mProX™ Human MARK2 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 MARK2 regulates MT growth dynamics and orientation downstream of Rac1.
Lysates from U2-OS cells transfected with non-targeting siRNA pool (lane 4), MARK2-shRNA (lane 2), control shRNA (lane 1), MARK2-shRNA (lane 2), and MARK2-shRNA and shRNA-resistant GFP-MARK2 (lane 3).
Ref: Nishimura, Yukako, et al. "Automated screening of microtubule growth dynamics identifies MARK2 as a regulator of leading edge microtubules downstream of Rac1 in migrating cells." PloS one 7.7 (2012): e41413.
Pubmed: 22848487
DOI: 10.1371/journal.pone.0041413
Research Highlights
The information showed that MARK2/4 promotes metabolic reprogramming in NSCLC cells, which is how it causes cancer. As a result, MARK2/4 may be a viable target for lung cancer treatment.
Natarajan, Sathan Raj, Lavanya Ponnusamy, and Ravi Manoharan. "MARK2/4 promotes Warburg effect and cell growth in non-small cell lung carcinoma through the AMPKα1/mTOR/HIF-1α signaling pathway." Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1869.7 (2022): 119242.
Pubmed:
35192892
DOI:
10.1016/j.bbamcr.2022.119242
In unperturbed mitosis and in response to antitubulin chemotherapy, MARK2 is phosphorylated by CDK1. MARK2 requires phosphorylation to control the course of mitosis and the cytotoxicity of paclitaxel in PDAC cells.
Zeng, Yongji, et al. "MARK2 regulates chemotherapeutic responses through class IIa HDAC-YAP axis in pancreatic cancer." Oncogene 41.31 (2022): 3859-3875.
Pubmed:
35780183
DOI:
10.1038/s41388-022-02399-3