The Journey of DDR1 and DDR2 Kinase Inhibitors as Rising Stars in the Fight Against Cancer.
Ahmed ElkamhawyQili LuHossam NadaJiyu WooGuofeng QuanKyeong LeePublished in: International journal of molecular sciences (2021)
Discoidin domain receptor (DDR) is a collagen-activated receptor tyrosine kinase that plays critical roles in regulating essential cellular processes such as morphogenesis, differentiation, proliferation, adhesion, migration, invasion, and matrix remodeling. As a result, DDR dysregulation has been attributed to a variety of human cancer disorders, for instance, non-small-cell lung carcinoma (NSCLC), ovarian cancer, glioblastoma, and breast cancer, in addition to some inflammatory and neurodegenerative disorders. Since the target identification in the early 1990s to date, a lot of efforts have been devoted to the development of DDR inhibitors. From a medicinal chemistry perspective, we attempted to reveal the progress in the development of the most promising DDR1 and DDR2 small molecule inhibitors covering their design approaches, structure-activity relationship (SAR), biological activity, and selectivity.
Keyphrases
- tyrosine kinase
- small molecule
- papillary thyroid
- small cell lung cancer
- epidermal growth factor receptor
- single cell
- endothelial cells
- structure activity relationship
- stem cells
- signaling pathway
- staphylococcus aureus
- mesenchymal stem cells
- quality improvement
- childhood cancer
- genome wide
- escherichia coli
- binding protein
- lymph node metastasis
- protein protein