Re-assessing gallium-67 as a therapeutic radionuclide

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• 作者：Muhamad F. bin Othman^a ; Nabil R. Mitry^a ; Valerie J. Lewington^b ; Philip J. Blower^a ; Samantha Y.A. Terry^a ; ^{samantha.terry@kcl.ac.uk}
• 关键词：Gallium-67 ; Radionuclide therapy ; Auger electrons ; Clonogenic assay
• 刊名：Nuclear Medicine and Biology
• 出版年：2017
• 出版时间：March 2017
• 年：2017
• 卷：46
• 期：Complete
• 页码：12-18
• 全文大小：683 K
• 卷排序：46

文摘

Despite its desirable half-life and low energy Auger electrons that travel further than for other radionuclides, 67Ga has been neglected as a therapeutic radionuclide. Here, 67Ga is compared with Auger electron emitter 111In as a potential therapeutic radionuclide.MethodsPlasmid pBR322 studies allowed direct comparison between 67Ga and 111In (1 MBq) in causing DNA damage, including the effect of chelators (EDTA and DTPA) and the effects of a free radical scavenger (DMSO). The cytotoxicity of internalized (by means of delivery in the form of oxine complexes) and non-internalized 67Ga and 111In was measured in DU145 prostate cancer cells after a one-hour incubation using cell viability (trypan blue) and clonogenic studies. MDA-MB-231 and HCC1954 cells were also used.ResultsPlasmid DNA damage was caused by 67Ga and was comparable to that caused by 111In; it was reduced in the presence of EDTA, DTPA and DMSO. The A50 values (internalized activity of oxine complexes per cell required to kill 50% of cells) as determined by trypan blue staining was 1.0 Bq/cell for both 67Ga and 111In; the A50 values determined by clonogenic assay were 0.7 Bq/cell and 0.3 Bq/cell for 111In and 67Ga respectively. At the concentrations required to achieve these uptake levels, non-internalized 67Ga and 111In caused no cellular toxicity. Qualitatively similar results were found for MDA-MB-231 and HCC1954 cells.Conclusion67Ga causes as much damage as 111In to plasmid DNA in solution and shows similar toxicity as 111In at equivalent internalized activity per cell. 67Ga therefore deserves further evaluation for radionuclide therapy.Advances in knowledge and implications for patient careThe data presented here is at the basic level of science. If future in vivo and clinical studies are successful, 67Ga could become a useful radionuclide with little healthy tissue toxicity in the arsenal of weapons for treating cancer.