期刊文献+

Surgetake^(TM)间皮组织细胞极性修复与癌细胞抑制实验研究 被引量:3

Surgitake^(TM) for repair of mesothelium polarity and cancer cell inhibition:an experimental study
下载PDF
导出
摘要 目的探讨间皮组织细胞极性修复对癌细胞生长抑制的影响。方法分别采用细胞极性修复实验、消化道吻合口愈合影响实验、"T"管窦道形成实验、细胞极性修复相关指标检测、永生化细胞(人膀胱癌细胞株T24)抑制实验等一系列从动物实验到细胞实验,采用SurgetakeTM或生理盐水进行了对照研究。结果兔实验结果显示,实验组10例均实现极性修复,而对照组均无完全实现极性修改;同时实验表明SurgetakeTM具有较强的激活体内t-PA的活性,用药后实验组t-PA达到(1.6±0.8)IU/ml,而对照组t-PA为(0.9±0.4)IU/ml,两组比较差异有统计学意义(P<0.01)。永生化细胞(人膀胱癌细胞株T24)抑制实验实验结果显示surgetakeTM组3个视野计数细胞总数为844个,对照组3个视野细胞总数为2295个。结论 SurgetakeTM具有保持间皮组织极性的作用,实现了间皮结构的重建,能使t-PA增加,细胞极性增强,组织修复的就好。细胞的极性保持过程与小分子蛋白t-PA相关,这一过程的极化作用可使肿瘤细胞恶性程度降低。 Objective To determine the effects of repair of mesothelium polarity on cancer cell inhibition.Methods Serial animal and cytological experiments,including cell polarity repair test,alimentary tract anastamosis healing test,T-tube fistula formation test,assessment of the parameters associated with cellular polarity repair and immortal cell(human bladder cancer cell line T24) inhibition,were employed in the control trials by using Surgetake^TM and normal saline.Results The experiments on rabbits evidenced a markedly higher proportion of complete repair of cellular polarity in SurgetakeTM group(n=10) than that in control group(P〈0.01).Surgetake^TM more potently potentiated the t-PA activity in vivo [(1.6±0.8)IU/ml vs(0.9±0.4)IU/ml],P〈0.01) and yielded a higher cell count in three visual fields when compared with normal controls(2995 vs 844,P〈0.05),as evidenced by immortalized cell inhibition test.Conclusion Surgetake^TM achieves mesothelium reconstruction by retaining tissue polarity and benefits the tissue repair from elevated t-PA activity leading to potentiated cellular polarity.The fact that maintenance of polarity correlate considerably with t-PA,a low molecular weight protein,indicates reduced malignancy via cellular polarization.
出处 《中国药物与临床》 CAS 2013年第1期5-8,I0001,共5页 Chinese Remedies & Clinics
基金 国家九五攻关项目"国家十项新药与产业化"课题子项目(9690105159)
关键词 上皮 肿瘤 组织 Epithelium Neoplasm Histiocytes
  • 相关文献

参考文献2

二级参考文献5

  • 1Robert F,Buckman CTP,Monty MC,et al.Unifying pathogenetic mechanism in the etiology of intraperitoneal edhesions.J Surg Res,1976,20:1-5.
  • 2Evans DM,McAree K,Guyton DP,et al.Dose dependency and wound healing aspects of the use of tissue plasminogen activator in the prevention of intra-abdominal adhesions.Am J Surg,1993,165:229-232
  • 3Gervin AS,Pnekett CL,Silver D.Seresal hypofibfinolysis a cause of postoperative adhesions.Am J Surg,1973,125:80-88.
  • 4Reed KI,Stuccbi AF,Beeker JM.Pharmacologic inhibition of adhesion formation and peritoneal tissue-type plasminogen activator activity.Semin Reprad Med,2008,26(4):331-340.
  • 5Reed KL,Stucchi AF,Leeman SE,et al.Inhibitory effects of a neurokinin-1 receptor antagonist on postoperative peritoneal adhesion formation.Ann N Y Acad Sci,2008,1144:116-126.

共引文献4

同被引文献5

引证文献3

二级引证文献5

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