Pharmacological induction of transforming growth factor-beta1 in rat models enhances radiation injury in the intestine and the heart.

Radiation therapy in the treatment of cancer is dose limited by radiation injury in normal tissues such as the intestine and the heart. To identify the mechanistic involvement of transforming growth factor-beta 1 (TGF-β1) in intestinal and cardiac radiation injury, we studied the influence of pharma...

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Main Authors: Marjan Boerma, Junru Wang, Vijayalakshmi Sridharan, Jean-Marc Herbert, Martin Hauer-Jensen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3723823?pdf=render
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author Marjan Boerma
Junru Wang
Vijayalakshmi Sridharan
Jean-Marc Herbert
Martin Hauer-Jensen
author_facet Marjan Boerma
Junru Wang
Vijayalakshmi Sridharan
Jean-Marc Herbert
Martin Hauer-Jensen
author_sort Marjan Boerma
collection DOAJ
description Radiation therapy in the treatment of cancer is dose limited by radiation injury in normal tissues such as the intestine and the heart. To identify the mechanistic involvement of transforming growth factor-beta 1 (TGF-β1) in intestinal and cardiac radiation injury, we studied the influence of pharmacological induction of TGF-β1 with xaliproden (SR 57746A) in rat models of radiation enteropathy and radiation-induced heart disease (RIHD). Because it was uncertain to what extent TGF-β induction may enhance radiation injury in heart and intestine, animals were exposed to irradiation schedules that cause mild to moderate (acute) radiation injury. In the radiation enteropathy model, male Sprague-Dawley rats received local irradiation of a 4-cm loop of rat ileum with 7 once-daily fractions of 5.6 Gy, and intestinal injury was assessed at 2 weeks and 12 weeks after irradiation. In the RIHD model, male Sprague-Dawley rats received local heart irradiation with a single dose of 18 Gy and were followed for 6 months after irradiation. Rats were treated orally with xaliproden starting 3 days before irradiation until the end of the experiments. Treatment with xaliproden increased circulating TGF-β1 levels by 300% and significantly induced expression of TGF-β1 and TGF-β1 target genes in the irradiated intestine and heart. Various radiation-induced structural changes in the intestine at 2 and 12 weeks were significantly enhanced with TGF-β1 induction. Similarly, in the RIHD model induction of TGF-β1 augmented radiation-induced changes in cardiac function and myocardial fibrosis. These results lend further support for the direct involvement of TGF-β1 in biological mechanisms of radiation-induced adverse remodeling in the intestine and the heart.
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spelling doaj.art-6da39585fb8649a3ac7795f76dbb4dc82022-12-21T18:41:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0187e7047910.1371/journal.pone.0070479Pharmacological induction of transforming growth factor-beta1 in rat models enhances radiation injury in the intestine and the heart.Marjan BoermaJunru WangVijayalakshmi SridharanJean-Marc HerbertMartin Hauer-JensenRadiation therapy in the treatment of cancer is dose limited by radiation injury in normal tissues such as the intestine and the heart. To identify the mechanistic involvement of transforming growth factor-beta 1 (TGF-β1) in intestinal and cardiac radiation injury, we studied the influence of pharmacological induction of TGF-β1 with xaliproden (SR 57746A) in rat models of radiation enteropathy and radiation-induced heart disease (RIHD). Because it was uncertain to what extent TGF-β induction may enhance radiation injury in heart and intestine, animals were exposed to irradiation schedules that cause mild to moderate (acute) radiation injury. In the radiation enteropathy model, male Sprague-Dawley rats received local irradiation of a 4-cm loop of rat ileum with 7 once-daily fractions of 5.6 Gy, and intestinal injury was assessed at 2 weeks and 12 weeks after irradiation. In the RIHD model, male Sprague-Dawley rats received local heart irradiation with a single dose of 18 Gy and were followed for 6 months after irradiation. Rats were treated orally with xaliproden starting 3 days before irradiation until the end of the experiments. Treatment with xaliproden increased circulating TGF-β1 levels by 300% and significantly induced expression of TGF-β1 and TGF-β1 target genes in the irradiated intestine and heart. Various radiation-induced structural changes in the intestine at 2 and 12 weeks were significantly enhanced with TGF-β1 induction. Similarly, in the RIHD model induction of TGF-β1 augmented radiation-induced changes in cardiac function and myocardial fibrosis. These results lend further support for the direct involvement of TGF-β1 in biological mechanisms of radiation-induced adverse remodeling in the intestine and the heart.http://europepmc.org/articles/PMC3723823?pdf=render
spellingShingle Marjan Boerma
Junru Wang
Vijayalakshmi Sridharan
Jean-Marc Herbert
Martin Hauer-Jensen
Pharmacological induction of transforming growth factor-beta1 in rat models enhances radiation injury in the intestine and the heart.
PLoS ONE
title Pharmacological induction of transforming growth factor-beta1 in rat models enhances radiation injury in the intestine and the heart.
title_full Pharmacological induction of transforming growth factor-beta1 in rat models enhances radiation injury in the intestine and the heart.
title_fullStr Pharmacological induction of transforming growth factor-beta1 in rat models enhances radiation injury in the intestine and the heart.
title_full_unstemmed Pharmacological induction of transforming growth factor-beta1 in rat models enhances radiation injury in the intestine and the heart.
title_short Pharmacological induction of transforming growth factor-beta1 in rat models enhances radiation injury in the intestine and the heart.
title_sort pharmacological induction of transforming growth factor beta1 in rat models enhances radiation injury in the intestine and the heart
url http://europepmc.org/articles/PMC3723823?pdf=render
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