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克栓酶抑瘤作用的实验研究[J]. 肿瘤防治研究, 2000, 27(04): 256-259. DOI: 10.3971/j.issn.1000-8578.1308
引用本文: 克栓酶抑瘤作用的实验研究[J]. 肿瘤防治研究, 2000, 27(04): 256-259. DOI: 10.3971/j.issn.1000-8578.1308
Observed the Inhibitory Tumor Effdct of Batroxobin[J]. Cancer Research on Prevention and Treatment, 2000, 27(04): 256-259. DOI: 10.3971/j.issn.1000-8578.1308
Citation: Observed the Inhibitory Tumor Effdct of Batroxobin[J]. Cancer Research on Prevention and Treatment, 2000, 27(04): 256-259. DOI: 10.3971/j.issn.1000-8578.1308

克栓酶抑瘤作用的实验研究

Observed the Inhibitory Tumor Effdct of Batroxobin

  • 摘要: 目的 实验研究克栓酶的抑瘤作用,以期扩展其药用范围,为治疗肿瘤增加药源。方法 采用双层琼脂培养,流式细胞检测,免疫组化图象分析,MTT-ELISA等,以及荷瘤裸鼠整体实验方法观察对人肺癌细胞(PG)与正常人胚内皮细胞增殖抑制作用。结果 证明克栓梅可抑制PG与人胚内皮细胞增殖,具有统计学意义。结论 克栓酶毒性低具有治疗肿瘤的潜能。在肿瘤综合治疗中如何合理联合配伍使用克栓酶值得进一步探讨。

     

    Abstract: Objective To research the Batroxobin DF-521 effect on inhibition of tumor in order to extend its useful range and provide a new drug for curing tumor. Methods To observe the Batroxobin DF-521 effect on human lung cancer cell line PG and normal human embryo vasculo-endothelia cell using double layer agar culture,fluorecetometry,immunohisto chemical immage analysis,MTT-ELISA and inhibitory tumor test with nude mice. Results The Batroxobin was able to inhibit amplification of PG and vasculo-endothelia cells. Conclusion The Batroxobin is a low toxicial drug and has potential in curing tumor.It is worth to explore further how to appropriately use the Batroxobin with other drugs in tumor synthetical treatment.

     

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