Mapping genetic modifiers of radiation-induced cardiotoxicity to rat chromosome 3.

Authors:
Anne Frei
Anne Frei
From the Cancer Center
Shirng-Wern Tsaih
Shirng-Wern Tsaih
Medical College of Wisconsin
United States
Brian L Fish
Brian L Fish
Medical College of Wisconsin
Madison | United States
Leanne Harmann
Leanne Harmann
Medical College of Wisconsin
United States
Qian Liu
Qian Liu
State Key Laboratory of Environmental Chemistry and Ecotoxicology
China

Am J Physiol Heart Circ Physiol 2019 Jun 8;316(6):H1267-H1280. Epub 2019 Mar 8.

Department of Radiation Oncology, Medical College of Wisconsin , Milwaukee, Wisconsin.

Radiation therapy is used in ~50% of cancer patients to reduce the risk of recurrence and in some cases improve survival. Despite these benefits, doses can be limited by toxicity in multiple organs, including the heart. The underlying causes and biomarkers of radiation-induced cardiotoxicity are currently unknown, prompting the need for experimental models with inherent differences in sensitivity and resistance to the development of radiation-induced cardiotoxicity. We have identified the parental SS (Dahl salt-sensitive/Mcwi) rat strain to be a highly-sensitized model of radiation-induced cardiotoxicity. In comparison, substitution of rat chromosome 3 from the resistant BN (Brown Norway) rat strain onto the SS background (SS-3 consomic) significantly attenuated radiation-induced cardiotoxicity. SS-3 rats had less radiation-induced cardiotoxicity than SS rats, as measured by survival, pleural and pericardial effusions, echocardiogram parameters, and histological damage. Mast cells, previously shown to have predominantly protective roles in radiation-induced cardiotoxicity, were increased in the more resistant SS-3 hearts postradiation. RNA sequencing from SS and SS-3 hearts at 1 wk postradiation revealed 5,098 differentially expressed candidate genes across the transcriptome and 350 differentially expressed genes on rat chromosome 3, which coincided with enrichment of multiple pathways, including mitochondrial dysfunction, sirtuin signaling, and ubiquitination. Upstream regulators of enriched pathways included the oxidative stress modulating transcription factor, , which is located on rat chromosome 3. target genes were also differentially expressed in the SS vs. SS-3 consomic hearts postradiation. Collectively, these data confirm the existence of heritable modifiers in radiation-induced cardiotoxicity and provide multiple biomarkers, pathways, and candidate genes for future analyses. This novel study reveals that heritable genetic factors have the potential to modify normal tissue sensitivity to radiation. Gene variant(s) on rat chromosome 3 can contribute to enhanced cardiotoxicity displayed in the SS rats vs. the BN and SS-3 consomic rats. Identifying genes that lead to understanding the mechanisms of radiation-induced cardiotoxicity represents a novel method to personalize radiation treatment, as well as predict the development of radiation-induced cardiotoxicity.

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Source
http://dx.doi.org/10.1152/ajpheart.00482.2018DOI Listing
June 2019
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