SPECT imaging and radionuclide therapy of glioma using 131I labeled Buthus martensii Karsch chlorotoxin
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Published on: December 28, 2017
Wenli Qiao1,2, Lingzhou Zhao2, Shan Wu2
1Department of Nuclear Medicine, Shanghai General Hospital of Nanjing Medical University, Shanghai, 200080, China.
Abstract:
Gliomas, the most prevalent type of brain tumor in adults, are associated with high rates of morbidity and mortality. Recent studies on 131I labeled scorpion toxins suggest they can be developed as tumor-specific agents for glioma diagnosis and treatment. This study investigated the potential of 131I labeled Buthus martensii Karsch chlorotoxin (131I-BmK CT) as a new approach for targeted imaging and therapy of glioma. The results showed that 131I can be successfully linked to BmK CT with satisfactory radiochemical purity and stability and that 131I-BmK CT markedly inhibited glioma cell growth in a dose and time dependent manner, with significant accumulation in glioma cells in vitro. Persistent intratumoral radioiodine retention and specific accumulation of 131I-BmK CT were observed in C6 glioma tumor, which was clearly visualized by SPECT imaging. Both intratumoral and intravenous injections of 131I-BmK CT could result in significant tumor inhibition efficacy and prolonging the lifetime of tumor-bearing mice. Based on these promising results, it is concluded that 131I-BmK CT has the potential to be explored as a novel tool for SPECT imaging and radionuclide therapy of glioma.
Insights
Iodine-131 labeled Buthus martensii Karsch chlorotoxin (131I-BmK CT) shows promise for glioma diagnosis and therapy. This targeted agent effectively inhibits glioma growth and aids in tumor visualization via SPECT imaging.
Area of Science:
- Oncology
- Nuclear Medicine
- Biochemistry
Background:
- Gliomas are the most common adult brain tumors, linked to significant morbidity and mortality.
- Scorpion toxins labeled with Iodine-131 (131I) are emerging as potential tumor-specific agents for glioma management.
- Developing targeted diagnostic and therapeutic agents for gliomas remains a critical unmet need.
Purpose of the Study:
- To investigate the potential of 131I-labeled Buthus martensii Karsch chlorotoxin (131I-BmK CT) for targeted glioma imaging and therapy.
- To evaluate the efficacy and safety of 131I-BmK CT in preclinical glioma models.
Main Methods:
- Radiolabeling of Buthus martensii Karsch chlorotoxin with 131I.
- In vitro assessment of 131I-BmK CT's cytotoxicity and cellular uptake in glioma cells.
- In vivo evaluation of 131I-BmK CT's tumor accumulation, imaging characteristics (SPECT), and therapeutic efficacy in a C6 glioma mouse model.
Main Results:
- Successful radiolabeling of BmK CT with 131I, achieving high radiochemical purity and stability.
- 131I-BmK CT demonstrated dose- and time-dependent inhibition of glioma cell growth and significant in vitro accumulation in glioma cells.
- Persistent intratumoral radioiodine retention and specific accumulation of 131I-BmK CT were observed in vivo, enabling clear SPECT visualization of C6 gliomas.
- Both intratumoral and intravenous administration of 131I-BmK CT significantly inhibited tumor growth and prolonged survival in tumor-bearing mice.
Conclusions:
- 131I-BmK CT is a promising radiolabeled toxin with potential for targeted glioma diagnosis and radionuclide therapy.
- The study supports further exploration of 131I-BmK CT as a novel theranostic agent for gliomas.
- 131I-BmK CT offers a potential new avenue for improving outcomes in patients with malignant gliomas.
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