Department of a Urology, Shaanxi Provincial People's Hospital, Xi'an 710068, China.
Xi'an Medical University, Xi'an 710068, China.
Radiat Res. 2021 May 1;195(5):452-462. doi: 10.1667/RADE-20-00239.1.
The goals of this study were to determine whether curcumin can radiosensitize human urethral scar fibroblasts (HUSFs) and inhibit the synthesis of collagen, and to explore the molecular mechanism. Here, HUSFs were established and cultured in vitro and cell counting kit-8 (CCK-8) experiment and plate clone formation assay were performed to determine the appropriate concentration of curcumin and radiation dose. The radiosensitization of curcumin was confirmed by plate clone formation assay. Cell cycle distribution was determined by flow cytometry and apoptosis rate by TdT-mediated dUTP nick-end labeling (TUNEL). Western blot was used to detect the levels of collagen I, collagen III, Smad2, Smad3, Smad4, transforming growth factor-β (TGF-β1), Beclin1 and microtubule-associated protein light chain 3 (LC3), as a means of determining the mechanism. Our findings showed that curcumin enhanced radiosensitivity of HUSFs in vitro (sensitization enhancement ratio = 2.030). Furthermore, curcumin and radiation treatments promoted the apoptosis of HUSFs and blocked the cells in G2/M phase. In addition, curcumin combined with radiation inhibited the synthesis of collagen I and collagen III through Smad4 pathway, with possible involvement of autophagy. These results suggest that curcumin could be a radiosensitizer of HUSFs, inhibit the proliferation of HUSFs and suppress fibrosis by downregulation of Smad4 via autophagy.
本研究旨在探讨姜黄素能否放射增敏人尿道瘢痕成纤维细胞(HUSFs)并抑制胶原合成,并探索其分子机制。体外培养 HUSFs,采用细胞计数试剂盒(CCK-8)实验和平板克隆形成实验确定姜黄素的适宜浓度和辐射剂量。平板克隆形成实验证实了姜黄素的放射增敏作用。通过流式细胞术检测细胞周期分布,通过末端转移酶介导的 dUTP 缺口末端标记(TUNEL)法检测细胞凋亡率。采用 Western blot 检测 I 型和 III 型胶原、Smad2、Smad3、Smad4、转化生长因子-β(TGF-β1)、Beclin1 和微管相关蛋白轻链 3(LC3)的水平,以确定其机制。结果表明,姜黄素增强了 HUSFs 的体外放射敏感性(增敏比=2.030)。此外,姜黄素和辐射处理促进了 HUSFs 的凋亡,并阻止细胞进入 G2/M 期。此外,姜黄素联合辐射通过自噬抑制 Smad4 通路抑制 I 型和 III 型胶原的合成。这些结果表明,姜黄素可能通过自噬下调 Smad4 来增敏 HUSFs,抑制 HUSFs 的增殖并抑制纤维化。