L1CAML1 Cell Adhesion Molecule
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Following DNA isolation from peripheral blood, molecular analysis of L1CAM gene (NM_000425) was performed using a targeted next generation sequencing panel (the TruSight Inherited Disease[R] panel).
The neural adhesion molecule L1CAM confers chemoresistance in human glioblastomas.
Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease.
Promising agents that have been shown to reduce fetal cell toxicity include anti-inflammatory agents such as prostaglandin inhibitors, growth factors, antioxidants, the nutrient choline, and agents that interfere with alcohol-related disruption of the L1CAM system (Yeaney et al.
4] Nonstandard abbreviations: PI3K, phosphoinositide 3-kinase; MSI, microsatellite instability; TCGA, The Cancer Genome Atlas; L1CAM, L1 cell adhesion molecule; EpCAM, epithelial cell adhesion molecule; IMP3, insulin-like growth factor 2 mRNA-binding protein 3; RTK, receptor tyrosine kinase.
In the comparative study with normal cells quoted above, (74) SEMA3C, ITGB4, CDH3, and COL6A1 were highly expressed in the epithelioid MPM subtype; L1CAM, K14, and INP10 were overexpressed in the mixed MPM subtype; and MMP9 and PLXN3 were overexpressed in the sarcomatoid MPM subtype.
L1CAM, INP10, P-cadherin, tPA and ITGB4 over-expression in malignant pleural mesotheliomas revealed by combined use of cDNA and tissue microarray.
The potential development of such agents recently has been enhanced by the identification of the alcohol-binding site on the L1CAM (Arevalo et al.
Charness and coworkers (1994) demonstrated that alcohol inhibits the adhesive properties of L1CAM in cell cultures, preventing neurons from properly adhering to each other or to the ECM.
67) The expression of L1CAM, COX2, and EGFR proteins in undifferentiated carcinomas have been noted as possible future targets of inhibitor-based treatments.