mProX™ Human EPHB3 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 EphB3 exhibits ligand-induced inhibition of NSCLC cell migration.
EphB3 overexpression in an ectopic manner in three NSCLC cell lines (H520, H23, and A549, in that order). After three days of puromycin selection, cells were infected with lentiviruses expressing either HA-EphB3 or vector control.
Ref: Li, Guo, et al. "EphB3 suppresses non-small-cell lung cancer metastasis via a PP2A/RACK1/Akt signalling complex." Nature communications 3.1 (2012): 667.
Pubmed: 22314363
DOI: 10.1038/ncomms1675
Research Highlights
Human hepatocellular carcinoma (Eph) receptor tyrosine kinases (RTKs) that produce erythropoietin regulate a number of dynamic cellular processes, such as cell motility, protrusion, proliferation, and cell-fate determination. Eph kinase small-molecule inhibitors are useful instruments for analyzing the physiological and pathological functions of Eph.
Kung, Alvin, et al. "Development of specific, irreversible inhibitors for a receptor tyrosine kinase EphB3." Journal of the American Chemical Society 138.33 (2016): 10554-10560.
Pubmed:
27478969
DOI:
10.1021/jacs.6b05483
These findings suggest that EphB3 may act as a limiter on bone formation and identify it as a potential regulator of osteogenesis, either by itself or in conjunction with other bone-expressed Ephs.
Kamath, Rajay AD, and M. Douglas Benson. "EphB3 as a potential mediator of developmental and reparative osteogenesis." Cells Tissues Organs 212.2 (2023): 125-137.
Pubmed:
34695818
DOI:
10.1159/000520369