mProX™ Human ADGRE5 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- GPCR Cell Lines
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Published Data
Fig.1 HT1080 cells stably expressing genetically engineered CD97 protein
The expression of CD97 and EMR2 molecules in HT1080 stably transfected cells was confirmed by flow cytometry and western blotting analyses using appropriate mAbs as indicated.
Ref: Tjong, W. Y., & Lin, H. H. The RGD motif is involved in CD97/ADGRE5-promoted cell adhesion and viability of HT1080 cells. Scientific reports. 2019, 9(1), 1-12.
Pubmed: 30728423
DOI: 10.1038/s41598-018-38045-w
Research Highlights
Adhesion G protein-coupled receptors (aGPCRs) control cellular activities that are directly related to the biology of tumor cells. Individual human aGPCRs were discovered to be implicated in carcinogenesis not long after they were originally characterized.
Aust, G., et al. To Detach, Migrate, Adhere, and Metastasize: CD97/ADGRE5 in Cancer. Cells. 2022, 11(9), 1538.
Pubmed:
35563846
DOI:
10.3390/cells11091538
EMR2 demonstrated broad G protein-coupling in a yeast-based experiment in which heterologous GPCRs are coupled to chimeric G proteins, whereas CD97 coupled more selectively to Gα12, Gα13, Gα14, and Gαz chimeras.
Bhudia, N., et al. G protein-coupling of adhesion GPCRs ADGRE2/EMR2 and ADGRE5/CD97, and activation of G protein signalling by an anti-EMR2 antibody. Scientific reports. 2020, 10(1), 1-13.
Pubmed:
31969668
DOI:
10.1038/s41598-020-57989-6
In non-CNS malignancies, the surface receptor CD97/ADRGE5 is linked to the control of invasion and metastasis. Although CD97 expression is positively correlated with a bad prognosis for GBM patients, its function in this tumor is not fully understood.
Eichberg, D. G., et al. Genetic manipulation of adhesion GPCR CD97/ADGRE5 modulates invasion in patient-derived glioma stem cells. Journal of neuro-oncology. 2021, 153(3), 383-391.
Pubmed:
34028660
DOI:
10.1007/s11060-021-03778-8