4.3 Article

Time- and dose rate-related effects of internal 177Lu exposure on gene expression in mouse kidney tissue

Journal

NUCLEAR MEDICINE AND BIOLOGY
Volume 41, Issue 10, Pages 825-832

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.nucmedbio.2014.07.010

Keywords

Radiation biology; Lutetium-177; Microarray; Kidney toxicity

Funding

  1. Swedish Research Council [21073]
  2. Swedish Cancer Society [3427]
  3. BioCARE - National Strategic Research Program at the University of Gothenburg
  4. King Gustav V jubilee Clinic Cancer Research Foundation
  5. Sahlgrenska University Hospital Research Funds
  6. Assar Gabrielsson Cancer Research Foundation
  7. Lions Cancer Research Foundation West
  8. Wilhelm and Martina Lundgrens science fund
  9. Adlerbertska Research Foundation

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Introduction: The kidneys are the dose-limiting organs in some radionuclide therapy regimens. However, the biological impact of internal exposure from radionuclides is still not fully understood. The aim of this study was to examine the effects of dose rate and time after i.v. injection of (LuCl3)-Lu-177 on changes in transcriptional patterns in mouse kidney tissue. Methods: To investigate the effect of dose rate, female Balb/c nude mice were i.v. injected with 11, 5.6, 1.6, 0.8, 0.30, and 0 MBq of (LuCl3)-Lu-177, and killed at 3, 6, 24, 48, 168, and 24 hours after injection, respectively. Furthermore, the effect of time after onset of exposure was analysed using mice injected with 0.26, 2.4, and 8.2 MBq of (LuCl3)-Lu-177, and killed at 45, 90, and 140 days after injection. Global transcription patterns of irradiated kidney cortex and medulla were assessed and enriched biological processes were determined from the regulated gene sets using Gene Ontology terms. Results: The average dose rates investigated were 1.6, 0.84, 0.23, 0.11 and 0.028 mGy/min, with an absorbed dose of 0.3 Gy. At 45,90 and 140 days, the absorbed doses were estimated to 0.3, 3, and 10 Gy. In general, the number of differentially regulated transcripts increased with time after injection, and decreased with absorbed dose for both kidney cortex and medulla. Differentially regulated transcripts were predominantly involved in metabolic and stress response-related processes dependent on dose rate, as well as transcripts associated with metabolic and cellular integrity at later time points. Conclusion: The observed transcriptional response in kidney tissue was diverse due to difference in absorbed dose, dose rate and time after exposure. Nevertheless, several transcripts were significantly regulated in all groups despite differences in exposure parameters, which may indicate potential biomarkers for exposure of kidney tissue. (c) 2014 Elsevier Inc. All rights reserved.

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