4.5 Article

Radiation-guided P-selectin antibody targeted to lung cancer

期刊

ANNALS OF BIOMEDICAL ENGINEERING
卷 36, 期 5, 页码 821-830

出版社

SPRINGER
DOI: 10.1007/s10439-008-9444-9

关键词

P-selectin; radiation; lung cancer; optical imaging; nuclear imaging

资金

  1. Intramural NIH HHS [Z01 SC006353-24] Funding Source: Medline
  2. NCI NIH HHS [P30-CA68485, R01-CA1256757, R21 CA128456, R01 CA112385, R21-CA128456, R01-CA112385, P30 CA068485] Funding Source: Medline

向作者/读者索取更多资源

Purpose: P-selectin expression is significantly increased in tumor microvasculature following exposure to ionizing radiation. The purpose of this study was to image radiation-induced P-selectin expression in vivo using optical imaging and gamma camera imaging in a heterotopic lung cancer model by using ScFv antibodies to P-selectin. Procedures: In vitro studies using endothelial cells were done using 3 Gy radiation and selected ScFv antibodies to P-selectin. In vivo studies were performed using Lewis lung carcinoma cells subcutaneously injected into the hind limbs of nude mice. Mice were treated with 6 Gy radiation and sham radiation 10 days post-inoculation. P-selectin expression was assessed with near-infrared imaging using Cy7 labeled antibody, and gamma camera imaging using In-111-DTPA labeled antibody. Results: In vitro studies showed antibody binding to P-selectin in radiation treated endothelial cells. In vivo optical imaging and gamma camera imaging studies showed significant tumor-specific binding to P-selectin in irradiated tumors compared to unirradiated tumors. Conclusions: Optical imaging and gamma camera imaging are effective methods for visualizing in vivo targeting of radiation-induced P-selectin in lung tumors. This study suggests that fluorescent-labeled and radiolabeled ScFv antibodies can be used to target radiation-induced P-selectin for the tumor-specific delivery of therapeutic drugs and radionuclides in vivo.

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