1
Gene name from HGNC: L1CAM (CD171, HSAS, HSAS1, MASA, MIC5, S10, SPG1)
CD antigen name: CD171
HPA class: CD markers Disease related genes Human disease related genes Metabolic proteins Plasma proteins
AlphaFold DB: P32004
AlphaFold Link: https://alphafold.ebi.ac.uk/entry/P32004
HPA link: https://www.proteinatlas.org/ENSG00000198910-L1CAM
Tissue specificity RNA from HPA: Tissue enhanced (brain, intestine)
Tissue expression from HPA: Cytoplasmic expression mainly in CNS, PNS and distal renal tubules.
Single cell type specificity Cell type enhanced (Collecting duct cells, Melanocytes, Horizontal cells, Excitatory neurons, Inhibitory neurons)
Immune cell specificity: Not detected in immune cells
Subcellular summary HPA Located in Nucleoplasm, Plasma membrane (Single cell variability)
Cancer prognostic summary HPA Prognostic marker in endometrial cancer (unfavorable), lung cancer (unfavorable), renal cancer (unfavorable) and head and neck cancer (unfavorable)
Pathology link: https://www.proteinatlas.org/ENSG00000198910-L1CAM/pathology
Pathology endo: https://www.proteinatlas.org/ENSG00000198910-L1CAM/pathology/endometrial+cancer
Expression figure legend: Immunohistochemical stainings of p53 (left column) and L1 cell adhesion molecule (L1CAM)
Expression figure link: https://www.nature.com/articles/modpathol2015147/figures/2
Survival figure legend: Prognostic significance of L1CAM expression and its association with mutant p53 expression in high-risk endometrial cancer
Survival curve link: https://www.nature.com/articles/modpathol2015147/figures/1
Phenotype ID: 307000;303350;304100;
Disease: Hydrocephalus due to stenosis of the aqueduct of Sylvius (HSAS);MASA syndrome (MASA);Defects in L1CAM may contribute to Hirschsprung disease by modifying the effects of Hirschsprung disease-associated genes to cause intestinal aganglionosis; Defects in L1CAM are associated with a wide phenotypic spectrum which varies from severe hydrocephalus and prenatal death (HSAS) to a milder phenotype (MASA). These variations may even occur within the same family. Due to the overlap of phenotypes between HSAS and MASA, many authors use the general concept of L1 syndrome which covers both ends of the spectrum;
OMIM: 308840
OMIM link2: https://www.omim.org/entry/308840
HGNC ID: HGNC:6470
HGNC link: https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:6470