mProX™ Human ADRB2 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- GPCR Cell Lines
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Published Data
Fig.1 Effect of β-adrenergic signalling on the proliferation of GC cells in vitro
Silencing ADRB2 gene expression and subsequent assessment using CCK8 assay to confirm the impact of diverse ADRB agonists on gastric cancer cell proliferation.
Ref: Zhang, X., et al. "Chronic stress promotes gastric cancer progression and metastasis: an essential role for ADRB2. Cell Death Dis. 2019; 10 (11): 788."
Pubmed: 31624248
DOI: 10.1038/s41419-019-2030-2
Research Highlights
Mhatre I, et al. "Functional mutation, splice, distribution, and divergence analysis of impactful ." Scientific reports, 2023.
In this study, the researchers aimed to identify key genes associated with cardiovascular disease (CVD), particularly heart failure (HF), and understand their role in the disease. A cohort of 35 consented patients was sequenced to generate whole genome sequence (WGS) data. Functional mutation, splice, variant distribution, and divergence analysis were then performed to investigate the relationship between each type of mutation and its impact. The results showed that FLNA, CST3, LGALS3, and HBA1 were linked to enrichment pathways and genes like ACE, MME, LGALS3, NR3C2, PIK3C2A, CALD1, TEK, and TRPV1 were potentially significant. Furthermore, intron, 5' Flank, 3' UTR, and 3' Flank mutations were found to be the most common, while missense mutations had a higher functional impact. Based on their divergence analysis, the researchers concluded that HBA1, FADD, NPPC, ADRB2, ADBR1, MYH6, and PLN were consequential genes in CVD and HF.
Pubmed:
37798313
DOI:
10.1038/s41598-023-44127-1
Wang K, et al. "Human engineered cardiac tissue model of hypertrophic cardiomyopathy ." Frontiers in bioengineering and biotechnology, 2023.
The development of patient-specific induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) provides a unique opportunity to study the relationship between genotype and phenotype in hypertrophic cardiomyopathy (HCM), a commonly inherited cardiac disease.
Pubmed:
37771571
DOI:
10.3389/fbioe.2023.1227184