National Engineering Laboratory for Modern Silk, College of Textile and Clothing Engineering, Soochow University, Suzhou, 215123, P. R. China.
Department of Colorectal Surgery, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510655, China.
Adv Healthc Mater. 2018 Dec;7(24):e1801213. doi: 10.1002/adhm.201801213. Epub 2018 Nov 23.
In-stent restenosis caused by tumor ingrowth is a major problem for patients undergoing stent placement because conventional stents often lack sustainable antitumor capabilities. The aim of this work is to develop a silk fibroin (SF)-based nanofibrous membrane that is loaded with combined-therapy drugs by using electrospinning technologies, which is further coated on a polydioxanone (PDO) stent and used for the treatment of colorectal cancer (CRC). In order to improve treatment effectiveness, a combination of therapeutic drugs, i.e., curcumin (CUR) and 5-fluorouracil (5-FU), is dissolved into SF solution and then eletrospun onto the surface of the PDO stent. The morphology, secondary structure, and in vitro drug release profiles of the membranes are characterized. The antitumor efficacy is assessed in vitro and in vivo using a human CRC cell line and normal cells, and tumor-bearing nude mice. In vitro and in vivo studies on the nanofibrous memembrane-coating demonstrate improved antitumor effects for the CUR/5-FU dual drug system which can be attributed to cell cycle arrest in the S phase in association with induced apoptosis in tumor cells by blocking signal transducer and activator of transcription3 (Stat3) and nuclear factor kappa beta (NF-kB) signaling pathways, suggesting potential in the treatment of CRC in the future.
支架内再狭窄是接受支架置入术患者的一个主要问题,因为传统支架往往缺乏可持续的抗肿瘤能力。本工作旨在开发一种载有联合治疗药物的丝素(SF)纳米纤维膜,采用静电纺丝技术将其负载到聚二氧杂环已酮(PDO)支架上,用于治疗结直肠癌(CRC)。为了提高治疗效果,将两种治疗药物,即姜黄素(CUR)和 5-氟尿嘧啶(5-FU)溶解在 SF 溶液中,然后静电纺到 PDO 支架的表面。对膜的形态、二级结构和体外药物释放曲线进行了表征。采用人结直肠癌细胞系和正常细胞以及荷瘤裸鼠进行体外和体内抗肿瘤功效评估。对纳米纤维膜涂层的体外和体内研究表明,CUR/5-FU 双药物系统具有更好的抗肿瘤效果,这归因于通过阻断信号转导和转录激活因子 3(Stat3)和核因子 kappa beta(NF-kB)信号通路,使肿瘤细胞的 S 期细胞周期停滞并诱导细胞凋亡,提示其在未来 CRC 治疗中的潜力。