A through interactions with fibronectin, a glycoprotein of extracellular matrix (ECM) protein and vascular cell adhesion molecule-1 (VCAM-1) protein expressed on bone marrow (BM) stromal cells. B. Structure of CB-TE1A1P-LLP2A. doi:10.1371/journal.pone.0055841.gmyeloma cells with stromal cells via a4b1-integrin/VCAM-1 produces osteoclastogenic 
activity, suggesting that the presence of stromal cells provide a microenvironment for exclusive colonization of myeloma cells in the BM [12]. VLA-4 also plays an important role in the development of chemotherapy resistance. Noborio-Hatano et al. reported that high expression of VLA-4 on the cell surface leads to acquisition of chemotherapy resistance in MM [8]. VLA-4 mediated adhesion and an up-regulated VLA-4 axis is also observed in MM patients who demonstrate chemotherapeutic resistance [17?9]. VLA-4, therefore, is a useful marker of tumor cell trafficking, osteoclast stimulation and drug resistance in MM. Biomedical imaging techniques such as FDG/PET, skeletal survey, bone scintigraphy and MRI are routinely used for staging and post-treatment follow up in MM patients [20]. More importantly, imaging of the skeleton with the aim of detecting lytic bone lesions is needed to discriminate MM from its precursor states such as smoldering MM (sMM) and monoclonal gammopathy of undetermined significance (MGUS) [21]. Radiographic skeletal MedChemExpress KS 176 survey can detect osteolytic lesions only after 30 ?0 cortical bone destruction, limiting its sensitivity for imaging early stage myeloma bone lesions. MRI and FDG-PET/CT are comparatively better at detecting bone marrow plasma cell Lixisenatide web infiltration than conventional radiographs[22]. However, MRI has limitations such as prolonged acquisition time (45?0 min), limiting patient factors such as claustrophobia or metal devices in the body, and particularly, the limited field of view of MRI is not reliable for investigating bones such as skull, clavicle or ribs, and causes frequent understaging. FDG is a marker of cell metabolism that has limited sensitivity (61 ) for intramedullary lesions in MM [23]. Additionally, FDG/PET scan is not recommended within two months following therapy due to high likelihood of healing related (flare phenomenon) false positives. Currently, there are no specific MM imaging agents used clinically. VLA-4 targeted novel molecular imaging of MM has the potential to improve early-stage diagnosis and the management of patients receiving compounds that affect the tumor cells as well as the microenvironment. Here, we evaluated a VLA-4 targeted PET radiopharmaceutical, 64Cu-CB-TE1A1P-LLP2A, (Figure 1B) for PET imaging of VLA-4 positive murine myeloma 5TGM1 MM tumors. For the proof-of-principle imaging studies, we used the 5TGM1 mouse model of bone marrow disseminated mouse MM. The 5TGM1into-KaLwRij model originates from spontaneously developed MM in aged C57BL/KalwRij mice and has since been propagated by intravenous injection of BM cells from MM bearing mice, into young naive syngeneic recipients [24]. CellPET iImaging of Multiple Myelomauptake and binding assays performed with 5TGM1 cells demonstrated receptor 
specific binding of the imaging probe. Tissue biodistribution and small animal PET/CT imaging studies demonstrated highly sensitive and specific uptake of the imaging probe by the subcutaneous (s.c.) and intra-peritoneal (i.p.) 5TGM1 tumors, and suspected tumor cells and associated inflammatory cells in the BM. Additionally, the imaging probe demonst.A through interactions with fibronectin, a glycoprotein of extracellular matrix (ECM) protein and vascular cell adhesion molecule-1 (VCAM-1) protein expressed on bone marrow (BM) stromal cells. B. Structure of CB-TE1A1P-LLP2A. doi:10.1371/journal.pone.0055841.gmyeloma cells with stromal cells via a4b1-integrin/VCAM-1 produces osteoclastogenic activity, suggesting that the presence of stromal cells provide a microenvironment for exclusive colonization of myeloma cells in the BM [12]. VLA-4 also plays an important role in the development of chemotherapy resistance. Noborio-Hatano et al. reported that high expression of VLA-4 on the cell surface leads to acquisition of chemotherapy resistance in MM [8]. VLA-4 mediated adhesion and an up-regulated VLA-4 axis is also observed in MM patients who demonstrate chemotherapeutic resistance [17?9]. VLA-4, therefore, is a useful marker of tumor cell trafficking, osteoclast stimulation and drug resistance in MM. Biomedical imaging techniques such as FDG/PET, skeletal survey, bone scintigraphy and MRI are routinely used for staging and post-treatment follow up in MM patients [20]. More importantly, imaging of the skeleton with the aim of detecting lytic bone lesions is needed to discriminate MM from its precursor states such as smoldering MM (sMM) and monoclonal gammopathy of undetermined significance (MGUS) [21]. Radiographic skeletal survey can detect osteolytic lesions only after 30 ?0 cortical bone destruction, limiting its sensitivity for imaging early stage myeloma bone lesions. MRI and FDG-PET/CT are comparatively better at detecting bone marrow plasma cell infiltration than conventional radiographs[22]. However, MRI has limitations such as prolonged acquisition time (45?0 min), limiting patient factors such as claustrophobia or metal devices in the body, and particularly, the limited field of view of MRI is not reliable for investigating bones such as skull, clavicle or ribs, and causes frequent understaging. FDG is a marker of cell metabolism that has limited sensitivity (61 ) for intramedullary lesions in MM [23]. Additionally, FDG/PET scan is not recommended within two months following therapy due to high likelihood of healing related (flare phenomenon) false positives. Currently, there are no specific MM imaging agents used clinically. VLA-4 targeted novel molecular imaging of MM has the potential to improve early-stage diagnosis and the management of patients receiving compounds that affect the tumor cells as well as the microenvironment. Here, we evaluated a VLA-4 targeted PET radiopharmaceutical, 64Cu-CB-TE1A1P-LLP2A, (Figure 1B) for PET imaging of VLA-4 positive murine myeloma 5TGM1 MM tumors. For the proof-of-principle imaging studies, we used the 5TGM1 mouse model of bone marrow disseminated mouse MM. The 5TGM1into-KaLwRij model originates from spontaneously developed MM in aged C57BL/KalwRij mice and has since been propagated by intravenous injection of BM cells from MM bearing mice, into young naive syngeneic recipients [24]. CellPET iImaging of Multiple Myelomauptake and binding assays performed with 5TGM1 cells demonstrated receptor specific binding of the imaging probe. Tissue biodistribution and small animal PET/CT imaging studies demonstrated highly sensitive and specific uptake of the imaging probe by the subcutaneous (s.c.) and intra-peritoneal (i.p.) 5TGM1 tumors, and suspected tumor cells and associated inflammatory cells in the BM. Additionally, the imaging probe demonst.