mProX™ Human CCR1 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- GPCR Cell Lines
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Published Data
Fig.1 In vitro transwell assays confirmed that knockdown of CCR1 receptor abolished SOX18-mediated GC metastasis.
Transwell assays conducted in a controlled laboratory setting verified that the suppression of the CCR1 receptor negated the effects of SOX18 in driving GC metastasis.
Ref: Chen, Jie, et al. "SOX18 promotes gastric cancer metastasis through transactivating MCAM and CCL7." Oncogene 39.33 (2020): 5536-5552.
Pubmed: 32616889
DOI: 10.1038/s41388-020-1378-1
Research Highlights
Xiong J, et al. "GPCR signaling contributes to immune characteristics of microenvironment and ." Science bulletin, 2023.
The Epstein-Barr virus (EBV) has been recognized as a primary cause of various cancers, yet the precise mechanism behind its interaction with the immune system during disease progression remains unclear. This study provides a comprehensive analysis of natural killer/T-cell lymphoma (NKTCL), a model disease to study EBV-related lymphomagenesis, through a variety of genomic, transcriptomic, and proteomic techniques. Results revealed a correlation between EBV gene patterns and oncogenic immune signaling, as well as distinct immune profiles within the tumor microenvironment based on single-cell transcriptome analysis. Additionally, a G-protein coupled receptor (GPCR) interactome reprogramming, likely induced by EBV interaction with transcriptional factors, was identified as a key factor in malignant progression. Targeting the chemokine receptor-1 (CCR1) showed promising results in NKTCL organoids, demonstrating its potential as a specific anti-cancer treatment against EBV. Overall, this study sheds light on the intricate relationship between EBV and cancer and provides potential therapeutic targets for EBV-related cancers.
Pubmed:
37798178
DOI:
10.1016/j.scib.2023.09.029
Chu YT, et al. "Interplay of Chemokines Receptors, Toll-like Receptors, and Host Immunological ." Biomedicines, 2023.
The researchers found that CCR5 is associated with TH1 responses, while CCR1 is linked to TH1-like responses. Additionally, CCR4 in basophils and CCR3 in eosinophils are involved in TH2 and TH9 responses, respectively. CCR10 is associated with TH22 responses, while CCR6 is involved in TH17 responses. CXCR3 is linked to THalphabeta responses, while CCR8 is associated with regulatory T cells (Treg), and CCR2 is involved in TH3 responses. These findings help identify biomarkers for immune cells and provide insights into host immunological pathways. Understanding the chemokine and Toll-like receptor system is crucial for comprehending the function of the innate immune system, as well as adaptive immune responses.
Pubmed:
37760825
DOI:
10.3390/biomedicines11092384