mProX™ Human MAPKAPK2 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 p38α-dependent phosphorylation of MAPKAPK2 in response to TNFα.
After being treated with 15 ng/ml TNFα, HeLa cells were subjected to immunoblotting at different periods to assess p38α and MAPKAPK2 activation. Different doses of p38α specific siRNA were applied to HeLa cells.
Ref: Fan, Li, et al. "A novel role of p38α MAPK in mitotic progression independent of its kinase activity." Cell Cycle 4.11 (2005): 1616-1624.
Pubmed: 16258274
DOI: 10.4161/cc.4.11.2125
Research Highlights
Despite the considerable challenges faced in the creation of these inhibitors, MK2 is still regarded as a promising target for the treatment of inflammation and associated illnesses, as well as for preventing tumor metastasis and enhancing tumor susceptibility to chemotherapy.
Fiore, Mario, Stefano Forli, and Fabrizio Manetti. "Targeting mitogen-activated protein kinase-activated protein kinase 2 (MAPKAPK2, MK2): medicinal chemistry efforts to lead small molecule inhibitors to clinical trials." Journal of medicinal chemistry 59.8 (2016): 3609-3634.
Pubmed:
26502061
DOI:
10.1021/acs.jmedchem.5b01457
According to this research, sophoridine presents a viable treatment option for preventing the growth of tumors in colorectal malignancies.
Wang, Rui, et al. "Sophoridine inhibits human colorectal cancer progression via targeting MAPKAPK2." Molecular Cancer Research 17.12 (2019): 2469-2479.
Pubmed:
31575657
DOI:
10.1158/1541-7786.MCR-19-0553