首页> 外文期刊>Journal of Agricultural and Food Chemistry >Water Stress Proteins from Nostoc commune Vauch. Exhibit Anti-Colon Cancer Activities in Vitro and in Vivo
【24h】

Water Stress Proteins from Nostoc commune Vauch. Exhibit Anti-Colon Cancer Activities in Vitro and in Vivo

机译:来自Nostoc公社的水分胁迫蛋白。体内和体外展示抗结肠癌活性

获取原文
获取原文并翻译 | 示例
       

摘要

Nostoc commune has been traditionally used in China as a health food and medicine. The water stress proteins (WSP) of Nostoc commune are the major component of the extracellular matrix. This study purified and identified the water stress proteins (WSP1) from Nostoc commune Vauch., which could inhibit the proliferation of human colon cancer cell lines. The IC50 values of WSP1 against DLD1, HCT116, HT29, and SW480 cells were 0.19 +/- 0.02, 0.21 +/- 0.03, 0.39 +/- 0.05, and 0.41 +/- 0.01 mu g/mu L, respectively. Notably, it displayed very little effect on the normal human intestinal epithelial FHC cell line. The IC50 value of WSP1 against FHC cells was 0.67 +/- 0.05 mu g/mu L. Moreover, the growth of DLD1 xenografted tumors in nude mice were significantly suppressed in the WSP1 treated group. Mechanistically, the cell-cycle analysis revealed that WSP1 induced growth inhibition by G1/S arrest. Meanwhile, Western blotting and immunohistochemistry assays showed WSP1 could activate caspase-8, -9, and -3, along with subsequent PARP cleavage. Furthermore, the pan-caspase inhibitor, z-VAD-FMK, partly reversed the effect caused by WSP1, confirming that WSP1 induced cell apoptosis through caspase-dependent pathway. Collectively, WSP1 has targeted inhibition for colon cancer proliferation both in vitro and in vivo and it is valuable for future exploitation and utilization as an antitumor agent.
机译:诺斯托克公社在中国传统上用作保健食品和药品。 Nostoc社的水分胁迫蛋白(WSP)是细胞外基质的主要成分。本研究从Nostoc公社Vauch中纯化并鉴定了水分胁迫蛋白(WSP1),它可以抑制人结肠癌细胞系的增殖。 WSP1对DLD1,HCT116,HT29和SW480细胞的IC50值分别为0.19 +/- 0.02、0.21 +/- 0.03、0.39 +/- 0.05和0.41 +/- 0.01μg /μL。值得注意的是,它对正常人肠道上皮FHC细胞系的作用很小。 WSP1对FHC细胞的IC50值为0.67 +/- 0.05μg/μL。此外,在WSP1治疗组中,裸鼠中DLD1异种移植肿瘤的生长受到显着抑制。从机理上讲,细胞周期分析表明WSP1通过G1 / S阻滞诱导生长抑制。同时,Western印迹和免疫组织化学分析表明WSP1可以激活caspase-8,-9和-3以及随后的PARP裂解。此外,泛半胱天冬酶抑制剂z-VAD-FMK可部分逆转WSP1引起的效应,证实WSP1通过caspase依赖性途径诱导细胞凋亡。总体而言,WSP1在体外和体内均具有针对结肠癌增殖的靶向抑制作用,对于将来作为抗肿瘤剂的开发和利用具有重要意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号