Small molecule activator of Nm23/NDPK as an inhibitor of metastasis.
Jae-Jin LeeHwang Suk KimJi-Sun LeeJimin ParkSang Chul ShinSoonwha SongEunsun LeeJung-Eun ChoiJi-Wan SuhHongsoo LeeEunice EunKyeong KimEun Kyoung SeoDong Hae ShinHo-Young LeeHee-Yoon LeeKong-Joo LeePublished in: Scientific reports (2018)
Nm23-H1/NDPK-A is a tumor metastasis suppressor having NDP kinase (NDPK) activity. Nm23-H1 is positively associated with prolonged disease-free survival and good prognosis of cancer patients. Approaches to increasing the cellular levels of Nm23-H1 therefore have significance in the therapy of metastatic cancers. We found a small molecule, (±)-trans-3-(3,4-dimethoxyphenyl)-4-[(E)-3,4-dimethoxystyryl]cyclohex-1-ene, that activates Nm23, hereafter called NMac1. NMac1 directly binds to Nm23-H1 and increases its NDPK activity. Employing various NMac1 derivatives and hydrogen/deuterium mass spectrometry (HDX-MS), we identified the pharmacophore and mode of action of NMac1. We found that NMac1 binds to the C-terminal of Nm23-H1 and induces the NDPK activation through its allosteric conformational changes. NMac1-treated MDA-MB-231 breast cancer cells showed dramatic changes in morphology and actin-cytoskeletal organization following inhibition of Rac1 activation. NMac1 also suppressed invasion and migration in vitro, and metastasis in vivo, in a breast cancer mouse model. NMac1 as an activator of NDPK has potential as an anti-metastatic agent.
Keyphrases
- small molecule
- photodynamic therapy
- mass spectrometry
- breast cancer cells
- free survival
- squamous cell carcinoma
- mouse model
- small cell lung cancer
- light emitting
- protein protein
- molecular dynamics
- risk assessment
- cell migration
- multiple sclerosis
- single molecule
- ms ms
- nuclear factor
- bone marrow
- molecular docking
- gas chromatography
- cell proliferation
- young adults
- toll like receptor
- capillary electrophoresis
- visible light