Chemokine receptor 4 targeted protein MRI contrast agent for early detection of liver metastases.
Shanshan TanHua YangShenghui XueJingjuan QiaoMani SalarianKhan HekmatyarYuguang MengRao MukkavilliFan PuOluwatosin Y OdubadeWayne HarrisYan HaiMelinda L YushakVanessa M Morales-TiradoPardeep K MittalPhillip Zhe SunDavid LawsonHans E GrossniklausJenny J YangPublished in: Science advances (2020)
Liver metastases often progress from primary cancers including uveal melanoma (UM), breast, and colon cancer. Molecular biomarker imaging is a new non-invasive approach for detecting early stage tumors. Here, we report the elevated expression of chemokine receptor 4 (CXCR4) in liver metastases in UM patients and metastatic UM mouse models, and development of a CXCR4-targeted MRI contrast agent, ProCA32.CXCR4, for sensitive MRI detection of UM liver metastases. ProCA32.CXCR4 exhibits high relaxivities (r 1 = 30.9 mM-1 s-1, r 2 = 43.2 mM-1 s-1, 1.5 T; r 1 = 23.5 mM-1 s-1, r 2 = 98.6 mM-1 s-1, 7.0 T), strong CXCR4 binding (K d = 1.10 ± 0.18 μM), CXCR4 molecular imaging capability in metastatic and intrahepatic xenotransplantation UM mouse models. ProCA32.CXCR4 enables detecting UM liver metastases as small as 0.1 mm3. Further development of the CXCR4-targeted imaging agent should have strong translation potential for early detection, surveillance, and treatment stratification of liver metastases patients.
Keyphrases
- liver metastases
- cell migration
- end stage renal disease
- contrast enhanced
- early stage
- magnetic resonance imaging
- newly diagnosed
- mouse model
- ejection fraction
- chronic kidney disease
- small cell lung cancer
- high resolution
- squamous cell carcinoma
- magnetic resonance
- peritoneal dialysis
- binding protein
- prognostic factors
- computed tomography
- cancer therapy
- radiation therapy
- diffusion weighted imaging
- risk assessment
- climate change
- transcription factor
- single molecule
- amino acid