Validation of 64Cu-ATSM damaging DNA via high-LET Auger electron emission

J Radiat Res. 2015 Sep;56(5):784-91. doi: 10.1093/jrr/rrv042. Epub 2015 Aug 6.

Abstract

Radioactive copper (II) (diacetyl-bis N4-methylthiosemicarbazone) (Cu-ATSM) isotopes were originally developed for the imaging of hypoxia in tumors. Because the decay of a (64)Cu atom is emitting not only positrons but also Auger electrons, this radionuclide has great potential as a theranostic agent. However, the success of (64)Cu-ATSM internal radiation therapy would depend on the contribution of Auger electrons to tumor cell killing. Therefore, we designed a cell culture system to define the contributions to cell death from Auger electrons to support or refute our hypothesis that the majority of cell death from (64)Cu-ATSM is a result of high-LET Auger electrons and not positrons or other low-LET radiation. Chinese hamster ovary (CHO) wild type and DNA repair-deficient xrs5 cells were exposed to (64)Cu-ATSM during hypoxic conditions. Surviving fractions were compared with those surviving gamma-radiation, low-LET hadron radiation, and high-LET heavy ion exposure. The ratio of the D(10) values (doses required to achieve 10% cell survival) between CHO wild type and xrs5 cells suggested that (64)Cu-ATSM toxicity is similar to that of high-LET Carbon ion radiation (70 keV/μm). γH2AX foci assays confirmed DNA double-strand breaks and cluster damage by high-LET Auger electrons from (64)Cu decay, and complex types of chromosomal aberrations typical of high-LET radiation were observed after (64)Cu-ATSM exposure. The majority of cell death was caused by high-LET radiation. This work provides strong evidence that (64)Cu-ATSM damages DNA via high-LET Auger electrons, supporting further study and consideration of (64)Cu-ATSM as a cancer treatment modality for hypoxic tumors.

Keywords: 64Cu-ATSM; CHO; DNA double strand break; auger electron; high LET.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • Carbon
  • Cell Hypoxia
  • Cell Survival
  • Chromosome Aberrations
  • Coordination Complexes
  • Copper / chemistry
  • Copper Radioisotopes / chemistry*
  • Cricetinae
  • Cricetulus
  • DNA Breaks, Double-Stranded
  • DNA Damage*
  • DNA Repair
  • Electrons
  • Histones / metabolism
  • Organometallic Compounds / chemistry*
  • Radiopharmaceuticals / chemistry
  • Thiosemicarbazones / chemistry*

Substances

  • Coordination Complexes
  • Copper Radioisotopes
  • Histones
  • Organometallic Compounds
  • Radiopharmaceuticals
  • Thiosemicarbazones
  • copper (II) diacetyl-di(N(4)-methylthiosemicarbazone)
  • Carbon
  • Copper