mProX™ Human AXL Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Expression of Axl in malignant glioma cells.
Three neuroblastoma cell lines (JMR32, SKSNH, and SHSY5Y) and one medulloblastoma cell line (TE671) were nonglial, neoplastic cell lines in which Axl mRNA expression levels were not increased. Northern analysis verified the findings obtained from the array analysis.
Ref: Vajkoczy, Peter, et al. "Dominant-negative inhibition of the Axl receptor tyrosine kinase suppresses brain tumor cell growth and invasion and prolongs survival." Proceedings of the National Academy of Sciences 103.15 (2006): 5799-5804.
Pubmed: 16585512
DOI: 10.1073/pnas.0510923103
Research Highlights
These findings suggest that AXL is expressed preferentially in tumor cells that are resistant to treatment, and that cotargeting AXL in this situation may be able to overcome medication resistance. In the clinic, AXL inhibitor use must to be taken into consideration.
Scaltriti, Maurizio, Moshe Elkabets, and José Baselga. "Molecular pathways: AXL, a membrane receptor mediator of resistance to therapy." Clinical Cancer Research 22.6 (2016): 1313-1317.
Pubmed:
26763248
DOI:
10.1158/1078-0432.CCR-15-1458
For many years, the field of cancer research has focused heavily on molecularly targeted therapy. Growth arrest-specific protein 6 (GAS6) is a high-affinity ligand that is present in AXL, a member of the TAM family.
Zhu, Chenjing, Yuquan Wei, and Xiawei Wei. "AXL receptor tyrosine kinase as a promising anti-cancer approach: functions, molecular mechanisms and clinical applications." Molecular cancer 18 (2019): 1-22.
Pubmed:
31684958
DOI:
10.1186/s12943-019-1090-3