期刊文献+

成纤维细胞分泌TIMP-1抑制小鼠黑色素瘤细胞浸润和转移 被引量:3

TIMP-1 Secreted by Fibroblasts Inhibits Tumor Cell Invasion and Metastasis in Mouse Melanoma
原文传递
导出
摘要 构建含人金属蛋白酶-1组织抑制剂(TIMP-1)基因的重组腺病毒载体(Ad-TIMP-1)。通过Ad-TIMP-1感染原代培养的小鼠成纤维细胞,研究Ad-TIMP-1成纤维细胞对小鼠黑色素瘤细胞浸润和转移的影响。结果显示,Ad-TIMP-1原代成纤维细胞能有效表达并分泌TIMP-1;其分泌的TIMP-1可以在体内和体外显著抑制小鼠黑色素瘤B16BL6细胞的浸润和转移;皮下注射Ad-TIMP-1原代成纤维细胞制剂到小鼠体内,可以分泌TIMP-1进入小鼠血液中并维持较高水平。提示,腺病毒介导的分泌型TIMP-1原代成纤维细胞制剂可以为临床治疗肿瘤转移提供一种新的基因治疗手段,具有潜在临床应用价值。 We constructed a recombinant adenoviral vector expressing human tissue inhibitors of metalloproteinase-1 (TIMP-1), and evaluated the inhibition of TIMP-1 secreted by primary fibroblasts after infection with adenovirus-mediated TIMP-1 gene(Ad-TIMP-1) on tumor cell invasion and metastasis in mouse melanoma. It was found that TIMP-1 was dectected in the supernatants of cultured mouse primary fibroblasts after infection with Ad-TIMP- 1 by indirect enzyme-linked immunosorbent assay {ELISA). The TIMP-1 secreted by Ad-TIMP-1 infected primary fibroblast significantly inhibited B16BL6 cell invasion and metastasis both in vitro and in vivo. We also demonstrated that the primary fibroblasts transfeeted by Ad-TIMP-1, after being subcutaneously injected into mouse~ can secreted TIMP-1 into the blood of mouse and maintained at the therapeutic in vivo levels of TIMP-1. These results suggest that the preparation of Ad-TIMP-1 infected primary fibroblast be an effective method to deliver TIMP-1 gene in vivo, which provids a new strategy of gene therapy and has the potential for clinical applications in the treatment of tumor cell metastasis
出处 《生物医学工程学杂志》 EI CAS CSCD 北大核心 2009年第3期610-614,共5页 Journal of Biomedical Engineering
基金 扬州大学生命科学学科群项目资助
关键词 金属蛋白酶-1组织抑制剂 重组腺病毒 成纤维细胞 黑色素瘤 转移 Tissue inhibitors of metalloproteinase-1 (TIMP-1) Recombinant adenovirus Primary fibro- blast Melanoma Metastasis
  • 相关文献

参考文献11

  • 1TSUBAKI M, MATSUOKA H, YAMAMOTO C, et al.The protein kinase C inhibitor, H7, inhibits tumor cell invasion and metastasis in mouse melanoma via suppression of ERK1/2[J]. C/in Exp Metastasis, 2007, 24(6):431-438. 被引量:1
  • 2NIKKOLA J, VIHINEN P, VUORISTO M S, et al. High serum levels of matrix metalloproteinase-9 and matrix metalloproteinase-1 are associated with rapid progression in patients with metastatic melanoma[J]. Clin Cancer Res, 2005, 11 (14) :5158-5166. 被引量:1
  • 3ECCLES SA. Parallels in invasion and angiogenesis provide pivotal points for therapeutic intervention[J]. Int J Dev Biol, 2004, 48(5-6) :583-598. 被引量:1
  • 4GUO S Y, SHEN X, YANG J, et al. TIMP-1 mediates the inhibitory effect of interleukin-6 on the proliferation of a hepatocarcinoma cell line in a STAT3-dependent manner[J]. Braz J Med Biol Res, 2007, 40(5):621-631. 被引量:1
  • 5ZATLOUKAL K, COTTEN M, BERGER M, et al. In vivo production of human factor Ⅶ in mice after intrasplenie implantation of primary fibroblasts transfected by receptor-mediated, adenovirus-augmented gene delivery[J]. Proc Natl Aead Sci USA, 1994, 91(11):5148-5152. 被引量:1
  • 6HE T C, ZHOU S, da COSTA L T, et al. A simplified system for generating recombinant adenoviruses[J]. Proc Natl Acad Sci USA, 1998, 95(5):2509-2514. 被引量:1
  • 7SHEN W G, XUE Q Y, WU Y D, et al. Melanoma-associated antigen family protein-D1 regulation of tumor cell migration, adhesion to endothelium, and actin structures reorganization in response to hypoxic stress[J]. Cell Commun Adhes, 2007, 14 (1):21-31 mice after. 被引量:1
  • 8MILLER A J, MIHM M C. Melanoma[J]. N Engl J Med, 2006, 355(1):51-65. 被引量:1
  • 9HOFMANN U B, WESTPHAL J R, VAN MUIJEN G N, et al. Matrix metalloproteinases in human melanoma[J]. J Invest Dermatol, 2000, 115(3) :337-344. 被引量:1
  • 10ZUCKER S, CAO J, CHEN W T. Critical appraisal of the use of matrix metalloproteinase inhibitors in cancer treatment [J]. Oneogene, 2000, 19(56):6642-6650. 被引量:1

同被引文献35

  • 1朱松柏,吕永曼.金雀异黄素抗癌作用分子机制研究进展[J].华中医学杂志,2006,30(3):253-254. 被引量:11
  • 2阿克曼.阿克曼外科病理学.回允中主译.北京:北京大学出版社,2006.1269. 被引量:2
  • 3MILLER A J,MIHN M C J R.Melanoma[J].N Engl J Med,2006,355(1):51-65. 被引量:1
  • 4POLKOWSKI K,MAZUREK A P.Biological properties of genistein.a review of in vitro and in vivo data[J].Acta Polonica Pharmacology,2000,57(2):135-155. 被引量:1
  • 5CHODON D,RAMAMURTY N,SAKTHISEKARAN D.Preliminary studies on induction of apoptosis by genistein on HepG2 cell line[J].Toxicol In Vitro,2007,21(5):887-891. 被引量:1
  • 6MATSUKAWA Y,MARUI N,SAKAI T,et al.Genistein arrests cell cycle progression at G2/M[J].Cancer Res,1993,53(6):1328-1331. 被引量:1
  • 7SARKAR F H,LI Yiwei.Mechanisms of cancer chemoprevention by soy isoflavone genistein[J].Cancer Metastasis Rev,2002,21(3/4):265-280. 被引量:1
  • 8AIHARA M,SUGAWARA K,TORII S,et al.Angiogenic endothelium-specific nestin expression is enhanced by the first intron of the nestin gene[J].Lab Invest,2004,84(12):1581-1592. 被引量:1
  • 9SHEN Weigan,XUE Qingyu,WU Yiding,et al.Melanoma-associated antigen family protein-D1 regulation of tumor cell migration,adhesion to endothelium,and actin structures reorganization in response to hypoxic stress[J].Cell Commun Adhes,2007,14(1):21-31. 被引量:1
  • 10SHEN Weigan,PENG Wanxin,SHAO Yue,et al.Localization and activity of calmodulin is involved in cell-cell adhesion of tumor cells and endothelial cells in response to hypoxic stress[J].Cell Biol Toxicol,2007,23(5):323-335. 被引量:1

引证文献3

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部