mProX™ Human DYRK1B Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 High throughput screening with the kinome siRNA library for kinases essential for cell viability of TNBC cells.
According to these findings, DYRK1B exhibited the greatest selectivity for cell viability between normal and TNBC cells when compared to the varying outcomes of other candidate gene knockdowns. Three distinct siRNAs were used to effectively silence DYRK1B in order to remove the off-target effects of siRNA.
Ref: Chang, Chia-Che, et al. "Kinome-wide siRNA screening identifies DYRK1B as a potential therapeutic target for triple-negative breast cancer cells." Cancers 13.22 (2021): 5779.
Pubmed: 34830933
DOI: 10.3390/cancers13225779
Research Highlights
When combined, the study's results offer fresh perspectives on the hitherto unknown function of DYRK1B in mitochondrial bioenergetics and the development of ventricular hypertrophy and heart failure. As a result, these discoveries might provide patients with heart failure new treatment alternatives.
Zhuang, Lingfang, et al. "DYRK1B-STAT3 drives cardiac hypertrophy and heart failure by impairing mitochondrial bioenergetics." Circulation 145.11 (2022): 829-846.
Pubmed:
35235343
DOI:
10.1161/CIRCULATIONAHA.121.055727
These results identified Dyrk1b as a therapeutic target for NASH and insulin resistance in the liver and shed light on the mechanisms underlying hepatic lipogenesis and hepatic insulin resistance caused by Dyrk1b.
Bhat, Neha, et al. "Dyrk1b promotes hepatic lipogenesis by bypassing canonical insulin signaling and directly activating mTORC2 in mice." The Journal of Clinical Investigation 132.3 (2022).
Pubmed:
34855620
DOI:
10.1172/JCI153724