Auger electrons for cancer therapy – a review
Abstract Background Auger electrons (AEs) are very low energy electrons that are emitted by radionuclides that decay by electron capture (e.g. 111In, 67Ga, 99mTc, 195mPt, 125I and 123I). This energy is deposited over nanometre-micrometre distances, resulting in high linear energy transfer (LET) that...
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| Format: | Article |
| Language: | English |
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SpringerOpen
2019-10-01
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| Series: | EJNMMI Radiopharmacy and Chemistry |
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| Online Access: | http://link.springer.com/article/10.1186/s41181-019-0075-2 |
| _version_ | 1819210283072094208 |
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| author | Anthony Ku Valerie J. Facca Zhongli Cai Raymond M. Reilly |
| author_facet | Anthony Ku Valerie J. Facca Zhongli Cai Raymond M. Reilly |
| author_sort | Anthony Ku |
| collection | DOAJ |
| description | Abstract Background Auger electrons (AEs) are very low energy electrons that are emitted by radionuclides that decay by electron capture (e.g. 111In, 67Ga, 99mTc, 195mPt, 125I and 123I). This energy is deposited over nanometre-micrometre distances, resulting in high linear energy transfer (LET) that is potent for causing lethal damage in cancer cells. Thus, AE-emitting radiotherapeutic agents have great potential for treatment of cancer. In this review, we describe the radiobiological properties of AEs, their radiation dosimetry, radiolabelling methods, and preclinical and clinical studies that have been performed to investigate AEs for cancer treatment. Results AEs are most lethal to cancer cells when emitted near the cell nucleus and especially when incorporated into DNA (e.g. 125I-IUdR). AEs cause DNA damage both directly and indirectly via water radiolysis. AEs can also kill targeted cancer cells by damaging the cell membrane, and kill non-targeted cells through a cross-dose or bystander effect. The radiation dosimetry of AEs considers both organ doses and cellular doses. The Medical Internal Radiation Dose (MIRD) schema may be applied. Radiolabelling methods for complexing AE-emitters to biomolecules (antibodies and peptides) and nanoparticles include radioiodination (125I and 123I) or radiometal chelation (111In, 67Ga, 99mTc). Cancer cells exposed in vitro to AE-emitting radiotherapeutic agents exhibit decreased clonogenic survival correlated at least in part with unrepaired DNA double-strand breaks (DSBs) detected by immunofluorescence for γH2AX, and chromosomal aberrations. Preclinical studies of AE-emitting radiotherapeutic agents have shown strong tumour growth inhibition in vivo in tumour xenograft mouse models. Minimal normal tissue toxicity was found due to the restricted toxicity of AEs mostly on tumour cells targeted by the radiotherapeutic agents. Clinical studies of AEs for cancer treatment have been limited but some encouraging results were obtained in early studies using 111In-DTPA-octreotide and 125I-IUdR, in which tumour remissions were achieved in several patients at administered amounts that caused low normal tissue toxicity, as well as promising improvements in the survival of glioblastoma patients with 125I-mAb 425, with minimal normal tissue toxicity. Conclusions Proof-of-principle for AE radiotherapy of cancer has been shown preclinically, and clinically in a limited number of studies. The recent introduction of many biologically-targeted therapies for cancer creates new opportunities to design novel AE-emitting agents for cancer treatment. Pierre Auger did not conceive of the application of AEs for targeted cancer treatment, but this is a tremendously exciting future that we and many other scientists in this field envision. |
| first_indexed | 2024-12-23T06:08:43Z |
| format | Article |
| id | doaj.art-f4fb0e0c49b4487d9797184ae39712ea |
| institution | Directory Open Access Journal |
| issn | 2365-421X |
| language | English |
| last_indexed | 2024-12-23T06:08:43Z |
| publishDate | 2019-10-01 |
| publisher | SpringerOpen |
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| series | EJNMMI Radiopharmacy and Chemistry |
| spelling | doaj.art-f4fb0e0c49b4487d9797184ae39712ea2022-12-21T17:57:31ZengSpringerOpenEJNMMI Radiopharmacy and Chemistry2365-421X2019-10-014113610.1186/s41181-019-0075-2Auger electrons for cancer therapy – a reviewAnthony Ku0Valerie J. Facca1Zhongli Cai2Raymond M. Reilly3Department of Pharmaceutical Sciences, University of TorontoDepartment of Pharmaceutical Sciences, University of TorontoDepartment of Pharmaceutical Sciences, University of TorontoDepartment of Pharmaceutical Sciences, University of TorontoAbstract Background Auger electrons (AEs) are very low energy electrons that are emitted by radionuclides that decay by electron capture (e.g. 111In, 67Ga, 99mTc, 195mPt, 125I and 123I). This energy is deposited over nanometre-micrometre distances, resulting in high linear energy transfer (LET) that is potent for causing lethal damage in cancer cells. Thus, AE-emitting radiotherapeutic agents have great potential for treatment of cancer. In this review, we describe the radiobiological properties of AEs, their radiation dosimetry, radiolabelling methods, and preclinical and clinical studies that have been performed to investigate AEs for cancer treatment. Results AEs are most lethal to cancer cells when emitted near the cell nucleus and especially when incorporated into DNA (e.g. 125I-IUdR). AEs cause DNA damage both directly and indirectly via water radiolysis. AEs can also kill targeted cancer cells by damaging the cell membrane, and kill non-targeted cells through a cross-dose or bystander effect. The radiation dosimetry of AEs considers both organ doses and cellular doses. The Medical Internal Radiation Dose (MIRD) schema may be applied. Radiolabelling methods for complexing AE-emitters to biomolecules (antibodies and peptides) and nanoparticles include radioiodination (125I and 123I) or radiometal chelation (111In, 67Ga, 99mTc). Cancer cells exposed in vitro to AE-emitting radiotherapeutic agents exhibit decreased clonogenic survival correlated at least in part with unrepaired DNA double-strand breaks (DSBs) detected by immunofluorescence for γH2AX, and chromosomal aberrations. Preclinical studies of AE-emitting radiotherapeutic agents have shown strong tumour growth inhibition in vivo in tumour xenograft mouse models. Minimal normal tissue toxicity was found due to the restricted toxicity of AEs mostly on tumour cells targeted by the radiotherapeutic agents. Clinical studies of AEs for cancer treatment have been limited but some encouraging results were obtained in early studies using 111In-DTPA-octreotide and 125I-IUdR, in which tumour remissions were achieved in several patients at administered amounts that caused low normal tissue toxicity, as well as promising improvements in the survival of glioblastoma patients with 125I-mAb 425, with minimal normal tissue toxicity. Conclusions Proof-of-principle for AE radiotherapy of cancer has been shown preclinically, and clinically in a limited number of studies. The recent introduction of many biologically-targeted therapies for cancer creates new opportunities to design novel AE-emitting agents for cancer treatment. Pierre Auger did not conceive of the application of AEs for targeted cancer treatment, but this is a tremendously exciting future that we and many other scientists in this field envision.http://link.springer.com/article/10.1186/s41181-019-0075-2Auger electrons111InMonoclonal antibodiesNanoparticlesPeptidesDosimetry |
| spellingShingle | Anthony Ku Valerie J. Facca Zhongli Cai Raymond M. Reilly Auger electrons for cancer therapy – a review EJNMMI Radiopharmacy and Chemistry Auger electrons 111In Monoclonal antibodies Nanoparticles Peptides Dosimetry |
| title | Auger electrons for cancer therapy – a review |
| title_full | Auger electrons for cancer therapy – a review |
| title_fullStr | Auger electrons for cancer therapy – a review |
| title_full_unstemmed | Auger electrons for cancer therapy – a review |
| title_short | Auger electrons for cancer therapy – a review |
| title_sort | auger electrons for cancer therapy a review |
| topic | Auger electrons 111In Monoclonal antibodies Nanoparticles Peptides Dosimetry |
| url | http://link.springer.com/article/10.1186/s41181-019-0075-2 |
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