Administration of TGF-ss Inhibitor Mitigates Radiation-induced Fibrosis in a Mouse Model

被引:9
|
作者
Gans, Itai [1 ]
El Abiad, Jad M. [1 ]
James, Aaron W. [2 ]
Levin, Adam S. [1 ]
Morris, Carol D. [1 ,3 ,4 ]
机构
[1] Johns Hopkins Univ, Dept Orthopaed Surg, Sch Med, Baltimore, MD USA
[2] Johns Hopkins Univ, Sch Med, Ross Res Bldg, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ Hosp, Dept Orthopaed Surg, Div Orthopaed Oncol, 601 North Caroline St, Baltimore, MD 21287 USA
关键词
GROWTH-FACTOR-BETA; MOLECULAR-MECHANISMS; I COLLAGEN; SKIN; IRRADIATION; EXPRESSION; ACTIVATION; ANTIBODIES; WOUNDS; INJURY;
D O I
10.1097/CORR.0000000000001286
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background Radiation-induced fibrosis is a long-term adverse effect of external beam radiation therapy for cancer treatment that can cause pain, loss of function, and decreased quality of life. Transforming growth factor beta (TGF-beta) is believed to be critical to the development of radiation-induced fibrosis, and TGF-beta inhibition decreases the development of fibrosis. However, no treatment exists to prevent radiation-induced fibrosis. Therefore, we aimed to mitigate the development of radiation-induced fibrosis in a mouse model by inhibiting TGF-beta. Question/purposes Does TGF-beta inhibition decrease the development of muscle fibrosis induced by external beam radiation in a mouse model? Methods Twenty-eight 12-week-old male C57BL/6 mice were assigned randomly to three groups: irradiated mice treated with TGF-beta i, irradiated mice treated with placebo, and control mice that received neither irradiation nor treatment. The irradiated mice received one 50-Gy fraction of radiation to the right hindlimb before treatment initiation. Mice treated with TGF-c (n = 10) received daily intraperitoneal injections of a small-molecule inhibitor of TGF-beta (1 mg/kg) in a dimethyl sulfoxide vehicle for 8 weeks (seven survived to histologic analysis). Mice treated with placebo (n = 10) received daily intraperitoneal injections of only a dimethyl sulfoxide vehicle for 8 weeks (10 survived to histologic analysis). Control mice (n = 8) received neither radiation nor TGF-beta treatment. Control mice were euthanized at 3 months because they were not expected to exhibit any changes related to treatment. Mice in the two treatment groups were euthanized 9 months after radiation, and the quadriceps of each thigh was sampled. Masson's trichome stain was used to assess muscle fibrosis. Slides were viewed at 10 x magnification using bright-field microscopy, and in a blinded fashion, five representative images per mouse were used to quantify fibrosis. The mean +/- SD fibrosis pixel densities in the TGF-beta i and radiation-only groups were compared using Mann-Whitney U tests. The ratio of fibrosis to muscle was calculated using the mean fibrosis per slide in the TGF-beta i group to standardize measurements. Alpha was set at 0.05. Results The mean (+/- SD) percentage of fibrosis per slide was greater in the radiation-only group (1.2% +/- 0.42%) than in the TGF-beta i group (0.14% +/- 0.09%) (odds ratio 0.12 [95% CI 0.07 to 0.20]; p < 0.001). Among control mice, mean fibrosis was 0.05% +/- 0.02% per slide. Mice in the radiation-only group had 9.1 times the density of fibrosis as did mice in the TGF-beta i group. Conclusion Our study provides preliminary evidence that the fibrosis associated with radiation therapy to a quadriceps muscle can be reduced by treatment with a TGF-beta inhibitor in a mouse model.
引用
收藏
页码:468 / 474
页数:7
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