mProX™ Human IKBKE Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Expression of IKBKE in cell lines and silence of IKBKE using shRNA in U87-MG and LN-229.
Real-time RT-PCR and western blotting were used to confirm the effects of IKBKE prohibition in U87-MG and LN-229 cells transfected with scrambled vector or IKBKE-shRNA lentivirus. These results demonstrated how strikingly obvious the effect of suppressing IKBKE was.
Ref: Lu, Jie, et al. "IKBKE regulates cell proliferation and epithelial-mesenchymal transition of human malignant glioma via the Hippo pathway." Oncotarget 8.30 (2017): 49502.
Pubmed: 28548934
DOI: 10.18632/oncotarget.17738
Research Highlights
These results demonstrate the functional significance of IKBKE in pancreatic cancer, provide credence to the assessment of IKBKE as a therapeutic target in PDAC, and propose IKBKE inhibition as a tactic to enhance the clinical efficacy of mTOR inhibitors.
Rajurkar, Mihir, et al. "IKBKE is required during KRAS-induced pancreatic tumorigenesis." Cancer research 77.2 (2017): 320-329.
Pubmed:
28069799
DOI:
10.1158/0008-5472.CAN-15-1684
All of these findings point to the possibility of using IKBKE as a target for metastatic breast cancer treatments and uncover a novel oncogenic role of IKBKE in controlling the abundance of snails, which in turn promotes breast cancer metastasis.
Xie, Wei, et al. "IKBKE phosphorylates and stabilizes Snail to promote breast cancer invasion and metastasis." Cell Death & Differentiation 29.8 (2022): 1528-1540.
Pubmed:
35066576
DOI:
10.1038/s41418-022-00940-1