WANG Ming-fang, LUO Zhi-fu. The current status of 18F-FLT as a proliferation tracer[J]. Int J Radiat Med Nucl Med, 2005, 29(5): 227-232.
Citation: WANG Ming-fang, LUO Zhi-fu. The current status of 18F-FLT as a proliferation tracer[J]. Int J Radiat Med Nucl Med, 2005, 29(5): 227-232.

The current status of 18F-FLT as a proliferation tracer

  • 18F-fluorodeoxyglueose (18F-FDG) is widely used to detect tumor with PET. However, 18F-FDG is not specific for tumor imaging because glucose is also utilized by other benign cells. 3'-deoxy-3'-18F-fluorothymi-dine (18F-FLT) is developed to overcome the limitations of 18F-FDG and to image cellular proliferation by PET. 18F-FLTfeatures an excellent proliferation tracerfor PET studies of tumors. The advantage of 18F-FLT is based on thymidine kinase-1 (TK 1) catalyzed phosphorylation of FLT and the intracellular accumulation of 18F-FLT is dependent on the presence of TK1, which is closely related to cellular proliferation in tumor cells undergoing DNA replication during the S phase of the cell cycle. Therefore, ISF-FLT is expected to be a feasible PET tracer for diagnosing, evaluating and monitoring the early response to therapy in oncology.
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