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

机译:非抗凝N-脱硫肝素对人胃癌原位移植血管内皮生长因子表达,血管生成和转移的影响

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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 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 received 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 evaluated histologically for metastasis under microscope. Intratumoral microvessel density (MVD) and VEGF expression were evaluated immuohistochemically. VEGF mRNA expression in gastric tissue of SCID 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 heparin 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.
机译:目的:探讨N-脱硫肝素对雄性重症联合免疫缺陷(SCID)小鼠原位移植人胃癌的肿瘤转移和血管生成以及血管内皮生长因子(VEGF)表达的影响。方法:将人胃癌SGC-7901细胞原位植入SCID小鼠的胃中。将小鼠随机分为生理盐水组和N-脱硫肝素组。手术一周后,N-脱硫肝素组的小鼠接受了静脉注射。每周两次注射N-脱硫肝素(中国科学院上海细胞生物学研究所,10 mg / kg.d),连续3周。生理盐水组的小鼠接受静脉注射。每周两次注射生理盐水(100μL),每周3周。植入六周后处死小鼠。在显微镜下组织学评价肿瘤转移的转移。免疫组织化学法评价肿瘤内微血管密度(MVD)和VEGF表达。实时荧光定量PCR检测SCID小鼠胃组织中VEGF mRNA的表达。结果:生理盐水组肿瘤转移率为80%,N-脱硫肝素组肿瘤转移率为20%(P <0.05)。生理盐水组的MVD为8.0±3.1,N-脱硫肝素组的MVD为4.3±1.8(P <0.05)。在癌细胞的细胞质中发现了VEGF阳性的免疫染色。生理盐水组的VEGF阳性表达率高于N-脱硫肝素治疗组(90%vs 20%,P <0.05)。 N-脱硫肝素可显着抑制VEGF mRNA的表达,并且在生理盐水组中高于N-脱硫肝素组(Ct值19.51±1.01 vs 22.55±1.36,P <0.05)。 N-脱硫肝素显着抑制癌细胞中VEGF mRNA的表达。 N-脱硫肝素组无出血发生。结论:N-脱硫肝素可通过抑制肿瘤VEGF的表达和血管新生而抑制胃癌的转移,但无明显的抗凝活性。

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