mProX™ Human AKT1 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Differential sensitivity of human cancer cells to different classes of AKT inhibitors.
AKT inhibitors' impact on AKT and AKT protein substrate phosphorylation. The stated doses of MK2206 and GSK690693 (top) or GDC0068 (bottom) were applied to EBC1 cells for a duration of 24 hours. Lysed treated cells were subjected to immunoblotting using the designated antibodies. Using image densitometry, the phosphorylation of GSK3β, BAD, and PRAS40 was measured (middle).
Ref: Vivanco, Igor, et al. "A kinase-independent function of AKT promotes cancer cell survival." Elife 3 (2014): e03751.
Pubmed: 25551293
DOI: 10.7554/eLife.03751
Research Highlights
It is widely accepted that Akt isoforms promote cancer by increasing cell proliferation and suppressing apoptosis in cancer cells and the tissues around tumors. Interestingly, research also shows that the Akt pathway is critical for tumor perfusion and metastasis, as well as for maintaining the integrity of the endothelium barrier and preventing aberrant vascular permeability.
Alwhaibi, Abdulrahman, et al. "The unconventional role of Akt1 in the advanced cancers and in diabetes-promoted carcinogenesis." Pharmacological research 145 (2019): 104270.
Pubmed:
31078742
DOI:
10.1016/j.phrs.2019.104270
The results show that resveratrol mitigates the unanticipated potential for metastasis brought on by anti-AKT therapy, indicating that resveratrol supplementation to an anti-AKT treatment regimen may offer additional assistance in preventing EMT.
Li, Chia-Wei, et al. "AKT1 inhibits epithelial-to-mesenchymal transition in breast cancer through phosphorylation-dependent Twist1 degradation." Cancer research 76.6 (2016): 1451-1462.
Pubmed:
26759241
DOI:
10.1158/0008-5472.CAN-15-1941