Ultrastructural Analysis of Cancer Cells Treated with the Radiopharmaceutical Radium Dichloride ([223Ra]RaCl2): Understanding the Effect on Cell Structure

Author:

Diniz Filho Joel Félix Silva1,de Barros Aline Oliveira da Silva2,Pijeira Martha Sahylí Ortega2ORCID,Ricci-Junior Eduardo3ORCID,Midlej Victor4ORCID,Baroni Mariana Pelissari Monteiro Aguiar5ORCID,dos Santos Clenilton Costa1,Alencar Luciana Magalhães Rebelo1ORCID,Santos-Oliveira Ralph26ORCID

Affiliation:

1. Biophysics and Nanosystems Laboratory, Department of Physics, Federal University of Maranhão, São Luis 65065690, MA, Brazil

2. Laboratory of Nanoradiopharmacy and Synthesis of New Radiopharmaceuticals, Brazilian Nuclear Energy Commission, Nuclear Engineering Institute, Rio de Janeiro 21941906, RJ, Brazil

3. School of Pharmacy, Federal University of Rio de Janeiro, Rio de Janeiro 21941900, RJ, Brazil

4. Laboratory of Structural Biology, Oswaldo Cruz Institute (FIOCRUZ), Rio de Janeiro 21040900, RJ, Brazil

5. Department of Natural Science and Mathematics, Federal Institute of Education, Science and Technology (IFSP), Campus São Paulo, São Paulo 01109010, SP, Brazil

6. Laboratory of Radiopharmacy and Nanoradiopharmaceuticals, State University of Rio de Janeiro, Rio de Janeiro 23070200, RJ, Brazil

Abstract

The use of alpha-particle (α-particle) radionuclides, especially [223Ra]RaCl2 (radium dichloride), for targeted alpha therapy is steadily increasing. Despite the positive clinical outcomes of this therapy, very little data are available about the effect on the ultrastructure of cells. The purpose of this study was to evaluate the nanomechanical and ultrastructure effect of [223Ra] RaCl2 on cancer cells. To analyze the effect of [223Ra]RaCl2 on tumor cells, human breast cancer cells (lineage MDA-MB-231) were cultured and treated with the radiopharmaceutical at doses of 2 µCi and 0.9 µCi. The effect was evaluated using atomic force microscopy (AFM) and transmission electron microscopy (TEM) combined with Raman spectroscopy. The results showed massive destruction of the cell membrane but preservation of the nucleus membrane. No evidence of DNA alteration was observed. The data demonstrated the formation of lysosomes and phagosomes. These findings help elucidate the main mechanism involved in cell death during α-particle therapy.

Funder

Carlos Chagas Filho Foundation for Research Support of Rio de Janeiro State

CNPq

National Nuclear Energy Commission

Publisher

MDPI AG

Subject

General Medicine

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