期刊文献+

Effect of non-anticoagulant N-desulfated heparin on expression of vascular endothelial growth factor, angiogenesis and metastasis of orthotopic implantation of human gastric carcinoma 被引量:6

Effect of non-anticoagulant N-desulfated heparin on expression of vascular endothelial growth factor, angiogenesis and metastasis of orthotopic implantation of human gastric carcinoma
在线阅读 下载PDF
导出
摘要 AIM: To investigate the effect of N-desulfated heparin on tumor metastasis and angiogenesis, and expression of vascular endothelial growth factor (VEGF) of orthotopic implantation of human gastric carcinoma in male severe combined immune deficiency (SCID) mice. METHODS: Human gastric cancer SGC-7901 cells were orthotopically implanted into the stomach of SC/D mice. The mice were randomly divided into normal saline group and N-desulfated heparin group. One week after operation, the mice in N-desulfated heparin group reo ceived i.v. injections of N-desulfated heparin (Shanghai Institute of Cell Biology, Chinese Academy of Sciences, 10 mg/kg.d) twice weekly for 3 wk. The mice in normal saline group received i.v. injections of normal saline (100 μL) twice weekly for 3 wk. The mice were sacrificed six weeks after implantation. Tumor metastasis was evaluo ated histologically for metastasis under microscope. Intratumoral microvessel density (MVD) and VEGF expression were evaluated immuohistochemically. VEGF mRNA expression in gastric tissue of SC/D mice was detected by real time PCR. RESULTS: The tumor metastasis rate was 80% in normal saline group and 20% in N-desulfated heparin group (P 〈 0.05). MVD was 8.0 ± 3.1 in normal saline group and 4.3 ± 1.8 in N-desulfated heparin group (P 〈 0.05). VEGF positive immunostaining was found in cytoplasm of cancer cells. The rate of VEGF positive expression was higher in normal saline group than in N-desulfated hepa- rin treated group (90% vs 20%, P 〈 0.05). VEGF mRNA expression was significantly inhibited by N-desulfated heparin and was higher in normal saline group than in N-desulfated heparin group (Ct value 19.51 ± 1.01 vs 22.55± 1.36, P 〈 0.05). N-desulfated heparin significantly inhibited the expression of VEGF mRNA in cancer cells. No bleeding occurred in N-desulfated heparin group. CONCLUSION: N-desulfated heparin can inhibit metastasis of gastric cancer by suppressing tumor VEGF expression and tumor angiogenesis, but has no obvious anticoagulant activity. AIM: To investigate the effect of N-desulfated heparin on tumor metastasis and angiogenesis, and expression of vascular endothelial growth factor (VEGF) of ortho- topic implantation of human gastric carcinoma in male severe combined immune deficiency (SCID) mice.? METHODS: Human gastric cancer SGC-7901 cells were orthotopically implanted into the stomach of SCID mice.? The mice were randomly divided into normal saline group and N-desulfated heparin group.? One week after operation, the mice in N-desulfated heparin group re- ceived i.?v.? injections of N-desulfated heparin (SShhaanngghhaaii Institute of Cell Biology, Chinese Academy of Sciences, 10 mg/kg.?d)) ttwwiiccee wweeeekkllyy ffoorr ???? wwkk..?? ??hhee mmiiccee iinn nnoorrmmaall saline group received i.?v.? injections of normal saline (100 μL) twice weekly for ?? wk.? ?he mice were sacrificed six weeks after implantation.? ?umor metastasis was evalu- ated histologically for metastasis under microscope.? In- tratumoral microvessel density (MVD) and VEGF expres- sion were evaluated immuohistochemically.? VVVEEEGGGFFF mmmRR?NNNAAA expression in gastric tissue of SCID mice was detected by real time PC?.? RESULTS: The tumor metastasis rate was 80% in nor- mal saline group and 20% in N-desulfated heparin group (P ???? 00..??00??))..?? MMVVDD wwaass ??..??00 ???? ????..??11 iinn nnoorrmmaall ssaalliinnee ggrroouupp and 4.??? ?? 1.?? in N-desulfated heparin group (P ???? 00..??00??))..?? VEGF positive immunostaining was found in cytoplasmof cancer cells.? ?he rate of VEGF positive expression was higher in normal saline group than in N-desulfated hepa- rin treated group (90% vs 20%, P ???? 00..??00??))..?? VVEEGGFF mm??NNAA expression was significantly inhibited by N-desulfated heparin and was higher in normal saline group than in N-desulfated heparin group (Ct value 19.??1 ?? 1.?01 vs 22.??? ?? 1.???6, P ???? 00..??00??))..?? NN--ddeessuullffaatteedd hheeppaarriinn ssiiggnniiffii- cantly inhibited the expression of VEGF mRNA in can- cer cells.? No bleeding occurred in N-desulfated heparin group.? CONCLUSION: N-desulfated heparin can inhibit me- tastasis of gastric cancer by suppressing tumor VEGF expression and tumor angiogenesis, but has no obvious anticoagulant activity.?
出处 《World Journal of Gastroenterology》 SCIE CAS CSCD 2007年第3期457-461,共5页 世界胃肠病学杂志(英文版)
基金 Supported by the Scientific Foundation of Shanghai Public Health Administration, No.034045
关键词 N-desulfated heparin Gastric carcinoma METASTASIS Tumor angiogenesis Vascular endothelial growth factor 胃癌 肿瘤 血管发生 细胞转移
作者简介 Correspondence to: Jin-Lian Chen, Department of Gastroenterology, Shanghai Sixth People's Hospital, Shanghai Jiaotong University, Shanghai 200233, China. wqq-021002@163.com Telephone: +86-21-64369181 Fax: +86-21-64369181
  • 相关文献

参考文献2

二级参考文献12

  • 1Yan Xin,Xiao Ling Li,Yan Ping Wang,Su Min Zhang,Hua Chuan Zheng,Dong Ying Wu,Yin Chang Zhang The Fourth Laboratory of Cancer Institute, China Medical University, Shenyang 110001, Liaoning Province, China.Relationship between phenotypes of cell-function differentiation and pathobiological behavior of gastric carcinomas[J].World Journal of Gastroenterology,2001,7(1):53-59. 被引量:39
  • 2Kojima N,Sato M,Suzuki A,Sato T,Satoh S,Kato T,Senoo H.Enhanced expression of B7-1,B7-2,and intercellular adhesion molecule 1 in sinusoidal endothelial cells by warm ischemia/reperfusion injury in rat liver[].Hepatology.2001
  • 3Nemoto T,Burne MJ,Daniels F,O‘Donnell MP,Crosson J,Berens K,Issekutz A,Kasiske BL,Keane WF,Rabb H.Small molecule selectin ligand inhibition improves outcome in ischemic acute renal failure[].Kidney International.2001
  • 4Downey P,Tolley DA,Johnston SR,Young M.Ischemiareperfusion injury after relief of ureteral obstruction:an animal study[].Journal of Endourology.2001
  • 5Thorlacius H,Zhang XW.P-selectin-mediated rolling is a prerequisite for ICAM-1-independent firm adhesion in arterioles provoked by tumor necrosis factor-alpha in vivo[].Microvascular Research.1999
  • 6Sache E,Maillard M,Malazzi P,Bertrand H.Partially Ndesulfated heparin as a non-anticoagulant heparin:some physico-chemical and biological properties[].Thrombosis Research.1989
  • 7Kuzume,M,Nakano,H,Yamaguchi,M,Matsumiya,A,Shimokohbe,G,Kitamura,N,Nagasaki,H,Kumada,K.A monoclonal antibody against ICAM-1 suppresses hepatic ischemia-reperfusion injury in rats[].European Surgical Research.1997
  • 8Yadav SS,Howell DN,Gao W,et al.L-selectin and ICAM-1 mediate reperfusion injury and neutrophil adhesion in the warm ischemic mouse liver[].American Journal of Physiology.1998
  • 9Colletti LM,Cortis A,Lukacs N,Kunkel SL,Green M,Strieter RM.Tumor necrosis factor up-regulates intercellular adhesion molecule 1, which is important in the neutrophil-dependent lung and liver injury associated with hepatic ischemia and reperfusion in the rat[].Shock.1998
  • 10Meyer K,Brown MF,Zibari G,Panes J,McMillan RW,McDonald JC,Granger DN.ICAM-1 upregulation in distant tissues after hepatic ischemia/reperfusion: a clue to the mechanism of multiple organ failure[].Journal of Pediatric Surgery.1998

共引文献28

同被引文献59

引证文献6

二级引证文献34

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