Development of Stem-Cell-Mobilizing Agents Targeting CXCR4 Receptor for Peripheral Blood Stem Cell Transplantation and Beyond.
Chien-Huang WuJen-Shin SongHsuan-Hao KuanSzu-Huei WuMing-Chen ChouJiing-Jyh JanLun Kelvin TsouYi-Yu KeChiung-Tong ChenKai-Chia YehSing-Yi WangTeng-Kuang YehChen-Tso TsengChen-Lung HuangMine-Hsine WuPo-Chu KuoChia-Jui LeeKak-Shan ShiaPublished in: Journal of medicinal chemistry (2018)
The function of the CXCR4/CXCL12 axis accounts for many disease indications, including tissue/nerve regeneration, cancer metastasis, and inflammation. Blocking CXCR4 signaling with its antagonists may lead to moving out CXCR4+ cell types from bone marrow to peripheral circulation. We have discovered a novel series of pyrimidine-based CXCR4 antagonists, a representative (i.e., 16) of which was tolerated at a higher dose and showed better HSC-mobilizing ability at the maximal response dose relative to the approved drug 1 (AMD3100), and thus considered a potential drug candidate for PBSCT indication. Docking compound 16 into the X-ray crystal structure of CXCR4 receptor revealed that it adopted a spider-like conformation striding over both major and minor subpockets. This putative binding mode provides a new insight into CXCR4 receptor-ligand interactions for further structural modifications.
Keyphrases
- stem cells
- stem cell transplantation
- cell migration
- bone marrow
- peripheral blood
- single cell
- oxidative stress
- mesenchymal stem cells
- binding protein
- emergency department
- high resolution
- mass spectrometry
- cell therapy
- papillary thyroid
- molecular dynamics simulations
- low dose
- body composition
- computed tomography
- blood pressure
- magnetic resonance
- resistance training
- climate change
- young adults