mProX™ Human DYRK4 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 DYRK gene NB tumor mRNA expression and prognostic significance.
The DYRK gene family's mRNA expression was examined in SEQC-498, the most publicly available genome-wide RNA sequencing dataset on human NB tumors. Bar chart showing the tumor mRNA expression of the DYRK gene in the SEQC-498 patient group.
Ref: Uhl, Katie L., et al. "Harmine, a dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor induces caspase-mediated apoptosis in neuroblastoma." Cancer cell international 18.1 (2018): 1-14.
Pubmed: 29977157
DOI: 10.1186/s12935-018-0574-3
Research Highlights
This finding provides insights into a novel aspect of the molecular pathobiology of luminal B cancers and suggests new avenues for the treatment of more aggressive breast tumors that overexpress this fusion.
Liu, Chia-Chia, et al. "A novel neoplastic fusion transcript, RAD51AP1-DYRK4, confers sensitivity to the MEK inhibitor trametinib in aggressive breast cancers." Clinical Cancer Research 27.3 (2021): 785-798.
Pubmed:
33172895
DOI:
10.1158/1078-0432.CCR-20-2769
The study found a link between peripheral blood DYRK4 hypomethylation and LC, indicating that blood-based DNA methylation may be a viable novel biomarker for LC detection.
Qiao, Rong, et al. "Hypomethylation of DYRK4 in peripheral blood is associated with increased lung cancer risk." Molecular Carcinogenesis (2023).
Pubmed:
37530470
DOI:
10.1002/mc.23612