Tamoxifen citrate: a glimmer of hope for silicosis

被引:8
作者
Yoldas, Omer [1 ]
Karaca, Turgut [2 ]
Bilgin, Bulent Caglar [3 ]
Yilmaz, Omer Hinc [4 ]
Simsek, Gulcin Guler [5 ]
Alici, Ibrahim Onur [6 ]
Uzdogan, Andac [7 ]
Karaca, Nihal [8 ]
Akin, Tezcan [9 ]
Yoldas, Suna [10 ]
Akbiyik, Filiz [11 ,12 ]
机构
[1] Izmir Univ, Fac Med, Dept Gen Surg, TR-35510 Karsiyaka Izmir, Turkey
[2] Iskenderun State Hosp, Dept Gen Surg, Iskenderun, Turkey
[3] Kafkas Univ, Dept Gen Surg, Fac Med, Kars, Turkey
[4] Ankara Occupat Dis Hosp, Dept Toxicol, Ankara, Turkey
[5] Kecioren Educ & Res Hosp, Dept Pathol, Ankara, Turkey
[6] Ankara Occupat Dis Hosp, Dept Pulmonol, Ankara, Turkey
[7] Hacettepe Univ, Fac Med, Dept Med Biochem, TR-06100 Ankara, Turkey
[8] Ankara Univ, Dept Anesthesiol & Reanimat, Fac Med, TR-06100 Ankara, Turkey
[9] Ankara Numune Training & Res Hosp, Ankara, Turkey
[10] Hosp Pediat Dis, Dept Anesthesiol, Izmir, Turkey
[11] Hacettepe Univ, Fac Med, Dept Biochem, TR-06100 Ankara, Turkey
[12] Hacettepe Univ Hosp, Clin Pathol Lab, Ankara, Turkey
关键词
Silicosis; Tamoxifen; Treatment; Fibrosis; TGF-beta; GROWTH-FACTOR-BETA; RAT MODEL; CANCER CELLS; IN-VITRO; FIBROSIS; PROLIFERATION;
D O I
10.1016/j.jss.2014.08.013
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Inhalation of crystalline silica nanoparticles causes pulmonary damage resulting in progressive lung fibrosis. Currently, there is no effective treatment for silicosis. Tamoxifen citrate is a selective estrogen receptor modulator, which is one of the adjuvant treatment choices for breast cancer. It is also known with its inhibitory effect on the production of transforming growth factor-beta (TGF-beta) and studied for the anti-fibrotic effect in some fibrotic diseases. The aim of the study was to determine the effect of tamoxifen citrate on the prevention of pulmonary fibrosis and the treatment of silicosis. Methods: A total of 100 adult female Wistar Albino rats (200-250 g) were used in this study. The rats were divided into five groups including 20 rats in each. Rats were exposed to silica for 84 d in all groups. In group 1, rats were sacrificed on the day 84 without receiving treatment. In group 2, rats received 1 mg/kg tamoxifen (tmx1 + 1), from the first day of the study for the whole 114 d of the study. In group 3, (tmx10 + 10) rats were given 10 mg/kg tamoxifen from the first day of the study for the whole 114 d of the study. In group 4 (tmx1), rats were started 1 mg/kg of tamoxifen on day 84 and were given until day 114. In group 5 (tmx10), rats were fed with 10 mg/kg tamoxifen starting from day 84 to day 114. All rats except group 1 were sacrificed on 114 day of the study. Lung inflammation and fibrosis scores, serum TGF beta levels, lung smooth muscle antigen and tissue transforming growth factor beta (t-TGF-beta) antibody staining levels, and number of silicotic rats were compared between groups. Results: Silicosis was caused successfully in all rats in group 1. There were six silicotic rats in group 3 and it was the lowest number of all groups. Plasma TGF-beta levels and fibrosis score were significantly lower in all groups when compared with the control group. Tamoxifen could have preventive or treating effects in silicosis and found that lung fibrosis score was significantly lower in rats treated with tamoxifen. Conclusions: Tamoxifen treatment after and/or before induction of silicosis decreased lung fibrosis score with blood TGF-beta levels. We hope that this study may introduce a new indication as prophylactic use of tamoxifen in high-risk groups for silicosis and for treatment of silicosis. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:429 / 434
页数:6
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