mProX™ Human DDR1 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 DDR1 and IGF-IR expression in a panel of cultured cells.
Using polyclonal antibodies against the C-terminus of DDR1 and the C-terminus of IGF-IR, as indicated, a panel of cell lines, including human breast cancer (MCF-7, T47D, ZR-75, MDA-MB-157, MDA-MB-231, and BT-474), human hepatoblastoma (HepG2), and mouse embryo fibroblasts, were subjected to western immunoblot analysis for DDR1 and IGF-IR expression.
Ref: Malaguarnera, Roberta, et al. "Novel cross-talk between IGF-IR and DDR1 regulates IGF-IR trafficking, signaling and biological responses." Oncotarget 6.18 (2015): 16084.
Pubmed: 25840417
DOI: 10.18632/oncotarget.3177
Research Highlights
A collagen-activated receptor tyrosine kinase, discoidin domain receptor 1 (DDR1) is a desirable anti-fibrotic target. Its expression is mostly restricted to epithelial cells found in the skin, kidney, liver, and lungs, among other organs.
Moll, Solange, et al. "DDR1 role in fibrosis and its pharmacological targeting." Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1866.11 (2019): 118474.
Pubmed:
30954571
DOI:
10.1016/j.bbamcr.2019.04.004
These results pinpoint a mechanism of immune exclusion and propose an immunotherapeutic strategy to enhance immune accessibility by reorganizing the extracellular matrix of the tumor.
Sun, Xiujie, et al. "Tumour DDR1 promotes collagen fibre alignment to instigate immune exclusion." Nature 599.7886 (2021): 673-678.
Pubmed:
34732895
DOI:
10.1038/s41586-021-04057-2