Abstract

Background 211At-labeled radiopharmaceuticals are potentially useful for tumor therapy. However, a limitation has been the preferential accumulation of released 211At in the thyroid gland, which is a critical organ for such therapy. The aim of this study was to determine the effect of absorbed dose, dose-rate, and time after 211At exposure on genome-wide transcriptional expression in mouse thyroid gland.MethodsBALB/c mice were i.v. injected with 1.7, 7.5 or 100 kBq 211At. Animals injected with 1.7 kBq were killed after 1, 6, or 168 h with mean thyroid absorbed doses of 0.023, 0.32, and 1.8 Gy, respectively. Animals injected with 7.5 and 100 kBq were killed after 6 and 1 h, respectively; mean thyroid absorbed dose was 1.4 Gy. Total RNA was extracted from pooled thyroids and the Illumina RNA microarray platform was used to determine mRNA levels. Differentially expressed transcripts and enriched GO terms were determined with adjusted p-value <0.01 and fold change >1.5, and p-value <0.05, respectively.ResultsIn total, 1232 differentially expressed transcripts were detected after 211At administration, demonstrating a profound effect on gene regulation. The number of regulated transcripts increased with higher initial dose-rate/absorbed dose at 1 or 6 h. However, the number of regulated transcripts decreased with mean absorbed dose/time after 1.7 kBq 211At administration. Furthermore, similar regulation profiles were seen for groups administered 1.7 kBq. Interestingly, few previously proposed radiation responsive genes were detected in the present study. Regulation of immunological processes were prevalent at 1, 6, and 168 h after 1.7 kBq administration (0.023, 0.32, 1.8 Gy).

Highlights

  • Cellular responses to stimuli can be studied on different molecular levels, including gene expression regulation

  • The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript

  • Calculation of absorbed dose from alpha particles emitted by 211At and its daughter nuclide 211Po located in the thyroid using the Medical Internal Radiation Dose (MIRD) formalism has been previously described [11, 18]. 211At decays to either 211Po (58%) by electron capture (EC) or to 207Bi (42%) by emission of mainly 5.87 MeV α-particles [19]. 211Po quickly (t1⁄2: 0.52 s) decays to 207Pb with emission of mainly 7.45 MeV α-particles, while 207Bi decays much slower (t1⁄2: 31.5 y) by EC to 207Pb

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Summary

Introduction

Cellular responses to stimuli can be studied on different molecular levels, including gene expression regulation. By comparing genome-wide transcriptional levels between samples, e.g. irradiated and non-irradiated thyroids, a differential gene expression profile can be generated illustrating gene up- and downregulation for each tissue sample. This technique allows for the assessment of changes in cellular activity due to radiation exposure and facilitates the identification of radiation biomarkers [1]. During metabolism of 211At-labeled radiopharmaceuticals, free 211At may be released, resulting in significant thyroid gland exposure [6]. The aim of this study was to determine the effect of absorbed dose, dose-rate, and time after 211At exposure on genome-wide transcriptional expression in mouse thyroid gland

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